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

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Washington

About this trial

This phase I/II 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 criteria

Qualifiers

Age >= 18 at the time of screening

Ability to understand and willingness to sign a written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of potential study participants

Histopathologically confirmed cTxN1-3M0, cTxNxM1 or cT4bNxM0 muscle invasive bladder cancer at initial diagnosis

Achieved a radiographic complete response (CR) or partial response (PR), per Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1 criteria and at the determination of treating physicians) after 3-9 cycles of induction EV + pembro

Disqualifiers

Prior radiation therapy with field overlapping with current proposed radiation field, precluding delivery of meaningful dose of radiation

Intracranial metastasis

Any small cell component, or predominant (> 50%) sarcomatoid or plasmacytoid histology

Other active malignancy or clinically relevant malignancy within past 2 years, per discussion with the principal investigator

Trial design

Treatments tested in this trial

  • Intensity-Modulated Radiation Therapy
  • Volume Modulated Arc Therapy
  • Cisplatin
  • Gemcitabine
  • Fluorouracil
  • Mitomycin
  • Radical Cystectomy
  • Pelvic Lymphadenectomy
  • Stereotactic Body Radiation Therapy
  • Computed Tomography
  • Positron Emission Tomography
  • Magnetic Resonance Imaging
  • Transurethral Resection of Bladder Tumor
  • Cystoscopy
  • Biospecimen Collection
  • Questionnaire Administration

Treatment groups

12 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Washington

Lead sponsor

Lopker Family Foundation

Collaborator