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PSCA-CAR T cell therapy in metastatic castration-resistant prostate cancer: a phase 1 trial.
- 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).)
- Subjects :
- Humans
Male
Aged
Middle Aged
Receptors, Chimeric Antigen immunology
Neoplasm Metastasis
T-Lymphocytes immunology
T-Lymphocytes transplantation
Prostate-Specific Antigen blood
Prostatic Neoplasms, Castration-Resistant therapy
Prostatic Neoplasms, Castration-Resistant immunology
Prostatic Neoplasms, Castration-Resistant pathology
Antigens, Neoplasm immunology
Immunotherapy, Adoptive adverse effects
Immunotherapy, Adoptive methods
GPI-Linked Proteins immunology
Neoplasm Proteins immunology
Subjects
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