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Lymphocyte Re-infusion During Immune Suppression to Treat Metastatic Melanoma

Treatment of Patients With Metastatic Melanoma Using Cloned Lymphocytes Following the Administration of a Non-Myeloablative But Lymphocyte Depleting Regimen

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00001832
Enrollment
170
Registered
1999-11-04
Start date
1999-08-31
Completion date
2010-05-31
Last updated
2012-12-21

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

Conditions

Melanoma, Neoplasm Metastasis

Keywords

Immunotherapy, Adoptive Transfer, IL-2, Toxicity, Clinical Response, Breast Cancer

Brief summary

This experiment will test the safety and effectiveness of a treatment for melanoma in which certain lymphocytes (a type of white blood cell) are taken from the patient, grown in the laboratory, and returned after the patient's immune system has been weakened with immune-suppressing drugs. Some patients will also receive interleukin-2 (IL-2), a drug that may enhance the activity of the re-infused lymphocytes. Patients with metastatic melanoma (melanoma whose tumor has spread) who have been treated unsuccessfully with gp100 vaccination may participate in this study. They will undergo apheresis or a tumor biopsy, or both, to collect lymphocytes. In apheresis, whole blood is drawn through a needle in the arm. A machine separates the blood components and removes the white cells. The rest of the blood is returned to the donor through a needle in the other arm. A biopsy is a surgical procedure to remove a small piece of tumor tissue. Several weeks before the lymphocytes are collected, patients will receive injections of growth colony stimulating factor (G-CSF) every day for five days. This drug stimulates white cell production, permitting as many cells as possible to be obtained during collection. The lymphocytes will then be grown in larger numbers in the laboratory. Seven days before the cells are re-infused, the patient is admitted to the hospital and a catheter (small tube) is placed in a large vein in the chest or neck. Two drugs, cyclophosphamide and fludarabine, are given through the tube. These drugs suppress the immune system so that it will not interfere with the work of the reinfused lymphocytes. The lymphocytes are then injected through the catheter over a 30-minute period. After the infusion, patients who receive IL-2 will be given the drug in a high dose over a 15-minute period every eight hours for up to five days. Patients whose condition does not permit high-dose IL-2, such as those with a heart condition or lung problem, may receive a low-dose regimen, with the drug given as a shot under the skin of the thigh or abdomen for five days followed by a 2-day break, continuing for a total of six weeks. These patients receive a higher dose the first week and then half that dose the next five weeks. Blood and tissue samples will be taken before and during the study to evaluate the size of the tumor and assess treatment. If, 3-5 weeks after therapy is completed, the patient's tumor has stabilized or shrunk, the entire treatment, except for chemotherapy, may be repeated two more times.

Detailed description

Patients with metastatic melanoma who are human immunodeficiency virus (HIV) and Hepatitis B negative and who have previously progressed after receiving standard therapy will receive a nonmyeloablative but lymphocyte depleting preparative regimen consisting of cyclophosphamide and fludarabine and then will be treated by the adoptive transfer of lymphocytes reactive with shared antigens on their tumors. This study will evaluate the toxicity, immunologic effects and potential therapeutic role of this treatment.

Interventions

gp100 = gp100:209-217(210M) peptide - 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus gp100:209-217(210M) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections. MART-1 = MART-1:26-35(27L) peptide- 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus MART-1:26-35(27L) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections.

MART-1 = MART-1:26-35(27L) peptide- 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus MART-1:26-35(27L) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections.

DRUGIL-2

125,000 IU/kg dose intravenous for 5 days for 6 weeks with 2 days rest per week. 720,000 IU/kg intravenous every 8 hours for a maximum of 12 doses.

DRUGMART-1:26-35(27L)

MART-1 = MART-1:26-35(27L) peptide- 1 mg in IFA SQ (in the subcutaneous tissue of each thigh) on the morning of the cell infusion, plus MART-1:26-35(27L) peptide, 1 mg, in IFA injected into the subcutaneous tissue in two equal volumes, 1.0 mL for each injection, within 2cm of each other, in the thigh daily for five days starting on the morning of the cell infusion and then weekly for 3 more injections.

BIOLOGICALAbl cells

Abl cells IV = Lymphocytes 10\^9-10\^11 IV over 30 minutes on day 0, repeated in 14 to 21 days Abl cells IA = Lymphocytes 10\^9-10\^11 IA over 30 minutes on day 0, repeated in 14 to 21 days

DRUGFludarabine

5x25 mg/m\^2 intravenous

DRUGCyclophosphamide

2x30 mg/kg, 2x60 mg/kg intravenous

BIOLOGICALGCSF (Growth colony stimulating factor)

Beginning on day 1 or 2, GCSF will be administered subcutaneously at a dose of 5mcg/kg/day (not to exceed 300 mcg/day. Filgrastim administration will continue daily until neutrophil count \> 1.0 x10\^9/L x 3 days or \> 5.0 x10\^9/L.

PROCEDUREApheresis

Sponsors

National Cancer Institute (NCI)
Lead SponsorNIH

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* INCLUSION CRITERIA * Patients must have evaluable metastatic melanoma that is refractory to standard therapy. * Age greater than or equal to 16 years. * Patients of both genders must be willing to practice birth control for four months after receiving the preparative regimen. * Clinical performance status of Eastern Cooperative Oncology Group (ECOG) 0, 1 at entry to the trial and at the time of chemotherapy induction. * Absolute neutrophil count greater than 1000/mm\^3. * Platelet count greater than 100,000/mm\^3. * Hemoglobin greater than 8.0 g/dl. * Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) less than two times the upper limit of normal. * Serum creatinine less than or equal to 1.6 mg/dl. * Total bilirubin less than or equal to 1.6 mg/dl, except for patients with Gilbert's Syndrome who must have a total bilirubin less than 3.0 mg/dl. * More than four weeks must have elapsed since any prior therapy at the time the patient receives the preparative regimen. * Women of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects of the preparative chemotherapy on the fetus. * Life expectancy of greater than three months. * No steroid therapy required. * Seronegative for human immunodeficiency virus (HIV) antibody. (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who are HIV seropositive can have decreased immune competence and thus be less responsive to the experimental treatment and more susceptible to its toxicities.) * Seronegative for hepatitis B antigen. * Patients to receive high dose interleukin 2 (IL-2) must have no active systemic infections, coagulation disorders or other major medical illnesses of the cardiovascular, respiratory or immune system. * Patients who will receive high dose IL-2 as part of the phase I portion of this study or who will be randomized must be eligible to receive high dose IL-2. * Any patient receiving IL-2 must sign a durable power of attorney.

Design outcomes

Primary

MeasureTime frameDescription
Clinical ResponseEvery three to four weeks after the treatment, for up to 5 years.Complete response (CR) is defined as the disappearance of all clinical evidence of disease. Partial response (PR) is a 50% or greater decrease in the sum of the products of perpendicular diameters of all measurable lesions for at least one month. No new lesions may appear, and none may increase. Minor response (MR) is a 25-49% decrease in the sum of the products of the perpendicular diameters of all measurable lesions. Appearance of new lesions following a PR or CR are considered relapses. Patients with progressive disease (PD) and no evidence of stable disease will be taken off study after receiving IL-2.

Secondary

MeasureTime frameDescription
Number of Participants With Adverse Events10.5 monthsHere is the number of participants with adverse events. For a detailed list of adverse events see the adverse event module.

Countries

United States

Participant flow

Participants by arm

ArmCount
Cells IV + Cyclophosphamide 30mg/kg
Phase 1 Cyclophosphamide Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x30mg/kg + Cells IV
3
Cells IV + Cyclophosphamide 60mg/kg
Phase 1 Cyclophosphamide Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV
3
Cells IV + Low-Dose IV IL-2 (Initial)
Phase 1 IL-2 Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (72,000 IU/kg q8h for a maximum of 15 doses)
3
Cells IV + High-Dose IV IL-2 (Initial)
Phase 1 IL-2 Dose Escalation: Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses)
6
Cells IV + MTD IL-2
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) + G-CSF (to shorten time to neutrophil recovery)
51
Cells IA + MTD IL-2 (Prior Cells IV on 6)
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IA + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) Prior Cells IV + G-CSF
4
Cells IA + MTD IL-2
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IA + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) + G-CSF
7
Cells IA + MTD IL-2 (MART-1 Reactive)
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IA + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) + G-CSF + MART-1:26-35(27L) Peptide 1mg/day (5-8 days) in patients with MART-1 reactive cells
8
Cells IV + MTD IL-2 no GCSF
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) without G-CSF (to determine if G-CSF has harmful effects when adoptively transferring lymphocytes following a nonmyeloablative chemotherapy regimen)
6
Cells IV + MTD IL-2 no GCSF (gp100 Reactive)
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) without G-CSF + gp100:209-217(210M) 1mg/day (2-8 days) in patients with gp100 reactive cells
1
Cells IV + MTD IL-2 no GCSF (MART-1 Reactive)
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + IV IL-2 (720,000 IU/kg q8h for a maximum of 12 doses) without G-CSF + MART-1:26-35(27L) Peptide 1mg/day (5-8 days) in patients with MART-1 reactive cells
7
Cells IV + SQ IL-2 w/GCSF
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + SQ IL-2 (125,000 IU/kg/dose for 5 days for six weeks with 2 days rest per week) + G-CSF (to shorten time to neutrophil recovery), reactivity not specified
6
Cells IV + SQ IL-2 w/GCSF (MART-1 Reactive)
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + SQ IL-2 (125,000 IU/kg/dose for 5 days for six weeks with 2 days rest per week) + G-CSF + MART-1:26-35(27L) Peptide 1mg/day (5-8 days) in patients with MART-1 reactive cells
3
Cells IV + SQ IL-2 w/GCSF (no Reactivity)
Phase 2 Fludarabine 5x25mg/m2 + Cyclophosphamide 2x60mg/kg + Cells IV + SQ IL-2 (125,000 IU/kg/dose for 5 days for six weeks with 2 days rest per week) + G-CSF in patients with no reactivity
2
Total110

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003FG004FG005FG006FG007FG008FG009FG010FG011FG012FG013FG014
Apheresis Periodnot able to manufacture treatment cells6000000000000000
Treatment PeriodDeath during treatment000001000000000
Treatment PeriodNot treated000000010000000

Baseline characteristics

CharacteristicCells IV + Cyclophosphamide 60mg/kgCells IV + Low-Dose IV IL-2 (Initial)Cells IV + High-Dose IV IL-2 (Initial)Cells IV + MTD IL-2Cells IA + MTD IL-2 (Prior Cells IV on 6)Cells IA + MTD IL-2Cells IA + MTD IL-2 (MART-1 Reactive)Cells IV + MTD IL-2 no GCSFCells IV + MTD IL-2 no GCSF (gp100 Reactive)Cells IV + MTD IL-2 no GCSF (MART-1 Reactive)Cells IV + SQ IL-2 w/GCSFCells IV + Cyclophosphamide 30mg/kgCells IV + SQ IL-2 w/GCSF (MART-1 Reactive)Cells IV + SQ IL-2 w/GCSF (no Reactivity)Total
Age, Categorical
<=18 years
0 Participants0 Participants1 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants1 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants1 Participants1 Participants
Age, Categorical
Between 18 and 65 years
3 Participants3 Participants5 Participants51 Participants4 Participants7 Participants8 Participants6 Participants1 Participants7 Participants6 Participants3 Participants3 Participants1 Participants108 Participants
Age Continuous52.3 years
STANDARD_DEVIATION 4.5
42.3 years
STANDARD_DEVIATION 13.3
37.8 years
STANDARD_DEVIATION 14.7
41.9 years
STANDARD_DEVIATION 12.7
38.0 years
STANDARD_DEVIATION 14.3
39.7 years
STANDARD_DEVIATION 11.1
41.8 years
STANDARD_DEVIATION 11.6
49.0 years
STANDARD_DEVIATION 10.3
62.0 years40.7 years
STANDARD_DEVIATION 9.9
44.2 years
STANDARD_DEVIATION 11.2
41.3 years
STANDARD_DEVIATION 9.3
37.7 years
STANDARD_DEVIATION 7.1
58.5 years
STANDARD_DEVIATION 10.6
45.0 years
STANDARD_DEVIATION 11.4
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants3 Participants0 Participants0 Participants0 Participants0 Participants0 Participants1 Participants0 Participants0 Participants0 Participants0 Participants4 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
3 Participants3 Participants6 Participants48 Participants4 Participants7 Participants8 Participants6 Participants1 Participants6 Participants6 Participants3 Participants3 Participants2 Participants106 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants1 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants1 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
3 Participants3 Participants6 Participants50 Participants4 Participants7 Participants8 Participants6 Participants1 Participants7 Participants6 Participants3 Participants3 Participants2 Participants109 Participants
Region of Enrollment
United States
3 participants3 participants6 participants51 participants4 participants7 participants8 participants6 participants1 participants7 participants6 participants3 participants3 participants2 participants110 participants
Sex: Female, Male
Female
1 Participants1 Participants2 Participants22 Participants0 Participants2 Participants5 Participants1 Participants1 Participants1 Participants1 Participants1 Participants0 Participants0 Participants38 Participants
Sex: Female, Male
Male
2 Participants2 Participants4 Participants29 Participants4 Participants5 Participants3 Participants5 Participants0 Participants6 Participants5 Participants2 Participants3 Participants2 Participants72 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
EG004
affected / at risk
EG005
affected / at risk
EG006
affected / at risk
EG007
affected / at risk
EG008
affected / at risk
EG009
affected / at risk
EG010
affected / at risk
EG011
affected / at risk
EG012
affected / at risk
EG013
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —— / —— / —— / —— / —— / —— / —— / —— / —— / —— / —— / —
other
Total, other adverse events
3 / 33 / 33 / 36 / 650 / 514 / 47 / 78 / 86 / 61 / 17 / 76 / 63 / 32 / 2
serious
Total, serious adverse events
0 / 30 / 30 / 30 / 69 / 510 / 42 / 71 / 80 / 60 / 10 / 70 / 61 / 31 / 2

Outcome results

Primary

Clinical Response

Complete response (CR) is defined as the disappearance of all clinical evidence of disease. Partial response (PR) is a 50% or greater decrease in the sum of the products of perpendicular diameters of all measurable lesions for at least one month. No new lesions may appear, and none may increase. Minor response (MR) is a 25-49% decrease in the sum of the products of the perpendicular diameters of all measurable lesions. Appearance of new lesions following a PR or CR are considered relapses. Patients with progressive disease (PD) and no evidence of stable disease will be taken off study after receiving IL-2.

Time frame: Every three to four weeks after the treatment, for up to 5 years.

ArmMeasureGroupValue (NUMBER)
Abl Cells IV + Cyclophosphamide 30 mg/kgClinical ResponseMixed Response0 Participants
Abl Cells IV + Cyclophosphamide 30 mg/kgClinical ResponsePartial Response0 Participants
Abl Cells IV + Cyclophosphamide 30 mg/kgClinical ResponseNo Response3 Participants
Abl Cells IV + Cyclophosphamide 30 mg/kgClinical ResponseStable Disease0 Participants
Abl Cells IV + Cyclophosphamide 30 mg/kgClinical ResponseProgressive Disease0 Participants
Abl Cells IV + Cyclophosphamide 30 mg/kgClinical ResponseComplete Response0 Participants
Abl Cells IV + Cyclophosphamide 30 mg/kgClinical ResponseMinor Response0 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgClinical ResponseMixed Response0 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgClinical ResponseStable Disease0 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgClinical ResponseComplete Response0 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgClinical ResponseNo Response3 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgClinical ResponseMinor Response0 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgClinical ResponseProgressive Disease0 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgClinical ResponsePartial Response0 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Clinical ResponseStable Disease0 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Clinical ResponseNo Response3 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Clinical ResponseComplete Response0 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Clinical ResponseProgressive Disease0 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Clinical ResponseMixed Response0 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Clinical ResponsePartial Response0 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Clinical ResponseMinor Response0 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Clinical ResponsePartial Response0 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Clinical ResponseStable Disease0 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Clinical ResponseMixed Response0 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Clinical ResponseMinor Response0 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Clinical ResponseComplete Response0 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Clinical ResponseNo Response6 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Clinical ResponseProgressive Disease0 Participants
Abl Cells IV + MTD IL-2Clinical ResponseProgressive Disease0 Participants
Abl Cells IV + MTD IL-2Clinical ResponseComplete Response3 Participants
Abl Cells IV + MTD IL-2Clinical ResponseStable Disease1 Participants
Abl Cells IV + MTD IL-2Clinical ResponsePartial Response14 Participants
Abl Cells IV + MTD IL-2Clinical ResponseNo Response32 Participants
Abl Cells IV + MTD IL-2Clinical ResponseMinor Response0 Participants
Abl Cells IV + MTD IL-2Clinical ResponseMixed Response0 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Clinical ResponseStable Disease0 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Clinical ResponseMinor Response0 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Clinical ResponseMixed Response0 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Clinical ResponseProgressive Disease0 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Clinical ResponsePartial Response0 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Clinical ResponseComplete Response0 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Clinical ResponseNo Response4 Participants
Abl Cells IA + MTD IL-2Clinical ResponsePartial Response0 Participants
Abl Cells IA + MTD IL-2Clinical ResponseProgressive Disease0 Participants
Abl Cells IA + MTD IL-2Clinical ResponseNo Response5 Participants
Abl Cells IA + MTD IL-2Clinical ResponseMinor Response0 Participants
Abl Cells IA + MTD IL-2Clinical ResponseMixed Response0 Participants
Abl Cells IA + MTD IL-2Clinical ResponseStable Disease0 Participants
Abl Cells IA + MTD IL-2Clinical ResponseComplete Response1 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Clinical ResponseMinor Response0 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Clinical ResponseStable Disease0 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Clinical ResponseComplete Response1 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Clinical ResponsePartial Response1 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Clinical ResponseProgressive Disease0 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Clinical ResponseMixed Response1 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Clinical ResponseNo Response5 Participants
Abl Cells IV + MTD IL-2 no GCSFClinical ResponsePartial Response1 Participants
Abl Cells IV + MTD IL-2 no GCSFClinical ResponseNo Response4 Participants
Abl Cells IV + MTD IL-2 no GCSFClinical ResponseMinor Response0 Participants
Abl Cells IV + MTD IL-2 no GCSFClinical ResponseMixed Response0 Participants
Abl Cells IV + MTD IL-2 no GCSFClinical ResponseStable Disease0 Participants
Abl Cells IV + MTD IL-2 no GCSFClinical ResponseComplete Response1 Participants
Abl Cells IV + MTD IL-2 no GCSFClinical ResponseProgressive Disease0 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Clinical ResponsePartial Response0 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Clinical ResponseMinor Response1 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Clinical ResponseNo Response0 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Clinical ResponseMixed Response0 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Clinical ResponseComplete Response0 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Clinical ResponseStable Disease0 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Clinical ResponseProgressive Disease0 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Clinical ResponseProgressive Disease0 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Clinical ResponseComplete Response0 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Clinical ResponseMixed Response0 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Clinical ResponseNo Response5 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Clinical ResponsePartial Response2 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Clinical ResponseStable Disease0 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Clinical ResponseMinor Response0 Participants
Abl Cells IV + SQ IL-2 With GCSFClinical ResponseProgressive Disease0 Participants
Abl Cells IV + SQ IL-2 With GCSFClinical ResponseMinor Response0 Participants
Abl Cells IV + SQ IL-2 With GCSFClinical ResponseMixed Response0 Participants
Abl Cells IV + SQ IL-2 With GCSFClinical ResponsePartial Response3 Participants
Abl Cells IV + SQ IL-2 With GCSFClinical ResponseNo Response3 Participants
Abl Cells IV + SQ IL-2 With GCSFClinical ResponseComplete Response0 Participants
Abl Cells IV + SQ IL-2 With GCSFClinical ResponseStable Disease0 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Clinical ResponseProgressive Disease0 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Clinical ResponseComplete Response0 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Clinical ResponsePartial Response1 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Clinical ResponseMixed Response0 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Clinical ResponseStable Disease0 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Clinical ResponseMinor Response0 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Clinical ResponseNo Response2 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Clinical ResponseMinor Response0 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Clinical ResponseNo Response2 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Clinical ResponseStable Disease0 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Clinical ResponseProgressive Disease0 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Clinical ResponseComplete Response0 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Clinical ResponsePartial Response0 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Clinical ResponseMixed Response0 Participants
Secondary

Number of Participants With Adverse Events

Here is the number of participants with adverse events. For a detailed list of adverse events see the adverse event module.

Time frame: 10.5 months

ArmMeasureValue (NUMBER)
Abl Cells IV + Cyclophosphamide 30 mg/kgNumber of Participants With Adverse Events3 Participants
Abl Cells IV + Cyclophosphamide 60 mg/kgNumber of Participants With Adverse Events3 Participants
Abl Cells IV+Low Dose IV IL-2 (Initial)Number of Participants With Adverse Events3 Participants
Abl Cells IV+High Dose IV IL-2 (Initial)Number of Participants With Adverse Events6 Participants
Abl Cells IV + MTD IL-2Number of Participants With Adverse Events50 Participants
Abl Cells IA + MTD (Prior Cells IV on 6)Number of Participants With Adverse Events4 Participants
Abl Cells IA + MTD IL-2Number of Participants With Adverse Events7 Participants
Abl Cells IA+MTD IL-2 (MART-1 Reactive)Number of Participants With Adverse Events8 Participants
Abl Cells IV + MTD IL-2 no GCSFNumber of Participants With Adverse Events6 Participants
Abl Cells IV+MTD IL-2 no GCSF(gp100 Reactive)Number of Participants With Adverse Events1 Participants
Abl Cells IV+MTD IL-2 no GCSF (MART-1reactive)Number of Participants With Adverse Events7 Participants
Abl Cells IV + SQ IL-2 With GCSFNumber of Participants With Adverse Events6 Participants
Abl Cells IV + SQ IL-2 With GCSF (MART-1 Reactive)Number of Participants With Adverse Events3 Participants
Abl Cells IV + SQ IL-2 With GCSF (no Reactivity)Number of Participants With Adverse Events2 Participants

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026