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Nivolumab in Patients With IDH-Mutant Gliomas With and Without Hypermutator Phenotype

Phase II Trial Evaluating Nivolumab In Patients With IDH-Mutant Gliomas With And Without Hypermutator Phenotype

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03718767
Enrollment
62
Registered
2018-10-24
Start date
2019-03-27
Completion date
2026-11-30
Last updated
2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glioblastoma, Glioma, High Grade Glioma, Low Grade Glioma, Malignant Glioma

Keywords

PD 1 Pathway, High Tumor Mutational Load, Immune Checkpoint, Quality of Life

Brief summary

Background: Gliomas are the most common malignant brain tumors. Some have certain changes (mutations) in the genes isocitrate dehydrogenase 1 (IDH1) or isocitrate dehydrogenase 2 (IDH2). If there are a high number of mutations in a tumor, it is called hypermutator phenotype (HMP). The drug nivolumab helps the immune system fight cancer. Researchers think it can be more effective in patients with IDH1 or IDH2 mutated gliomas with HMP. They will test gliomas with and without HMP. Objectives: To see if nivolumab stops tumor growth and prolongs the time that the tumor is controlled. Eligibility: Adults 18 years or older with IDH1 or IDH2 mutated gliomas Design: Participants will be screened with: Medical history Physical exam Heart, blood, and pregnancy tests Review of symptoms and activity levels Brain magnetic resonance imaging (MRI). Participants will lie in a cylinder that takes pictures in a strong magnetic field. Tumor samples Participants will get the study drug in 4-week cycles. They will get it through a small plastic tube in a vein (intravenous \[IV\]) on days 1 and 15 of cycles 1-4. For cycles 5-16, they will get it just on day 1. On days 1 and 15 of each cycle, participants will repeat some or all screening tests. After cycle 16, participants will have 3 follow-up visits over 100 days. They will answer health questions, have physical and neurological exams, and have blood tests. They may have a brain MRI. Participants whose disease did not get worse but who finished the study drug within 1 year of treatment may have imaging studies every 8 weeks for up to 1 year. Participants will be called or emailed every 6 months with questions about their health.

Detailed description

BACKGROUND: * Glioma is the most common malignant brain tumor. Genes coding for isocitrate dehydrogenases 1and 2 (IDH1 and IDH2), metabolic enzymes, are frequently mutated in gliomas, particularly lower-grade gliomas (LGGs). IDH1/2 mutation causes a unique tumor biology, including the accumulation of 2-hydroxyglutarate (2-HG), an oncometabolite, which in turn causes genomic hypermethylation and tumorigenesis. * IDH-mutant LGGs undergo a slow but unremitting progression to higher grade transformation (HT) and eventually become high grade gliomas (HGGs) with a significant increase in the number of somatic mutations. A subset of patients with transformed HGGs develop a hypermutator phenotype (HMP), possibly related, but not limited, to previous treatment with alkylating agents and radiotherapy. The mechanisms of this clinical phenomenon are not fully understood, and no effective treatments are available for the HMP HGGs. * High tumor mutation burden (TMB) is a characteristic finding in many of the transformed tumors. Furthermore, this increased mutation burden, with commensurate increase in neoantigen expression, may be correlated with a better response to immune checkpoint inhibitor (ICPIs) treatment. * Nivolumab is a monoclonal antibody that binds to the programmed cell death protein 1 (PD1) receptor and blocks its interaction with programmed death-ligand 1 (PD L1) and PD L2 and subsequently releasing PD 1 pathway mediated inhibition of the immune response, including antitumor immune response. * The United States (US) Food and Drug Administration granted approval to nivolumab for the treatment of unresectable or metastatic melanoma, advanced non-small cell lung cancer, renal cell carcinoma, Hodgkin's lymphoma, recurrent or metastatic squamous cell carcinoma of the head and neck, locally advanced or metastatic urothelial carcinoma, microsatellite instability-high or mismatched repair deficient metastatic colorectal cancer and hepatocellular carcinoma. * The first randomized clinical trial in glioblastoma with nivolumab (CheckMate-143) was completed in early 2017. Unfortunately, the study didn't meet its primary endpoint of improved overall survival over bevacizumab monotherapy. The objective response rate (ORR) was lower in nivolumab arm than bevacizumab arm. However, the response with nivolumab was more durable. The safety profile of nivolumab was very consistent with what has been observed in other tumor types. OBJECTIVE: -To determine the 6-month progression free survival rate in IDH-mutant gliomas patients with and without HMP in responses to nivolumab treatment. ELIGIBILITY: * Patients with diffuse glioma, confirmed by National Cancer Institute (NCI) Laboratory of Pathology * Age greater than or equal to 18 years * Karnofsky Performance Scale (KPS) greater than or equal to 60% * IDH 1 or IDH 2 mutation confirmed by deoxyribonucleic acid (DNA) sequencing * Patients must have TMB status performed at National Institutes of Health (NIH) * Tumor tissue or slides should be available for molecular and immune profiling DESIGN: * This study is an open label phase II clinical trial of the immune checkpoint inhibitor, nivolumab, in patients with HMP and non-hypermutated phenotype (NHMP) IDH-mutant gliomas. * Patients with HMP and NHMP will receive nivolumab at a standard dose of 240 mg intravenously every 2 weeks for cycles 1-2, then doses of 480 mg every 4 weeks for cycles 3-16. A maximum of 20 treatments will be given (16 cycles). * A maximum of 29 patients with IDH-mutant glioma with HMP (Cohort 1) and 30 patients with NHMP (Cohort 2) will be evaluated. * A Simon's optimal two-stage design will be used to conduct the HMP arm and the NHMP arm independently. For the HMP cohort, in stage I, a total number of 10 patients are accrued. If 9 or more patients progress by 6 months, the cohort will be terminated early; otherwise, additional 19 patients will be accrued in stage II, resulting in a total sample size of 29. Among these 29 patients, if 6 or more patients are progression-free at 6 months, we will claim that the treatment is promising for patients with HMP IDH-mutant gliomas. For NHMP cohort, in stage I, a total number of 15 patients are accrued. If 3 or more patients are progression-free at 6 months, the cohort will move to stage II and an additional 15 patients will be accrued in stage II, resulting in a total sample size of 30. Among these 30 patients, if 10 or more patients are progression-free at 6 months, we will claim that the treatment is promising for patients with NHMP IDH-mutant gliomas.

Interventions

DRUGNivolumab

Intravenous (IV) Nivolumab

Sponsors

National Cancer Institute (NCI)
Lead SponsorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* INCLUSION CRITERIA: * Patients must have recurrent diffuse glioma (histologically confirmed by National Institutes of Health (NIH) Laboratory of Pathology) with isocitrate dehydrogenase 1 (IDH1) or isocitrate dehydrogenase 2 (IDH2) mutation (confirmed by deoxyribonucleic acid (DNA) sequencing, Foundation One is preferable for confirmation of mutation, but not necessary). * Patients must have tumor specific mutation burden (number of somatic mutations per exome) tested at NIH: Must have either result of tumor mutation burden from the most recent surgical tumor sample or must provide adequate genomic materials of the sample for tumor testing. The tumor tissue (e.g., block or 15 unstained slides) must be available for molecular and immune profiling. Fresh or frozen tumor sample will be used if available, but not mandatory. * Age greater than or equal to 18 years. Because no dosing or adverse event data are currently available on the use of nivolumab in patients \<18 years of age, children are excluded from this study but will be eligible for future pediatric trials. * Patient must be able to tolerate a magnetic resonance imaging (MRI) study with intravenous gadolinium contrast. * Karnofsky greater than or equal to 60% * Patients must have adequate organ and marrow function as defined below: * Absolute neutrophil count greater than or equal to 1,500/mcL * Platelet Count greater than or equal to 100,000/MCL * Hemoglobin greater than 9.0 g/dL (may be transfused to achieve this level) * Blood Urea Nitrogen (BUN) less than or equal to 30 mg/dL and * Serum creatinine less than or equal to 1.7 mg/dL * Total bilirubin (except patients with Gilbert's Syndrome, who are eligible for the study but exempt from the total bilirubin eligibility criterion) less than or equal to 2.0 mg/dL * Alanine aminotransferase (ALT) and aspartate aminotransaminase (AST) less than or equal to 2.5x institutional upper limit of normal. * The effects of nivolumab on the developing human fetus are unknown. For this reason, women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation and up to 5 months (women). Should a woman become pregnant or suspect she is pregnant while she is participating in this study, she should inform her treating physician immediately. * The patient must be able to understand and be willing to sign a written informed consent document.

Exclusion criteria

* Patients who are receiving any other investigational agents. * Patients who have a history of receiving immune therapy. * History of allergic reactions attributed to compounds of similar chemical or biologic composition to nivolumab. * History of severe hypersensitivity reaction to any monoclonal antibody. * Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years prior to initiation of study therapy. * Patients with active autoimmune disease or history of autoimmune disease that might recur, which may affect vital organ function or require immune suppressive treatment including systemic corticosteroids. These include but are not limited to patients with a history of immune related neurologic disease, multiple sclerosis, autoimmune (demyelinating) neuropathy, Guillain-Barre syndrome or Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), myasthenia gravis; systemic autoimmune disease such as Systemic Lupus Erythematosus (SLE), connective tissue diseases, scleroderma, inflammatory bowel disease (IBD), Crohn's, ulcerative colitis, hepatitis; and patients with a history of toxic epidermal necrolysis (TEN), Stevens-Johnson syndrome, or phospholipid syndrome. Such diseases should be excluded because of the risk of recurrence or exacerbation of disease. --Of note, patients with vitiligo, endocrine deficiencies including thyroiditis managed with replacement hormones including physiologic corticosteroids are eligible. Patients with rheumatoid arthritis and other arthropathies, Sjogren's syndrome and psoriasis controlled with topical medication and patients with positive serology, such as antinuclear antibodies (ANA), anti-thyroid antibodies should be evaluated for the presence of target organ involvement and potential need for systemic treatment but should otherwise be eligible. * The patient must not be currently on a corticosteroid dose greater than dexamethasone 1 mg per day or its equivalent. * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations (within timeframes identified in the bullets below) that would limit compliance with study requirements. * Known human immunodeficiency virus (HIV)-positive or acquired immune deficiency syndrome (AIDS) based upon current Centers for Disease Control and Prevention (CDC) definition; note, however, that HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS is based on the lack of information regarding the safety of nivolumab in patients with active HIV infection * Pregnant women are excluded from this study because nivolumab's potential for teratogenic or abortifacient effects is unknown. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with nivolumab, breastfeeding should be discontinued if the mother is treated with nivolumab.

Design outcomes

Primary

MeasureTime frameDescription
Median Progression Free Survival (PFS) Rate at 6 Months6 monthsPFS is defined from the day of study entry until imaging is confirmed to show disease progression or death, whichever occurs first. Disease progression was assessed by the Immunotherapy Response Assessment neuro-oncology Criteria. Disease progression is \>25% increase in sum of the products of perpendicular diameters of enhancing lesions; any new enhancing measurable lesion that exceeds a 25% increase in cross-sectional area; clear clinical deterioration not attributable to other causes apart from the tumor and/or failure to return for evaluation due to death or deteriorating condition. PFS was analyzed by the Kaplan-Meier method and is reported with a 95% confidence interval.

Secondary

MeasureTime frameDescription
Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Baseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).Participant reported outcome measures using self-reported symptom interference with daily activities using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT). The MDSAI-BT 5-minute questionnaire uses an 11-point scale (0-10) to rate symptoms interference in the last 24 hours of a participant's life related to mood, work Inside and outside the home), relations with other people, walking and enjoyment of life. 0 = symptom not present and 10 = as bad as you can imagine. Higher score indicates more interference. Per protocol, MDSAIs are performed with imaging. If no imaging, no MDASI.
Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Baseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).Participant reported outcome measures using self-reported symptom severity with daily activities (e.g., work) using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) are reported for each treatment cycle. The MDSAI-BT 5-minute questionnaire uses an 11-point Likert scale (0-10). 0 = symptom not present and 10 = as bad as you can imagine. Higher score indicates worse severity. Per protocol, MDSAIs are performed with imaging. If no imaging, no MDASI.
Overall SurvivalUntil the death of the last surviving participant, a median of 7.4 months in Cohort 1 and a median of 31.6 months in Cohort 2.OS is defined as the time from treatment initiation to the time of death.
Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Baseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).The proportion of participants rating symptoms 5 or greater (on a 0-10 scale) was assessed using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT). The MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) 5-minute questionnaire uses an 11-point Likert scale (0-10) to measure symptoms reported by the participant. 0 = symptom not present and 10 = as bad as you can imagine. Higher score indicates worse severity.
Median Percentage of Participants That Have Progressive Disease At 12 MonthsAt 12 monthsPFS was analyzed by the Kaplan-Meier method and is reported with a 95% confidence interval. PFS is defined from the day of study entry until imaging is confirmed to show disease progression. Disease progression was assessed by the Immunotherapy Response Assessment neuro-oncology Criteria. Disease progression is \>25% increase in sum of the products of perpendicular diameters of enhancing lesions; any new enhancing measurable lesion that exceeds a 25% increase in cross-sectional area; clear clinical deterioration not attributable to other causes apart from the tumor and/or failure to return for evaluation due to death or deteriorating condition.
Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsBaseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).Here is the number of participants with IDH-mutant gliomas with and without hypermutator phenotype, responses received and were expected using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) forms. Received MDASI-BT forms will be checked versus the timing schedule and considered as valid if they fall within ten days of the scheduled assessment window. Compliance rates will be calculated as the number of received valid forms over the number of expected forms.
Tumor Mutation BurdenDuring the screening period (14 days prior to study therapy)Tumor mutation Burden is measured using whole exome sequencing.

Other

MeasureTime frameDescription
Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0)From the first study intervention, Study Day 1 of Cycle 1 through 30 days after the study agent (s) was/were administered, up to 17 monthsHere is the number of participants with serious and/or non-serious adverse events assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned.

Countries

United States

Participant flow

Participants by arm

ArmCount
Cohort 1/Hypermutated Phenotype (HMP)
Isocitrate dehydrogenase (IDH) - mutant gliomas participants with hypermutated phenotype (HMP). Participants received Nivolumab 240mg every (q)2 weeks in Cycle 1 - Cycle 2 and then 480mg q4 weeks in Cycle 3-Cycle 16.
8
Cohort 2/Non-hypermutated Phenotype (NHMP).
Isocitrate dehydrogenase (IDH) - mutant gliomas participants with non-hypermutated phenotype (NHMP). Participants received Nivolumab 240mg every (q)2 weeks in Cycle 1 - Cycle 2 and then 480mg q4 weeks in Cycle 3-Cycle 16.
30
Enrolled But Not Treated
Participants were enrolled, not assigned to Cohorts/Arms and not treated.
24
Total62

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyDeclined to participate (before treatment started)007
Overall StudyIneligible0017

Baseline characteristics

CharacteristicCohort 1/Hypermutated Phenotype (HMP)Cohort 2/Non-hypermutated Phenotype (NHMP).Enrolled But Not TreatedTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants2 Participants0 Participants2 Participants
Age, Categorical
Between 18 and 65 years
8 Participants28 Participants24 Participants60 Participants
Age, Continuous44.38 years
STANDARD_DEVIATION 11.7
45.27 years
STANDARD_DEVIATION 11.68
40.5 years
STANDARD_DEVIATION 10.19
43.31 years
STANDARD_DEVIATION 11.17
Race/Ethnicity, Customized
Ethnicity: Hispanic or Latino
8 Participants4 Participants1 Participants13 Participants
Race/Ethnicity, Customized
Ethnicity: Not Hispanic or Latino
0 Participants26 Participants23 Participants49 Participants
Race/Ethnicity, Customized
Ethnicity: Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Race: American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Race: Asian
0 Participants5 Participants0 Participants5 Participants
Race/Ethnicity, Customized
Race: Black or African American
0 Participants1 Participants2 Participants3 Participants
Race/Ethnicity, Customized
Race: More than one race
0 Participants0 Participants1 Participants1 Participants
Race/Ethnicity, Customized
Race: Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Race: Other
0 Participants1 Participants0 Participants1 Participants
Race/Ethnicity, Customized
Race: Unknown or Not Reported
0 Participants2 Participants00 Participants2 Participants
Race/Ethnicity, Customized
Race: White
8 Participants21 Participants21 Participants50 Participants
Region of Enrollment
United States
8 participants30 participants24 participants62 participants
Sex: Female, Male
Female
5 Participants10 Participants6 Participants21 Participants
Sex: Female, Male
Male
3 Participants20 Participants18 Participants41 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
6 / 816 / 30
other
Total, other adverse events
7 / 826 / 30
serious
Total, serious adverse events
3 / 811 / 30

Outcome results

Primary

Median Progression Free Survival (PFS) Rate at 6 Months

PFS is defined from the day of study entry until imaging is confirmed to show disease progression or death, whichever occurs first. Disease progression was assessed by the Immunotherapy Response Assessment neuro-oncology Criteria. Disease progression is \>25% increase in sum of the products of perpendicular diameters of enhancing lesions; any new enhancing measurable lesion that exceeds a 25% increase in cross-sectional area; clear clinical deterioration not attributable to other causes apart from the tumor and/or failure to return for evaluation due to death or deteriorating condition. PFS was analyzed by the Kaplan-Meier method and is reported with a 95% confidence interval.

Time frame: 6 months

Population: 38/62 participants are reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureValue (NUMBER)
Cohort 1/Hypermutated Phenotype (HMP)Median Progression Free Survival (PFS) Rate at 6 Months25.0 Percentage of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Median Progression Free Survival (PFS) Rate at 6 Months40.0 Percentage of participants
Secondary

Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)

Participant reported outcome measures using self-reported symptom interference with daily activities using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT). The MDSAI-BT 5-minute questionnaire uses an 11-point scale (0-10) to rate symptoms interference in the last 24 hours of a participant's life related to mood, work Inside and outside the home), relations with other people, walking and enjoyment of life. 0 = symptom not present and 10 = as bad as you can imagine. Higher score indicates more interference. Per protocol, MDSAIs are performed with imaging. If no imaging, no MDASI.

Time frame: Baseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).

Population: 38/62 participants were reported because 7 declined to participate (before treatment started) and 17 were ineligible. Reasons data not reported in Cycles: participants came off treatment due to disease progression or toxicity, refused further treatment, did not complete the questionnaire, did extra MDASI because of short-interval imaging, refused to complete MDASI (no computer), data collected but not captured in database for a participant, and MDSAI not done related to outside hospitalization.

ArmMeasureGroupValue (MEAN)Dispersion
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Baseline3.96 score on a scaleStandard Deviation 2.96
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 23.21 score on a scaleStandard Deviation 2.67
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 42.33 score on a scaleStandard Deviation 1.99
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 62.42 score on a scaleStandard Deviation 3.42
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 83.00 score on a scaleStandard Deviation 4
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 104.17 score on a scaleStandard Deviation 5.42
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 124.25 score on a scaleStandard Deviation 6.01
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 144.83 score on a scaleStandard Deviation 6.36
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 121.00 score on a scaleStandard Deviation 1.28
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 82.46 score on a scaleStandard Deviation 2.03
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Baseline2.06 score on a scaleStandard Deviation 2.8
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 160.57 score on a scaleStandard Deviation 1.27
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 22.30 score on a scaleStandard Deviation 2.35
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 101.45 score on a scaleStandard Deviation 1.43
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 42.19 score on a scaleStandard Deviation 2.07
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 141.17 score on a scaleStandard Deviation 1.59
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Interference Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 62.41 score on a scaleStandard Deviation 2.06
Secondary

Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)

Participant reported outcome measures using self-reported symptom severity with daily activities (e.g., work) using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) are reported for each treatment cycle. The MDSAI-BT 5-minute questionnaire uses an 11-point Likert scale (0-10). 0 = symptom not present and 10 = as bad as you can imagine. Higher score indicates worse severity. Per protocol, MDSAIs are performed with imaging. If no imaging, no MDASI.

Time frame: Baseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).

Population: 38/62 participants were reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureGroupValue (MEAN)Dispersion
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 122.70 score on a scaleStandard Deviation 3.7
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 142.41 score on a scaleStandard Deviation 3.34
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Baseline3.16 score on a scaleStandard Deviation 2.78
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 22.16 score on a scaleStandard Deviation 1.77
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 41.61 score on a scaleStandard Deviation 1.31
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 62.00 score on a scaleStandard Deviation 2.57
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 81.91 score on a scaleStandard Deviation 2.57
Cohort 1/Hypermutated Phenotype (HMP)Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 102.07 score on a scaleStandard Deviation 2.8
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 81.20 score on a scaleStandard Deviation 1.25
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 41.50 score on a scaleStandard Deviation 1.23
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 120.97 score on a scaleStandard Deviation 0.97
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 140.74 score on a scaleStandard Deviation 0.51
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 160.72 score on a scaleStandard Deviation 0.81
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 61.26 score on a scaleStandard Deviation 1.12
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Baseline4.16 score on a scaleStandard Deviation 1.56
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 100.82 score on a scaleStandard Deviation 0.7
Cohort 2/Non-hypermutated Phenotype (NHMP).Mean Symptom Severity Score Per Treatment Cycle Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Cycle 21.48 score on a scaleStandard Deviation 1.29
Secondary

Median Percentage of Participants That Have Progressive Disease At 12 Months

PFS was analyzed by the Kaplan-Meier method and is reported with a 95% confidence interval. PFS is defined from the day of study entry until imaging is confirmed to show disease progression. Disease progression was assessed by the Immunotherapy Response Assessment neuro-oncology Criteria. Disease progression is \>25% increase in sum of the products of perpendicular diameters of enhancing lesions; any new enhancing measurable lesion that exceeds a 25% increase in cross-sectional area; clear clinical deterioration not attributable to other causes apart from the tumor and/or failure to return for evaluation due to death or deteriorating condition.

Time frame: At 12 months

Population: 38/62 participants were reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureValue (NUMBER)
Cohort 1/Hypermutated Phenotype (HMP)Median Percentage of Participants That Have Progressive Disease At 12 Months25.0 Percentage of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Median Percentage of Participants That Have Progressive Disease At 12 Months33.3 Percentage of participants
Secondary

Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) Forms

Here is the number of participants with IDH-mutant gliomas with and without hypermutator phenotype, responses received and were expected using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) forms. Received MDASI-BT forms will be checked versus the timing schedule and considered as valid if they fall within ten days of the scheduled assessment window. Compliance rates will be calculated as the number of received valid forms over the number of expected forms.

Time frame: Baseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).

Population: 38/62 participants were reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 102 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 142 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 82 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 162 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 102 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 160 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 62 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at baseline8 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 122 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at baseline8 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 82 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 27 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 122 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 27 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 62 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 44 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 142 Participants
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 44 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 147 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 611 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 69 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 89 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 88 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 108 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 107 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 128 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 128 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 415 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 146 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 167 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 165 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at baseline30 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at baseline30 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 227 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsReceived at Cycle 225 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants Responses Received and Were Expected Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) FormsExpected at Cycle 416 Participants
Secondary

Overall Survival

OS is defined as the time from treatment initiation to the time of death.

Time frame: Until the death of the last surviving participant, a median of 7.4 months in Cohort 1 and a median of 31.6 months in Cohort 2.

Population: 38/62 participants are reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureValue (MEDIAN)
Cohort 1/Hypermutated Phenotype (HMP)Overall Survival7.4 Months
Cohort 2/Non-hypermutated Phenotype (NHMP).Overall Survival31.6 Months
Secondary

Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)

The proportion of participants rating symptoms 5 or greater (on a 0-10 scale) was assessed using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT). The MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT) 5-minute questionnaire uses an 11-point Likert scale (0-10) to measure symptoms reported by the participant. 0 = symptom not present and 10 = as bad as you can imagine. Higher score indicates worse severity.

Time frame: Baseline and Cycles 2, 4, 6, 8, 10, 12, 14, and 16 (approximately 32 weeks +/- 3 days).

Population: 38/62 participants were reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureGroupValue (NUMBER)
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.13 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.13 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.13 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.38 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.38 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.38 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.38 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.17 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.13 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.38 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.13 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.38 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.38 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP)Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.25 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.29 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.43 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.29 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.29 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.29 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.29 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.43 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.75 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.25 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.50 proportion of participants
Cohort 1/Hypermutated Phenotype (HMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.50 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.10 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.10 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.10 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.04 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.10 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.33 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.17 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.10 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.03 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.10 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.03 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.17 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - BaselineProportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.03 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.16 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.16 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.08 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.24 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.08 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.08 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.09 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.28 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.12 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.04 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.08 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.12 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.12 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.16 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.16 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 2Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.16 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.27 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.47 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.33 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.40 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.07 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 4Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.11 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.22 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.33 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.22 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.11 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.11 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.33 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.11 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.33 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.11 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.11 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 6Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.38 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.25 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.25 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.25 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 8Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.29 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.14 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 10Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.38 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.25 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.25 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.13 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 12Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.17 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.17 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.17 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.17 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.17 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 14Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling distressed0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling sad0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Shortness of breath0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Nausea0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty understanding0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Pain0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty concentrating0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty speaking0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Numbness/Tingling0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Rash0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Difficulty remembering0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Disturbed sleep0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in bowel pattern0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Irritability0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Feeling drowsy0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Dry mouth0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Lack of appetite0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Change in appearance0.40 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vomiting0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Fatigue0.40 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Weakness on one side of body0.20 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Seizure0.00 proportion of participants
Cohort 2/Non-hypermutated Phenotype (NHMP) - Cycle 16Proportion of Participants Rating Symptoms 5 or Greater (on a 0-10 Scale) Using the MD Anderson Symptom Inventory-Brain Tumor Module (MDSAI-BT)Vision0.20 proportion of participants
Secondary

Tumor Mutation Burden

Tumor mutation Burden is measured using whole exome sequencing.

Time frame: During the screening period (14 days prior to study therapy)

Population: 38/62 participants were reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureValue (MEAN)Dispersion
Cohort 1/Hypermutated Phenotype (HMP)Tumor Mutation Burden76.39 mutation/MbStandard Deviation 78.54
Cohort 2/Non-hypermutated Phenotype (NHMP).Tumor Mutation Burden1.28 mutation/MbStandard Deviation 0.61
p-value: 0.623Regression, Cox
p-value: 0.073Regression, Cox
Other Pre-specified

Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0)

Here is the number of participants with serious and/or non-serious adverse events assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned.

Time frame: From the first study intervention, Study Day 1 of Cycle 1 through 30 days after the study agent (s) was/were administered, up to 17 months

Population: 38/62 participants were reported because 7 declined to participate (before treatment started) and 17 were ineligible.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Cohort 1/Hypermutated Phenotype (HMP)Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0)7 Participants
Cohort 2/Non-hypermutated Phenotype (NHMP).Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0)26 Participants

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026