RecruitingPhase 1Phase 2NCT07579195

Consolidative Therapy After EV + Pembrolizumab in Muscle Invasive Bladder Cancer, REINFORCE Trial

Consolidative Radiation Therapy or Cystectomy After Initial Favorable Response Succeeding Enfortumab Vedotin Plus Pembrolizumab (REINFORCE)--- A Pilot Feasibility Trial


Sponsor

University of Washington

Enrollment

12 participants

Start Date

Aug 20, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This pilot feasibility clinical trial is evaluating a novel treatment strategy for patients with advanced bladder cancer that is unresectable, has spread to nearby lymph nodes or a limited number of distant sites (oligometastatic disease), and has responded to initial treatment with enfortumab vedotin and pembrolizumab. Although this combination has significantly improved outcomes compared to traditional chemotherapy, many patients are left with residual cancer in the bladder or other sites, and there is currently no established standard approach for managing this remaining disease or determining the optimal duration of systemic therapy. Prolonged treatment can lead to cumulative side effects and negatively impact quality of life. This study investigates whether adding consolidative treatment-such as radiation therapy to the bladder and metastatic sites or surgical removal of the bladder (radical cystectomy)-can safely eliminate residual disease and delay cancer progression. Radiation therapy uses high-energy x-rays to precisely target and destroy cancer cells while minimizing exposure to surrounding normal tissues. In selected patients, surgery may be used to remove remaining tumor in the bladder. Targeted radiation techniques, such as stereotactic body radiation therapy (SBRT), may also be used to treat small metastatic sites. This approach may allow for safe discontinuation of systemic therapy, potentially reducing long-term treatment-related side effects. A key component of this trial is the integration of biomarker testing using circulating tumor DNA (ctDNA) from blood and urine tumor DNA (utDNA). These tests detect small amounts of tumor-derived genetic material and may help identify patients most likely to benefit from consolidative treatment, as well as guide decisions about ongoing therapy. By combining response to systemic therapy with personalized local treatment and biomarker-driven monitoring, this study aims to improve cancer control, reduce complications from untreated local disease, and inform future treatment strategies for patients with advanced bladder cancer.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Biospecimen Collection, a procedure called Computed Tomography, and others for people with muscle-invasive bladder carcinoma, stage iii bladder cancer ajcc v8, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONIntensity-Modulated Radiation Therapy

Undergo IMRT

RADIATIONVolume Modulated Arc Therapy

Undergo VMAT

DRUGRadiosensitizing Agent

Given radiosensitizing chemotherapy

PROCEDURERadical Cystectomy

Undergo radical cystectomy

PROCEDUREPelvic Lymphadenectomy

Undergo pelvic lymph node dissection

RADIATIONStereotactic Body Radiation Therapy

Undergo SBRT

PROCEDUREComputed Tomography

Undergo CT and/or PET/CT

PROCEDUREPositron Emission Tomography

Undergo PET/CT

PROCEDUREMagnetic Resonance Imaging

Undergo MRI

PROCEDURETransurethral Resection of Bladder Tumor

Undergo re-TURBT

PROCEDURECystoscopy

Undergo cystoscopy

PROCEDUREBiospecimen Collection

Undergo collection of blood and urine samples

OTHERQuestionnaire Administration

Ancillary studies


Locations(1)

Fred Hutch/University of Washington Cancer Consortium

Seattle, Washington, United States

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NCT07579195


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