Emerging agents and regimens for multiple myeloma

被引:61
|
作者
Yang, Yang [1 ]
Li, Yi [1 ]
Gu, Huiyao [1 ]
Dong, Mengmeng [1 ]
Cai, Zhen [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Bone Marrow Transplantat Ctr,Dept Hematol, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Hematol, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Med Ctr, Zhejiang Lab Syst & Precis Med, Hangzhou, Zhejiang, Peoples R China
关键词
Multiple myeloma; Monoclonal antibody; Immunotherapy; Checkpoint inhibitor; BiTE; CAR-T; STEM-CELL TRANSPLANTATION; LOW-DOSE DEXAMETHASONE; OPEN-LABEL; T-CELLS; PHASE-III; DOUBLE-BLIND; DARATUMUMAB MONOTHERAPY; CLINICAL-RESPONSES; MATURATION ANTIGEN; PLUS POMALIDOMIDE;
D O I
10.1186/s13045-020-00980-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The outcomes of multiple myeloma (MM) have been improved significantly with the therapies incorporating proteasome inhibitors (PI), immunomodulatory drugs, monoclonal antibodies (MoAb) and stem cell transplantation. However, relapsed and refractory MM (RRMM) remains a major challenge. Novel agents and regimens are under active clinical development. These include new PIs such as ixazomib, marizomib, and oprozomib; new MoAbs such as isatuximab and MOR202; novel epigenetic agent ricolinostat and novel cytokines such as siltuximab. Recently, the first XPO-1 inhibitor, selinexor, was approved for RRMM. BCMA-targeted BiTE, antibody-drug conjugates and CAR-T cells have the potential to revolutionize the therapy for RRMM. In this review, we summarized the latest clinical development of these novel agents and regimens.
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页数:25
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