Miller Kevin, Hashmi Hamza, Rajeeve Sridevi
Myeloma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Front Oncol. 2024 May 10;14:1398902. doi: 10.3389/fonc.2024.1398902. eCollection 2024.
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.
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。