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超越BCMA:多发性骨髓瘤中CAR-T细胞疗法的下一波浪潮。

Beyond BCMA: the next wave of CAR T cell therapy in multiple myeloma.

作者信息

Miller Kevin, Hashmi Hamza, Rajeeve Sridevi

机构信息

Myeloma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, United States.

出版信息

Front Oncol. 2024 May 10;14:1398902. doi: 10.3389/fonc.2024.1398902. eCollection 2024.

Abstract

Chimeric antigen receptor (CAR) T cell therapy has transformed the treatment landscape of relapsed/refractory multiple myeloma. The current Food and Drug Administration approved CAR T cell therapies idecabtagene vicleucel and ciltacabtagene autoleucel both target B cell maturation antigen (BCMA), which is expressed on the surface of malignant plasma cells. Despite deep initial responses in most patients, relapse after anti-BCMA CAR T cell therapy is common. Investigations of acquired resistance to anti-BCMA CAR T cell therapy are underway. Meanwhile, other viable antigenic targets are being pursued, including G protein-coupled receptor class C group 5 member D (GPRC5D), signaling lymphocytic activation molecule family member 7 (SLAMF7), and CD38, among others. CAR T cells targeting these antigens, alone or in combination with anti-BCMA approaches, appear to be highly promising as they move from preclinical studies to early phase clinical trials. This review summarizes the current data with novel CAR T cell targets beyond BCMA that have the potential to enter the treatment landscape in the near future.

摘要

嵌合抗原受体(CAR)T细胞疗法已经改变了复发/难治性多发性骨髓瘤的治疗格局。目前美国食品药品监督管理局批准的CAR T细胞疗法idecabtagene vicleucel和ciltacabtagene autoleucel均靶向B细胞成熟抗原(BCMA),该抗原在恶性浆细胞表面表达。尽管大多数患者最初反应强烈,但抗BCMA CAR T细胞治疗后复发很常见。目前正在对抗BCMA CAR T细胞治疗的获得性耐药进行研究。与此同时,正在寻找其他可行的抗原靶点,包括G蛋白偶联受体C类第5组成员D(GPRC5D)、信号淋巴细胞激活分子家族成员7(SLAMF7)和CD38等。靶向这些抗原的CAR T细胞,单独或与抗BCMA方法联合使用,从临床前研究进入早期临床试验时似乎前景广阔。本综述总结了目前关于BCMA以外新型CAR T细胞靶点的数据,这些靶点有可能在不久的将来进入治疗领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a18/11116580/82026e88fc00/fonc-14-1398902-g001.jpg

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