Back to Search Start Over

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

Authors :
Dorff TB
Blanchard MS
Adkins LN
Luebbert L
Leggett N
Shishido SN
Macias A
Del Real MM
Dhapola G
Egelston C
Murad JP
Rosa R
Paul J
Chaudhry A
Martirosyan H
Gerdts E
Wagner JR
Stiller T
Tilakawardane D
Pal S
Martinez C
Reiter RE
Budde LE
D'Apuzzo M
Kuhn P
Pachter L
Forman SJ
Priceman SJ
Source :
Nature medicine [Nat Med] 2024 Jun; Vol. 30 (6), pp. 1636-1644. Date of Electronic Publication: 2024 Jun 12.
Publication Year :
2024

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 .<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1546-170X
Volume :
30
Issue :
6
Database :
MEDLINE
Journal :
Nature medicine
Publication Type :
Academic Journal
Accession number :
38867077
Full Text :
https://doi.org/10.1038/s41591-024-02979-8