Future of CAR T cells in multiple myeloma

被引:24
|
作者
Wudhikarn, Kitsada [1 ,2 ]
Mailankody, Sham [3 ,4 ,5 ]
Smith, Eric L. [6 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[2] Chulalongkorn Univ, Dept Med, Res Unit Translat Hematol, Bangkok, Thailand
[3] Mem Sloan Kettering Canc Ctr, Myeloma Serv, Dept Med, 1275 York Ave, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Cellular Therapeut Ctr, 1275 York Ave, New York, NY 10021 USA
[5] Weill Cornell Med Coll, Dept Med, New York, NY USA
[6] Harvard Med Sch, Dept Med Oncol, Dana Farber Canc Inst, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
MINIMAL RESIDUAL DISEASE; THERAPY; ANTIGEN; BCMA; IMMUNOTHERAPY; OUTCOMES;
D O I
10.1182/hematology.2020000111
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Despite the significant improvement in survival outcomes of multiple myeloma (MM) over the past decade, it remains an incurable disease. Patients with triple-class refractory MM have limited treatment options and a dismal prognosis. Chimeric antigen receptor (CAR) T-cell therapy targeting B-cell maturation antigen has transformed the treatment armamentarium of relapsed/refractory MM (RRMM), with unprecedented overall response rates in this difficult-to-treat patient population. However, a significant proportion of patients ultimately relapse despite achieving deep remission. Several innovative approaches, including alternative/dual-antigen-specific CAR T-cell constructs, genetically engineered "off-the-shelf" CAR T cells, and strategies to counteract an immunosuppressive microenvironment, may dramatically reshape the field of CAR T-cell therapy in the future. These strategies are being actively investigated in preclinical and early clinical trial settings with the hopes of enhancing the durability of responses and, thereby, improving the overall survival of RRMM patients after CAR T-cell therapy.
引用
收藏
页码:272 / 279
页数:8
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