Bladder Preservation for Patients With Muscle Invasive Bladder Cancer (MIBC) With Variant Histology

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorLeslie Ballas

About this trial

This is a Phase II, single cohort study designed to evaluate outcomes in patients with muscle invasive bladder cancer (MIBC) with variant histology who receive neoadjuvant chemotherapy (NAC) with or without immunotherapy (IO) followed by trimodal therapy (TMT). Enrolled patients will undergo at least 3 cycles of NAC +/- IO (oncologist's choice) followed by a four- or six-week course of concurrent standard of care chemotherapy and radiation therapy. These patients will be compared with historical controls of patients with a diagnosis of pure urothelial carcinoma who have undergone TMT. This study has been designed to test the hypothesis that variant histology TMT can be delivered within 45 days of NAC +/- IO and is therefore a viable option in patients who are risk of systemic disease spread.

Eligibility criteria

Qualifiers

Documented diagnosis of MIBC with variant histology, cT2-T4N0M0, confirmed by TURBT and CT C/A/P and/or PET.

Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.

Disqualifiers

Evidence of diffuse cis on pathology

Presence of bilateral hydronephrosis (if hydronephrosis is present, can only be unilateral)

Prior radiotherapy to the pelvis

History of systemic therapy for MIBS

Trial design

Treatments tested in this trial

  • Trimodal therapy (TMT) within 45 days of neoadjuvant chemotherapy (NAC)

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators

Leslie Ballas

Lead sponsor

Cedars-Sinai Medical Center

Sponsor institution