Proteasome inhibitors in the treatment of multiple myeloma

被引:7
|
作者
McBride, Ali [1 ,2 ,3 ]
Ryan, Patricia Y. [4 ]
机构
[1] James Canc Hosp, Columbus, OH 43210 USA
[2] Solove Res Inst, Columbus, OH 43210 USA
[3] Ohio State Univ, Columbus, OH 43210 USA
[4] Millennium Pharmaceut Inc, Cambridge, MA USA
关键词
bortezomib; carfilzomib; marizomib; MLN9708; multiple myeloma; peripheral neuropathy; proteasome inhibitors; STEM-CELL TRANSPLANTATION; RANDOMIZED PHASE-III; BORTEZOMIB-MELPHALAN-PREDNISONE; SINGLE-AGENT CARFILZOMIB; THALIDOMIDE PLUS DEXAMETHASONE; EXTENDED FOLLOW-UP; PERIPHERAL NEUROPATHY; MAINTENANCE THERAPY; COMBINATION THERAPY; INDUCTION THERAPY;
D O I
10.1586/ERA.13.9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Proteasome inhibition has been shown to be an effective strategy for the treatment of multiple myeloma, as demonstrated by the clinical activity of the first-in-class agent bortezomib. Recently, the second-generation proteasome inhibitor carfilzomib has been approved in the USA in the relapsed and refractory setting, and several other investigational agents are in clinical development, including MLN9708, marizomib, oprozomib and delanzomib. Here, the authors provide a comprehensive review of the key role of proteasome inhibitors in the myeloma treatment pathway, and highlight the similarities and differences in pharmacology, routes of administration, and efficacy and safety profiles between bortezomib, carfilzomib and investigational agents. The authors also evaluate the potential for further improving myeloma treatment through the ongoing development of novel proteasome inhibitors.
引用
收藏
页码:339 / 358
页数:20
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