Enfortumab Vedotin and Pembrolizumab With Cystectomy and/or Ureterectomy for Locally Advanced or Metastatic Bladder and Upper Urothelial Tract Cancer, CAST-AI Trial

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

This phase IV trial tests the impact of standard of care enfortumab vedotin and pembrolizumab followed by removal of all or part of the bladder (cytoreductive cystectomy) and/or removal of all or part of the tube that carriers urine from the kidneys to the bladder (ureterectomy) on outcomes in patients with bladder and upper urothelial tract that has spread to nearby tissue or lymph nodes (locally advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). 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 tumor cells. Enfortumab attaches to a protein called nectin-4 on tumor 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 tumor and may interfere with the ability of tumor cells to grow and spread. Giving standard of care enfortumab vedotin and pembrolizumab followed by cytoreductive cystectomy and/or ureterectomy (CC/U) may improve outcomes in patients with locally advanced or metastatic bladder or upper urothelial tract cancer.

Eligibility criteria

Qualifiers

18 years of age or older at the time of informed consent

Histologically proven urothelial carcinoma [American Joint Committee on Cancer (AJCC) 2017] of the bladder (BCa) or upper urothelial tract (UTUC), N+ and/or M+. Initial diagnosis must be within 90 days of planned date for treatment initiation

The following variant histologic subtypes are permitted in any amount

Urothelial with squamous differentiation

Disqualifiers

Presence of urothelial carcinoma with histologic variants comprising > 50% of histology

Any amount: neuroendocrine, micropapillary, or signet ring cell features

Prior systemic chemotherapy for urothelial cell carcinoma of the bladder at any time (excluding intravesicular therapies)

Skin cancer (non-melanoma or melanoma) that is considered completely cured

Trial design

Treatments tested in this trial

  • Biospecimen Collection
  • Computed Tomography
  • Cystectomy
  • Enfortumab Vedotin
  • Local Therapy
  • Magnetic Resonance Imaging
  • Pembrolizumab
  • Positron Emission Tomography
  • Questionnaire Administration
  • Ureterectomy

Treatment groups

75 Participants
are divided into 1 treatment group

Sponsors and collaborators