Spotlight on ixazomib: potential in the treatment of multiple myeloma

被引:103
作者
Muz, Barbara [1 ]
Ghazarian, Rachel Nicole [1 ,2 ]
Ou, Monica [1 ,3 ]
Luderer, Micah John [1 ]
Kusdono, Hubert Daniel [1 ,2 ]
Azab, Abdel Kareem [1 ]
机构
[1] Washington Univ, Sch Med, Div Canc Biol, Dept Radiat Oncol, St Louis, MO 63108 USA
[2] St Louis Univ, St Louis Coll Pharm, Dept Pharmaceut & Adm Sci, St Louis, MO 63103 USA
[3] St Louis Univ, Dept Biol, St Louis, MO 63103 USA
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2016年 / 10卷
基金
美国国家卫生研究院;
关键词
proteasome inhibitor; oral administration; biological mechanism; clinical trials; PROTEASOME INHIBITOR MLN9708; BONE-MARROW MICROENVIRONMENT; BORTEZOMIB; CELLS; THERAPY; DEXAMETHASONE; GLYCOPROTEIN; CARFILZOMIB; DISEASE; CONTEXT;
D O I
10.2147/DDDT.S93602
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Despite the significant therapeutic advances achieved with proteasome inhibitors (PIs) such as bortezomib and carfilzomib in prolonging the survival of patients with multiple myeloma, the development of drug resistance, peripheral neuropathy, and pharmacokinetic limitations continue to pose major challenges when using these compounds. Ixazomib is a second-generation PI with improved activity over other PIs. Unlike bortezomib and carfilzomib, which are administered by injection, ixazomib is the first oral PI approved by US Food and Drug Administration. This review discusses the biochemical properties, mechanisms of action, preclinical efficacy, and clinical trial results leading to the US Food and Drug Administration approval of ixazomib.
引用
收藏
页码:217 / 226
页数:10
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