Stage II Bladder Urothelial Carcinoma AJCC v6 and v7, Stage III Bladder Urothelial Carcinoma AJCC v6 and v7, Stage IV Bladder Urothelial Carcinoma AJCC v7
Conditions
Brief summary
This phase II trial studies how well nivolumab works with radiation therapy in treating patients with urothelial bladder cancer that has spread from its original site of growth to nearby tissues or lymph nodes and are ineligible for chemotherapy. Monoclonal antibodies, such as nivolumab, may interfere with the ability of tumor cells to grow and spread. Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. Giving nivolumab and radiation therapy may work better in treating patients with urothelial bladder cancer.
Detailed description
PRIMARY OBJECTIVES: I. To compare the 12-month rate of progression-free survival (PFS) achieved with the combination of nivolumab, a programmed death (PD-1) inhibitor, and radiation therapy in localized/locally advanced urothelial cancer patients, who are chemotherapy ineligible, to a historical control reference 12-month PFS rate. SECONDARY OBJECTIVES: I. To assess the toxicity of concurrent nivolumab and radiation therapy in urothelial cancer. II. To determine overall response rate (ORR). III. To determine metastasis-free survival (MFS). IV. To determine overall survival (OS). V. To evaluate the quality of life and bladder functioning during and after the therapy. VI. To explore the relationships of PD-1 expression, PDL-1 expression, and the Th1/Th2 cytokine ratio to clinical outcomes (response, PFS, MFS, and OS). OUTLINE: Patients receive nivolumab intravenously (IV) over 30 minutes on day 1. Treatment repeats every 14 days (2 weeks) for up to 14 courses (6 months) in the absence of disease progression or unacceptable toxicity. Beginning 3 days of course 1, patients undergo radiation therapy over 32-35 on weeks 1, 3, 5, 7 and 9. After completion of study treatment, patients are followed up every 3 months for 12 months.
Interventions
DRUGNivolumab
Patients receive nivolumab IV over 30 minutes on day 1. Treatment repeats every 14 days (2 weeks) for up to 14 courses (6 months) in the absence of disease progression or unacceptable toxicity. Beginning 3 days of course 1, patients undergo radiation therapy over 32-35 on weeks 1, 3, 5, 7 and 9.
RADIATIONRadiation
Beginning 3 days of course 1, patients undergo radiation therapy over 32-35 on weeks 1, 3, 5, 7 and 9.
Sponsors
Bristol-Myers Squibb
Barbara Ann Karmanos Cancer Institute
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
\- Localized urothelial cancer of bladder with presence of transitional cell carcinoma (TCC) component; mixed histologies are allowed Clinical or pathologic stage T2 -T4 disease including T4a and 4b if feasible to treat with radiation therapy Locoregional lymph node metastases are permitted but patients with distant metastases are ineligible; imaging to evaluate for distant metastases should consist of a minimum of computed tomography (CT)/magnetic resonance imaging (MRI) of abdomen/pelvis or CT urogram and a chest x-ray (CXR) or CT chest; patients for which there is clinical suspicion or symptoms of bone metastasis should have a bone scan completed to rule out metastatic disease prior to enrollment on study Agreeable to consider radiation therapy (RT) for the urothelial cancer: patients have to be evaluated by a radiation oncologist and deemed to be candidates for RT The patients must not be candidates for chemotherapy due to at least one of the following reasons: * Performance status of 2 * Creatinine clearance =\< 60 ml/min as calculated by the Cockcroft-Gault formula * Cardiac disease such as New York Heart Association (NYHA) class III or IV heart failure or cardiac ischemia within the last 12 months, grade 2 or greater neuropathy, or other comorbidities based on which patient is not considered a candidate for chemotherapy Alkaline phosphatase =\< 3 x upper limit of normal Aspartate aminotransferase (AST) =\< 3 x upper limit of normal Alanine aminotransferase (ALT) =\< 3 x upper limit of normal Bilirubin \< 1.5 x upper limit of normal (ULN) Absolute neutrophil count \>= 1500/mm\^3 Hemoglobin \>= 9 g/dL Platelets \>= 100 K/mm\^3 Performance score (PS) of 0-2 by Zubrod score Life expectancy of 12 months Willingness to sign informed consent Patients cannot have active autoimmune disease or immunosuppressive conditions Serum creatinine =\< 1.5 X institutional ULN or creatinine clearance \> 40 ml/min as calculated by the Cockcroft-Gault formula In females with childbearing potential, or men with partners of child bearing potential, willingness to use adequate contraception for a minimum duration of 155 days in females and 215 days in males, after last dose of nivolumab Maximal tumor resection has been performed as feasible
Exclusion criteria
\- The subject has received cytotoxic chemotherapy (including investigational cytotoxic chemotherapy) or biologic agents (e.g., cytokines or antibodies) for urothelial cancer within 4 weeks, or intravesical Bacillus Calmette-Guerin (BCG) within 6 weeks of the first dose of study treatment Prior treatment with any PD-1 or PDL-1 inhibitor The subject has received therapeutic radiation: * To the bladder/prostate/rectum pelvis * To any other site(s) within 28 days of the first dose of study treatment Obstructive renal failure that is not relieved with stents or nephrostomy tube/s The subject has received any other type of investigational agent within 28 days before the first dose of study treatment Steroid doses greater than an equivalent of prednisone 10 mg daily The subject has prothrombin time (PT)/international normalized ratio (INR) or partial thromboplastin time (PTT) test results at screening \>= 2 x the laboratory ULN Uncontrolled hematuria The subject has uncontrolled, significant intercurrent or recent illness including, but not limited to, the following conditions: * Cardiovascular disorders such as uncontrolled arrhythmias or uncontrolled congestive heart failure * Gastrointestinal disorders particularly those associated with a high risk of perforation or fistula formation including: * Any of the following at the time of screening * Active peptic ulcer disease, * Active inflammatory bowel disease (including ulcerative colitis and Crohn's disease), diverticulitis, cholecystitis, symptomatic cholangitis or appendicitis * Any of the following within 6 months before the first dose of study treatment: * History of abdominal fistula * Bowel perforation The subject has a previously identified allergy or hypersensitivity to components of the study treatment formulation The subject is unable or unwilling to abide by the study protocol or cooperate fully with the investigator or designee Presence of another invasive malignancy, which required systemic therapy within 12 months of protocol enrollment, except for resected skin cancers or prostate cancer that is in remission Pregnant or nursing women Patient is a candidate for radical cystectomy as a potentially curative option. The patient may not be a candidate for radical cystectomy due to any of the following reasons: comorbidities, patient preference, or physician discretion. Patients with inherited syndromes associated with hypersensitivity to ionizing radiation (e.g., ataxia-telangiectasia, Nijmegen breakage syndrome)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free Survival (PFS) | From date of registration to date of first documented disease relapse/progression, or death from urothelial cancer whichever occurs first, assessed up to 12 months | PFS distribution will be summarized with the Kaplan-Meier (K-M) survivorship estimate. A graph of the K-M curve for PFS will be generated along with the Hall-Wellner 90% confidence band, and a display of the number of patients at risk at several time points, below the X-axis. Summary statistics (12-month PFS rate, median PFS, etc.) will be calculated from the K-M life table, each one with its respective 90% confidence interval (CI). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Metastasis-free Survival (MFS) | From registration to the appearance of metastases or cancer related death, assessed up to 12 months | MFS will be calculated as a rate at 1 year with a 90% confidence interval from the K-M life tables. |
| Overall Survival (OS) | From date of registration to death or last follow up, assessed up to 36 months | Summary statistics of OS will be calculated from the K-M life tables. K-M graphs of the censored OS distributions will also be generated. |
| Overall Response Rate (ORR) | Up to 12 months | ORR will be estimated among all patients. Frequency distributions of best response will be generated. The point estimate of the ORR will be computed, along with its 95% (Wilson type) CI. |
| PD-1 and PDL-1 Expression Analysis Using Immunohistochemistry (IHC) | Up to 12 months | PD-1 status will be checked on pre-therapy tumor tissue and will be correlated with the primary endpoint. Also, the PDL-1 status will be checked on pre-therapy tumor tissue and will be correlated with the primary endpoint. |
| Th1/Th2 Cytokine Ratio Analysis | Up to 12 months | The continuous markers (e.g., tumor infiltrating lymphocyte \[TIL\]s, Th1/Th2 cytokine ratio, etc.) will be summarized with standard descriptive statistics. These descriptive analyses of the serum markers will be performed for each time point at which the each marker is determined. Response (CR/PR vs not) will be modeled as a function of a dichotomized version of pre-study the continuous (ungrouped) markers (e.g., TILs from tissue, and the Th1/Th2 cytokine ratio from serum). The statistical goal of these exploratory analyses is to obtain the point and 95% CI estimates of the OR, and to simply determine the direction and approximate magnitude of these associations for use in planning a subsequent study. Censored PFS will be modeled as a function of a dichotomized version of the continuous (ungrouped) markers (e.g., TILs from tissue, and the Th1/Th2 cytokine ratio using Cox modelling strategy. |
| Quality of Life (QOL) and Bladder Functioning Questionnaires Assessment | Up to 12 months | The QOL score will be measured pre therapy, during therapy and after therapy to compare the changes. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Treatment (Nivolumab, Radiation Therapy) Given IV
Nivolumab: Patients receive nivolumab IV over 30 minutes on day 1. Treatment repeats every 14 days (2 weeks) for up to 14 courses (6 months) in the absence of disease progression or unacceptable toxicity. Beginning 3 days of course 1, patients undergo radiation therapy over 32-35 on weeks 1, 3, 5, 7 and 9.
Radiation: Beginning 3 days of course 1, patients undergo radiation therapy over 32-35 on weeks 1, 3, 5, 7 and 9. | 20 |
| Total | 20 |
Baseline characteristics
| Characteristic | Treatment (Nivolumab, Radiation Therapy) |
|---|---|
| Age, Continuous | 78.5 years |
| Pathological stage pT2b: Pathologically invades the outer half of the muscularis propria. | 2 Participants |
| Pathological stage pT2N1: Pathologically invades muscularis propria with a single node in the true pelvis | 1 Participants |
| Pathological stage pT2Nx: Pathologically tumor invades muscularis propria, Cancer in lymph nodes not measurable. | 6 Participants |
| Pathological stage pT2: Pathologically invades muscularis propria | 3 Participants |
| Pathological stage pT4: Pathologically directly invades into adjacent structures. | 2 Participants |
| Pathological stage T2Nx: Clinically main tumor invades muscularis propria, Cancer in lymph nodes cannot be measured. | 6 Participants |
| Performance Status 0 | 3 Participants |
| Performance Status 1 | 16 Participants |
| Performance Status 2 | 1 Participants |
| Prior Bacillus Calmette-Guerin (BCG) Therapy No | 15 Participants |
| Prior Bacillus Calmette-Guerin (BCG) Therapy Yes | 5 Participants |
| Prior Chemotherapy No | 17 Participants |
| Prior Chemotherapy Yes | 3 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants |
| Race (NIH/OMB) Black or African American | 4 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 16 Participants |
| Region of Enrollment United States | 20 participants |
| Sex: Female, Male Female | 5 Participants |
| Sex: Female, Male Male | 15 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 13 / 20 |
| other Total, other adverse events | 19 / 20 |
| serious Total, serious adverse events | 11 / 20 |
Outcome results
Primary
Progression-free Survival (PFS)
PFS distribution will be summarized with the Kaplan-Meier (K-M) survivorship estimate. A graph of the K-M curve for PFS will be generated along with the Hall-Wellner 90% confidence band, and a display of the number of patients at risk at several time points, below the X-axis. Summary statistics (12-month PFS rate, median PFS, etc.) will be calculated from the K-M life table, each one with its respective 90% confidence interval (CI).
Time frame: From date of registration to date of first documented disease relapse/progression, or death from urothelial cancer whichever occurs first, assessed up to 12 months
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Treatment (Nivolumab, Radiation Therapy) | Progression-free Survival (PFS) | 11.4 months |
Secondary
Metastasis-free Survival (MFS)
MFS will be calculated as a rate at 1 year with a 90% confidence interval from the K-M life tables.
Time frame: From registration to the appearance of metastases or cancer related death, assessed up to 12 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Treatment (Nivolumab, Radiation Therapy) | Metastasis-free Survival (MFS) | 63 % of patients metastases-free at 1 year |
Secondary
Overall Response Rate (ORR)
ORR will be estimated among all patients. Frequency distributions of best response will be generated. The point estimate of the ORR will be computed, along with its 95% (Wilson type) CI.
Time frame: Up to 12 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Treatment (Nivolumab, Radiation Therapy) | Overall Response Rate (ORR) | 65.0 percentage of response at 12 months |
Secondary
Overall Survival (OS)
Summary statistics of OS will be calculated from the K-M life tables. K-M graphs of the censored OS distributions will also be generated.
Time frame: From date of registration to death or last follow up, assessed up to 36 months
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Treatment (Nivolumab, Radiation Therapy) | Overall Survival (OS) | 15.6 months |
Secondary
PD-1 and PDL-1 Expression Analysis Using Immunohistochemistry (IHC)
PD-1 status will be checked on pre-therapy tumor tissue and will be correlated with the primary endpoint. Also, the PDL-1 status will be checked on pre-therapy tumor tissue and will be correlated with the primary endpoint.
Time frame: Up to 12 months
Population: Those patients that had pre-therapy tumor tissue analyzed for PD-1 and PD-L1 (18 participants total).
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Treatment (Nivolumab, Radiation Therapy) | PD-1 and PDL-1 Expression Analysis Using Immunohistochemistry (IHC) | PD-1 <5 | 44 % of patients progression-free at 1 year |
| Treatment (Nivolumab, Radiation Therapy) | PD-1 and PDL-1 Expression Analysis Using Immunohistochemistry (IHC) | PD-1 =>5 | 35 % of patients progression-free at 1 year |
| Treatment (Nivolumab, Radiation Therapy) | PD-1 and PDL-1 Expression Analysis Using Immunohistochemistry (IHC) | PD-L1 <5 | 36 % of patients progression-free at 1 year |
| Treatment (Nivolumab, Radiation Therapy) | PD-1 and PDL-1 Expression Analysis Using Immunohistochemistry (IHC) | PD-L1 =>5 | 55 % of patients progression-free at 1 year |
Secondary
Quality of Life (QOL) and Bladder Functioning Questionnaires Assessment
The QOL score will be measured pre therapy, during therapy and after therapy to compare the changes.
Time frame: Up to 12 months
Population: Measure not taken
Secondary
Th1/Th2 Cytokine Ratio Analysis
The continuous markers (e.g., tumor infiltrating lymphocyte \[TIL\]s, Th1/Th2 cytokine ratio, etc.) will be summarized with standard descriptive statistics. These descriptive analyses of the serum markers will be performed for each time point at which the each marker is determined. Response (CR/PR vs not) will be modeled as a function of a dichotomized version of pre-study the continuous (ungrouped) markers (e.g., TILs from tissue, and the Th1/Th2 cytokine ratio from serum). The statistical goal of these exploratory analyses is to obtain the point and 95% CI estimates of the OR, and to simply determine the direction and approximate magnitude of these associations for use in planning a subsequent study. Censored PFS will be modeled as a function of a dichotomized version of the continuous (ungrouped) markers (e.g., TILs from tissue, and the Th1/Th2 cytokine ratio using Cox modelling strategy.
Time frame: Up to 12 months
Population: Measure not taken