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

被引:6
作者
Miller, Kevin [1 ]
Hashmi, Hamza [1 ]
Rajeeve, Sridevi [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Myeloma Serv, New York, NY 10065 USA
关键词
multiple myeloma; CAR T cell therapy; chimeric antigen receptor; non-BCMA; immunotherapy; CHIMERIC ANTIGEN RECEPTOR; PROTEIN-COUPLED RECEPTOR; MATURATION ANTIGEN; BONE-MARROW; PHASE; 1B/2; SINGLE-ARM; CD38; IMMUNOTHERAPY; TARGET; DARATUMUMAB;
D O I
10.3389/fonc.2024.1398902
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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收藏
页数:13
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