嵌合抗原受体
细胞因子释放综合征
医学
多发性骨髓瘤
抗原
抗体
免疫学
内科学
肿瘤科
免疫疗法
免疫系统
癌症研究
临床研究阶段
临床试验
细胞因子
汽车T细胞治疗
无进展生存期
沙利度胺
醛类白血病
存活率
生存分析
淋巴瘤
作者
Mengmeng Pan,Di Wang,Jie Xu,Shiwei Jin,Yan Wang,Tao Yi,Yuanfang Liu,Wanyan Ouyang,Xiangqin Weng,Hongmei Yi,Yu Huang,Xin‐Mei Cao,Shuhua Li,Fuyuan Zhang,Weiping Zhang,Chunrui Li,Jian‐Qing Mi
出处
期刊:Blood
[Elsevier BV]
日期:2025-10-21
卷期号:147 (5): 513-519
被引量:3
标识
DOI:10.1182/blood.2025030559
摘要
ABSTRACT: GPRC5D has emerged as a promising therapeutic target in relapsed/refractory multiple myeloma (R/R MM), particularly following progression after B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T-cell (CAR-T) therapies. RD118 is a novel CAR-T therapy incorporating a fully human single-domain antibody fragment targeting GPRC5D. In this phase 1 study, 18 R/R patients (17 with MM and 1 with a history of primary plasma cell leukemia) received a single infusion of RD118 at 1.0 × 106, 2.0 × 106, or 3.0 × 106 CAR+ T cells per kg. At a median follow-up of 17.0 months, the overall response rate (ORR) was 94.4%, including 72.2% complete or stringent complete responses. Among the 7 patients previously exposed to BCMA-directed CAR-T therapy, ORR reached 85.7%. Median progression-free survival (PFS) was 18.2 months (95% confidence interval, 14.4 to not estimable), with 12-month PFS and overall survival rates of 82.1% and 93.3%, respectively. Cytokine release syndrome occurred in 88.9% of the patients, primarily grade 1 to 2. One patient developed grade 3 immune effector cell-associated neurotoxicity, which resolved within 72 hours. No cerebellar toxicities or treatment-related deaths were reported. These findings support that RD118 is a highly effective and safe therapeutic option for heavily pretreated R/R MM. This trial was registered at www.clinicaltrials.gov as #NCT05759793 and #NCT05219721.
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