New and emerging pharmacotherapies for the management of multiple myeloma

被引:5
作者
Moore, Donald C. [1 ]
Oxencis, Carolyn J. [2 ]
Shank, Brandon R. [3 ]
机构
[1] Atrium Hlth, Dept Pharm, Levine Canc Inst, Charlotte, NC 28203 USA
[2] Froedtert & Med Coll Wisconsin, Milwaukee, WI USA
[3] Univ Texas MD Anderson Canc Ctr, Div Pharm, Houston, TX 77030 USA
关键词
bispecific antibodies; CAR T-cell therapy; monoclonal antibodies; multiple myeloma; CELL MATURATION ANTIGEN; OPEN-LABEL; NUCLEAR EXPORT; T-CELLS; TARGET; TRANSPLANTATION; DEXAMETHASONE; MULTICENTER; DARATUMUMAB; BORTEZOMIB;
D O I
10.1093/ajhp/zxac091
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose The pharmacology, efficacy, safety, and dosing/administration of new and emerging therapies for the treatment of multiple myeloma are summarized. There have been significant advancements in the treatment of multiple myeloma in recent years, with an expansion of available drug therapies. Newer therapies for multiple myeloma include the anti-CD38 monoclonal antibodies daratumumab and isatuximab, the exportin 1 inhibitor selinexor, the anti-B-cell maturation antigen (BCMA) antibody-drug conjugate belantamab mafodotin, and the chimeric antigen receptor (CAR) T-cell therapy idecabtagene vicleucel. These agents have unique toxicity profiles, specific monitoring parameters, and operational considerations that clinicians treating multiple myeloma should be aware of. There is likely to be continued rapid expansion of new agents for patients with multiple myeloma, as there are many novel investigational agents in the drug development pipeline, such as bispecific antibodies and additional CAR T-cell therapies. Conclusion Several therapeutic agents have been recently approved by the Food and Drug Administration for the treatment of multiple myeloma. There are many novel agents in the pipeline, including bispecific antibodies and CAR T-cell therapies that have the potential to continue to change the treatment landscape of multiple myeloma.
引用
收藏
页码:1137 / 1145
页数:9
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