Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
Phase I Trial of MCARH109, a G Protein-Coupled Receptor Class C Group 5 Member D (GPRC5D)-Targeted Chimeric Antigen Receptor T-Cell Therapy for Multiple Myeloma: An Updated Analysis.
СтатьяКлиническое исследование I фазыПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Jurgens Eric M, Firestone Ross S, Chaudhari Jagrutiben, Hosszu Kinga, Devlin Sean M, Shah Urvi A, Landa Jonathan, McAvoy Devin P, Lesokhin Alexander M, Korde Neha, Hassoun Hani, Tan Carlyn R, Hultcrantz Malin, Shah Gunjan L, Landau Heather J, Chung David J, Scordo Michael, Eren Ozgur Can, Dogan Ahmet, Giralt Sergio A, Park Jae H, Rivière Isabelle, Brentjens Renier J, Smith Eric L, Wang Xiuyan, Usmani Saad Z, Mailankody Sham
Аннотация
MCARH109 is a first-in-class G protein-coupled receptor, class C, group 5, member D (GPRC5D)-targeted chimeric antigen receptor (CAR) T-cell therapy for patients with relapsed/refractory multiple myeloma. This phase I clinical trial included 17 patients and determined that MCARH109 is safe at a maximum tolerated dose of 150 × 106 CAR T cells. In this updated analysis, no new serious adverse events were reported at a median follow-up of 37 months. Overall, 12 (71%) of 17 patients responded, including seven (70%) of 10 patients previously treated with B-cell maturation antigen-targeted therapy. The median duration of response was 8.6 months (95% CI, 5.7 to not reached [NR]) with two patients sustaining a stringent complete response at the time of last follow-up, 32 months and 41 months, respectively. The median overall survival (OS) was NR and the 3-year OS estimate was 59% (95% CI, 40 to 88). Possible GPRC5D loss via immunohistochemistry was observed in 6 (60%) of 10 patients at relapse. High-dimensional spectral cytometry-based immune profiling associated an activated T-cell phenotype at apheresis with a response to MCARH109.