Robat-Jazi Behrouz, Mahalleh Mehrdad, Dashti Mohsen, Nejati Negar, Ahmadpour Mahsa, Alinejad Erfan, Mohammadi Shiva, Lorestani Parsa, Hamidieh Amir Ali, Habibi Mohammad Amin, Jadidi-Niaragh Farhad
Inflammation Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Anticancer Agents Med Chem. 2025;25(14):1017-1028. doi: 10.2174/0118715206350342241224073809.
Despite ongoing advances and introducing innovative therapeutic approaches for the treatment of multiple myeloma (MM), relapses are common, with low overall survival rates. G protein-coupled receptor, class C, group 5, and member D (GPRC5D) has been expressed in several myeloma cell lines and has demonstrated encouraging outcomes results in studies as a potential target for immunotherapies.
We aimed to investigate the safety and efficacy of GPRC5D-targeted CAR T cell therapies in MM patients.
On August 24, 2023, the databases of PubMed, Scopus, Embase, and Web of Science were systematically searched for pertinent studies. After completing a two-step title/abstract and full-text screening process, the eligible studies were included.
Following the screening of 107 articles, four studies of 130 multiple myeloma patients treated with GPRC5D-targeted CAR T-cell therapy were included. The meta-analyses showed an ORR of 87% (95% CI [81- 93%]), with 74% (95% CI [65-73%]) for those with prior BCMA-targeted therapy and 88% (95% CI [78-99%]) for those without. PR was 25%, VGPR 33%, and CR/sCR 48%, with 65% achieving MRD-negativity. In terms of safety, hematologic AEs were common, with anemia reported in 86% of patients. Non-hematologic common AEs included CRS (83%, 5% grade ≥3) and hypocalcemia (63%, 10% grade ≥3). No significant publication bias was detected.
GPRC5D is an active and safe target that shows promising results in the treatment of relapsed and/or refractory (R/R) MM and heavily pretreated patients.
尽管在多发性骨髓瘤(MM)的治疗方面不断取得进展并引入了创新的治疗方法,但复发仍然很常见,总体生存率较低。G蛋白偶联受体C类第5组成员D(GPRC5D)已在多种骨髓瘤细胞系中表达,并在研究中作为免疫治疗的潜在靶点显示出令人鼓舞的结果。
我们旨在研究靶向GPRC5D的嵌合抗原受体(CAR)T细胞疗法在MM患者中的安全性和疗效。
2023年8月24日,系统检索了PubMed、Scopus、Embase和Web of Science数据库中的相关研究。在完成两步标题/摘要和全文筛选过程后,纳入符合条件的研究。
在筛选的107篇文章中,纳入了4项关于130例接受靶向GPRC5D的CAR T细胞疗法治疗的多发性骨髓瘤患者的研究。荟萃分析显示客观缓解率(ORR)为87%(95%置信区间[81-93%]),既往接受过靶向B细胞成熟抗原(BCMA)治疗的患者为74%(95%置信区间[65-73%]),未接受过的患者为88%(95%置信区间[78-99%])。部分缓解(PR)为25%,非常好的部分缓解(VGPR)为33%,完全缓解/严格意义上的完全缓解(CR/sCR)为48%,65%的患者实现微小残留病(MRD)阴性。在安全性方面,血液学不良事件(AE)很常见,86%的患者报告有贫血。非血液学常见AE包括细胞因子释放综合征(CRS,83%,5%为≥3级)和低钙血症(63%,10%为≥3级)。未检测到明显的发表偏倚。
GPRC5D是一个活跃且安全的靶点,在复发和/或难治性(R/R)MM以及接受过大量预处理的患者的治疗中显示出有前景的结果。