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.

IF 42.1 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-02-10 Epub Date: 2024-12-04 DOI:10.1200/JCO-24-01785
Eric M Jurgens, Ross S Firestone, Jagrutiben Chaudhari, Kinga Hosszu, Sean M Devlin, Urvi A Shah, Jonathan Landa, Devin P McAvoy, Alexander M Lesokhin, Neha Korde, Hani Hassoun, Carlyn R Tan, Malin Hultcrantz, Gunjan L Shah, Heather J Landau, David J Chung, Michael Scordo, Ozgur Can Eren, Ahmet Dogan, Sergio A Giralt, Jae H Park, Isabelle Rivière, Renier J Brentjens, Eric L Smith, Xiuyan Wang, Saad Z Usmani, Sham Mailankody
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引用次数: 0

Abstract

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.

MCARH109,一种G蛋白偶联受体C类5成员D (GPRC5D)靶向嵌合抗原受体t细胞治疗多发性骨髓瘤的I期试验:最新分析
MCARH109是一类首个G蛋白偶联受体,C类,5组,成员D (GPRC5D)靶向嵌合抗原受体(CAR) t细胞治疗复发/难治性多发性骨髓瘤患者。这项I期临床试验包括17名患者,并确定MCARH109在150 × 106 CAR - T细胞的最大耐受剂量下是安全的。在这项最新的分析中,在中位随访37个月期间没有报告新的严重不良事件。总体而言,17例患者中有12例(71%)有应答,包括10例患者中有7例(70%)先前接受过b细胞成熟抗原靶向治疗。中位缓解持续时间为8.6个月(95% CI, 5.7至未达到[NR]),其中2例患者在最后一次随访时分别维持严格的完全缓解,分别为32个月和41个月。中位总生存期(OS)为NR, 3年OS估计为59% (95% CI, 40至88)。10例复发患者中有6例(60%)通过免疫组化观察到GPRC5D可能丢失。基于高维光谱细胞术的免疫分析将分离时活化的t细胞表型与对MCARH109的反应联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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