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

Tanya B. Dorff(City Of Hope National Medical Center), M. Suzette Blanchard(City of Hope), Lauren Adkins(City of Hope), Laura Luebbert(California Institute of Technology), Neena A. Leggett(City of Hope), Stephanie N. Shishido(University of Southern California), Alan Macias(City of Hope), Marissa Morales Del Real(City of Hope), Gaurav Dhapola(City of Hope), Colt A. Egelston(City of Hope), John P. Murad(City of Hope), Reginaldo Cruz Alves Rosa(City of Hope), Jinny Paul(City of Hope), Ammar Chaudhry(City of Hope), Hripsime Martirosyan(City of Hope), Ethan Gerdts(City of Hope), Jamie R. Wagner(City of Hope), Tracey Stiller(City of Hope), Dileshni Tilakawardane(City of Hope), Sumanta K. Pal(City of Hope), Catalina Martínez(City of Hope), Robert E. Reiter(University of California, Los Angeles), Lihua E. Budde(City of Hope), Massimo D’Apuzzo(City of Hope), Peter Kühn(University of Southern California), Lior Pachter(California Institute of Technology), Stephen J. Forman(City of Hope), Saul J. Priceman(City Of Hope National Medical Center)
Nature Medicine
June 1, 2024
Cited by 113Open Access
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Abstract

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 .


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