RecruitingPhase 2NCT07087860

Therapeutic Plasma Exchange With Enfortumab Vedotin and Pembrolizumab for Treatment of Bladder Cancers

MC220503 Randomized Phase II Rescuing Cancer Immunotherapy With Plasma Exchange in Bladder Cancer 1 (ReCIPE-B1)


Sponsor

Mayo Clinic

Enrollment

70 participants

Start Date

Aug 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II trial compares therapeutic plasma exchange followed by enfortumab vedotin and pembrolizumab to standard of care next-line therapy for the treatment of patients with bladder or upper urinary tract cancers that have spread from where they first started (primary site) to other places in the body (metastatic) and that have not responded to previous treatment (refractory). TPE is a process that slowly removes a patient's blood through an intravenous or central line. The blood is sent through a machine that separates the plasma (the liquid part of blood) from other blood components (red cells, white cells, platelets). The plasma is then removed. The remaining blood components are combined with replacement fluid and returned to the patient's bloodstream through the intravenous or central line. Enfortumab vedotin is a monoclonal antibody, enfortumab, linked to an anticancer drug called vedotin. It works by helping the immune system to slow or stop the growth of cancer cells. Enfortumab attaches to a protein called nectin-4 on cancer cells in a targeted way and delivers vedotin to kill them. It is a type of antibody-drug conjugate. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Treatment with enfortumab vedotin and pembrolizumab is already approved by the Food and Drug Administration for the treatment of bladder cancer, but TPE is not. Combining TPE with enfortumab vedotin and pembrolizumab may work better than standard of care options for treating metastatic and refractory bladder and urinary tract cancers. This study also evaluates the effect of TPE with standard of care antibody drug conjugates (ADCs) in treating patients with refractory metastatic bladder cancer. ADC therapy is treatment with a monoclonal antibody linked to a chemotherapy drug. It is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of tumor cells, and delivers chemotherapy to kill them. Giving TPE with standard of care ADC therapy may be effective in treating patients with refractory metastatic bladder cancer.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether adding therapeutic plasma exchange (a procedure that filters and cleans the blood) to standard immunotherapy and chemotherapy improves outcomes for people with bladder cancer or upper urinary tract cancer, including those whose cancer has returned after prior treatment. **You may be eligible if...** - You are 18 or older - You have been diagnosed with urothelial carcinoma (bladder or upper urinary tract cancer) - Your cancer has progressed despite prior treatment with enfortumab vedotin and pembrolizumab (Group A/B), OR you are newly starting this treatment (Group C) - You have adequate organ function **You may NOT be eligible if...** - You have certain autoimmune conditions - You have uncontrolled infections or other serious medical conditions - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

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

OTHERBest Practice

Receive standard of care

PROCEDUREBiospecimen Collection

Undergo collection of blood and urine samples

PROCEDURECentral Venous Cannula Insertion

Undergo central line placement

PROCEDUREComputed Tomography

Undergo CT or PET/CT

DRUGEnfortumab Vedotin

Given IV

PROCEDUREMagnetic Resonance Imaging

Undergo MRI

BIOLOGICALPembrolizumab

Given IV

PROCEDUREPlasmapheresis

Undergo TPE

PROCEDUREPositron Emission Tomography

Undergo PET/CT

OTHERQuestionnaire Administration

Ancillary studies

BIOLOGICALAntibody-Drug Conjugate Therapy

Given IV


Locations(1)

Mayo Clinic in Rochester

Rochester, Minnesota, United States

View Full Details on ClinicalTrials.gov

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NCT07087860


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