Idecabtagene vicleucel for relapsed/refractory multiple myeloma: a review of recent advances

被引:1
|
作者
Tu, Wei [1 ]
Xiao, Yajuan [2 ]
Wang, Yadong [1 ]
Luo, Rongcheng [1 ]
Chen, Zhe-Sheng [3 ,4 ]
机构
[1] Guangzhou Univ Chinese Med, Jinshazhou Hosp, Guangzhou, Peoples R China
[2] Southern Med Univ, Integrated Hosp Tradit Chinese Med, Canc Ctr, Guangzhou, Peoples R China
[3] St Johns Univ, Coll Pharm & Hlth Sci, Dept Pharmaceut Sci, New York, NY 11439 USA
[4] St Johns Univ, Inst Biotechnol, New York, NY USA
关键词
Idecabtagene vicleucel (ide-cel); Multiple  myeloma;   Anti-B-cell maturation antigen (BCMA) agents; CAR-T therapy; Hematologic malignancies; Cancer immunotherapy; Cell-based gene therapy; CELL MATURATION ANTIGEN; T-CELLS; THERAPY; BCMA; GENE; IMMUNOGLOBULIN; LYMPHOCYTES; ANTIBODY; BINDING; TARGET;
D O I
10.1358/dot.2022.58.3.3381592
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The introduction of new classes of drugs for the treatment of multiple myeloma (MM) in the past 2 decades, such as proteasome inhibitors, immunomodulators and anti-CD38 monoclonal antibodies, coupled with autologous stem cell transplantation, has approximately doubled the 5-year survival rate of MM patients. However, the patients eventually relapse and/or become resistant to the drugs and treatment. The recent emergence of anti-B-cell maturation antigen (BCMA) therapies, especially chimeric antigen receptor T-cell (CAR-T) immunotherapy targeting BCMA, holds great prospect in MM treatment. In this article, we review in detail the advances of idecabtagene vicleucel (ide-cel, bb-2121), the first CAR-T therapy targeting BCMA for treating relapse or refractory MM approved by the U.S. Food and Drug Administration (FDA) in 2021, including the preclinical study and phase I and II clinical trials. Also, it is predicted in this review that despite its amazing clinical efficacy and relatively lower toxicity, a lot of challenges and unsolved problems for ide-cel therapy remain in the way ahead.
引用
收藏
页码:117 / 132
页数:16
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