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PSCA-CAR T cell therapy in metastatic castration-resistant prostate cancer: a phase 1 trial

  • Tanya B. Dorff,
  • M. Suzette Blanchard,
  • Lauren N. Adkins,
  • Laura Luebbert,
  • Neena Leggett,
  • Stephanie N. Shishido,
  • Alan Macias,
  • Marissa M. Del Real,
  • Gaurav Dhapola,
  • Colt Egelston,
  • John P. Murad,
  • Reginaldo Rosa,
  • Jinny Paul,
  • Ammar Chaudhry,
  • Hripsime Martirosyan,
  • Ethan Gerdts,
  • Jamie R. Wagner,
  • Tracey Stiller,
  • Dileshni Tilakawardane,
  • Sumanta Pal,
  • Catalina Martinez,
  • Robert E. Reiter,
  • Lihua E. Budde,
  • Massimo D’Apuzzo,
  • Peter Kuhn,
  • Lior Pachter,
  • Stephen J. Forman,
  • Saul J. Priceman

摘要

Despite recent therapeutic advances, metastatic castration-resistant prostate cancer (mCRPC) remains lethal. Chimeric antigen receptor (CAR) T cell therapies have demonstrated durable remissions in hematological malignancies. We report results from a phase 1, first-in-human study of prostate stem cell antigen (PSCA)-directed CAR T cells in men with mCRPC. The starting dose level (DL) was 100 million (M) CAR T cells without lymphodepletion (LD), followed by incorporation of LD. The primary end points were safety and dose-limiting toxicities (DLTs). No DLTs were observed at DL1, with a DLT of grade 3 cystitis encountered at DL2, resulting in addition of a new cohort using a reduced LD regimen + 100 M CAR T cells (DL3). No DLTs were observed in DL3. Cytokine release syndrome of grade 1 or 2 occurred in 5 of 14 treated patients. Prostate-specific antigen declines (>30%) occurred in 4 of 14 patients, as well as radiographic improvements. Dynamic changes indicating activation of peripheral blood endogenous and CAR T cell subsets, TCR repertoire diversity and changes in the tumor immune microenvironment were observed in a subset of patients. Limited persistence of CAR T cells was observed beyond 28 days post-infusion. These results support future clinical studies to optimize dosing and combination strategies to improve durable therapeutic outcomes. ClinicalTrials.gov identifier NCT03873805.