Recruiting
Phase 3
Enfortumab Vedotin in Combination With Pembrolizumab vs. Concurrent Chemoradiotherapy (cCRT) in People With Muscle Invasive Bladder Cancer (EV-309)
Condition(s) studied
Urothelial CancerUrinary Bladder Neoplasms
Investigational drug(s) / intervention(s)
Enfortumab vedotinConventional RadiotherapyHypofractionated RadiotherapyCisplatinFluorouracilMitomycin CGemcitabinePembrolizumab
Enfortumab vedotin: Enfortumab vedotin administered as an IV infusion on Days 1 and 8 of every 3-week cycle up to cycle 9.
Conventional Radiotherapy: 64 Gy in 32 fractions over 6.5 weeks administered to the participant's bladder only or the bladder and prophylactically to pelvic nodes.
Hypofractionated Radiotherapy: 55 Gy in 20 fractions over 4 weeks administered to the participant's bladder only.
Cisplatin: 40 mg of cisplatin per meter squared of body surface area, administered once weekly via IV infusion during radiation OR 20 mg of cisplatin per meter squared of body surface area per day on Days 1 and 2 weekly via IV infusion during radiation.
Fluorouracil: 500 mg per meter squared of body surface area per day on Days 1-5 (week 1) and Days 22 26 (week 3) administered as continuous IV infusion during radiation in combination with mitomycin C.
Mitomycin C: 12 mg per meter squared of body surface area administered as an IV bolus on Day 1 during radiation in combination with fluorouracil.
Gemcitabine: 100 mg per meter squared of body surface area administered once weekly via IV infusion during radiation OR 27 mg per meter squared of body surface area administered twice weekly via IV infusion during radiation
Pembrolizumab: IV infusion on Day 1 of every 3-week cycle up to cycle 17.
Study summary
This study is being done to see how well two drugs (enfortumab vedotin and pembrolizumab) work together as a bladder preservation approach to treat patients with muscle invasive bladder cancer. The study will compare these drugs to concurrent chemoradiotherapy that is usually used to treat this cancer (standard of care). The study will enroll patients with muscle-invasive bladder cancer (MIBC) who have cancer that has not spread outside the bladder.
Eligibility
Inclusion Criteria:
* Has histologically confirmed initial diagnosis of muscle-invasive bladder cancer (MIBC) with predominant urothelial histology staged cT2-T4aN0M0
* Tissue comprising muscle-invasive urothelial cancer must be submitted for clinical staging at baseline
* Eligible for and agree to receive chemoradiotherapy and one of the protocol-specified radiosensitizing chemotherapy regimens
* Fit for systemic therapy and elect bladder preservation, including participants who are ineligible for or have elected not to undergo cystectomy
* Has Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
Exclusion Criteria:
* Advanced or metastatic disease (N+, M1), non-urothelial carcinoma, diffuse or multifocal CIS, urothelial carcinoma or histological variant at any site outside the urinary bladder within previous 24 months prior to randomization except Ta/T1/CIS of the upper urinary tract including renal pelvis and ureter if the participant had undergone complete nephrectomy
* Has received any prior systemic treatment, chemoradiation, and/or radiation for MIBC or NMIBC
* Prior pelvic radiation for any reason
* Inadequate bladder function
* Other active malignancies within 3 years prior to randomization
* Previously treated with enfortumab vedotin or other MMAE-based antibody-drug conjugates (ADCs)
* Previously treated with a PD(L)-1 inhibitor, defined as a PD-1 inhibitor or PD-L1 inhibitor
* Uncontrolled diabetes
* Currently receiving systemic antimicrobial treatment for active infection (viral, bacterial, or fungal) at the time of randomization. Routine antimicrobial prophylaxis is permitted
* Known active hepatitis B, active hepatitis C, or human immunodeficiency virus (HIV) infection
* Received major surgery (defined as requiring general anesthesia and \>24 hour inpatient hospitalization) within 4 weeks prior to randomization
* Known severe (≥ Grade 3) hypersensitivity to any enfortumab vedotin excipient contained in the drug formulation of enfortumab vedotin
* Known genetic disorders associated with radiosensitivity (eg, ataxia telangiectasia, Nijmegen breakage syndrome, Fanconi syndrome)
* Active keratitis or corneal ulcerations
* History of autoimmune disease that has required systemic treatment in the past 2 years
* History of idiopathic pulmonary fibrosis, organizing pneumonia, drug induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest computed tomography (CT) scan
* Prior allogeneic stem cell or solid organ transplant
* Received a live attenuated vaccine within 30 days prior to randomization
Primary outcome measure(s)
- Bladder-intact Event Free Survival (BI-EFS) by Blinded Independent Central Review (BICR) — Up to approximately 45.5 months
BI-EFS is defined as the time from randomization to any of the following events: histologically confirmed persistent or residual MIBC post-treatment confirmed by BICR, histologically confirmed recurrent MIBC by BICR, disease progression by BICR, cystectomy, or death from any cause.
- Overall Survival (OS) — Up to approximately 60 months
Time from randomization to death due to any cause.
Trial sites (14)
| Facility | City | Region | Status |
| Samsun Clinic - Ridley-Tree Cancer Center |
Santa Barbara |
California |
Recruiting |
| Rocky Mountain Cancer Center |
Aurora |
Colorado |
Recruiting |
| Medical Oncology Hematology Consultants |
Newark |
Delaware |
Recruiting |
| Illinois Cancer Specialists |
Niles |
Illinois |
Recruiting |
| Fort Wayne Medical Oncology and Hematology |
Fort Wayne |
Indiana |
Recruiting |
| Missouri Cancer Associates |
Columbia |
Missouri |
Recruiting |
| Oncology Hematology Care Clinical Trials, LLC |
Fairfield |
Ohio |
Recruiting |
| Williamette Valley Cancer Institute and Research Center |
Eugene |
Oregon |
Recruiting |
| Compass Oncology - West |
Tigard |
Oregon |
Recruiting |
| SCRI Oncology Partners |
Nashville |
Tennessee |
Recruiting |
| Texas Oncology |
Austin |
Texas |
Recruiting |
| Texas Oncology - Northeast Texas |
Tyler |
Texas |
Recruiting |
| Virginia Oncology Associates |
Norfolk |
Virginia |
Recruiting |
| Site CA01071 |
Montreal |
Quebec |
Recruiting |