Novel agents in the treatment of multiple myeloma: a review about the future

被引:146
作者
Naymagon, Leonard [1 ]
Abdul-Hay, Maher [1 ,2 ,3 ]
机构
[1] NYU, Dept Med, 550 1St Ave, New York, NY 10016 USA
[2] NYU, Perlmutter Canc Ctr, New York, NY USA
[3] NYU, Sch Med, 240 East 38th St,19 Floor, New York, NY 10016 USA
来源
JOURNAL OF HEMATOLOGY & ONCOLOGY | 2016年 / 9卷
关键词
Multiple myeloma; Novel agents; Immunomodulators; Proteasome inhibitors; Alkylating agents; AKT inhibitors; BTK inhibitors; CDK inhibitors; HDACIs; IL-6; inhibitors; Kinesin spindle protein inhibitors; Monoclonal antibodies; PI3K inhibitors; ORAL PROTEASOME INHIBITOR; LOW-DOSE DEXAMETHASONE; LENALIDOMIDE PLUS DEXAMETHASONE; PI3K INHIBITOR; OPEN-LABEL; PHASE-II; INTERGROUPE FRANCOPHONE; DARATUMUMAB MONOTHERAPY; SILTUXIMAB ANTI-IL-6; PRECLINICAL ACTIVITY;
D O I
10.1186/s13045-016-0282-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma (MM) is a disease that affects plasma cells and can lead to devastating clinical features such as anemia, lytic bone lesions, hypercalcemia, and renal disease. An enhanced understanding of MM disease mechanisms has led to new more targeted treatments. There is now a plethora of treatments available for MM. In this review article, our aim is to discuss many of the novel agents that are being studied or have recently been approved for the treatment of MM. These agents include the following: immunomodulators (pomalidomide), proteasome inhibitors (carfilzomib, marizomib, ixazomib, oprozomib), alkylating agents (bendamustine), AKT inhibitors (afuresertib), BTK inhibitors (ibrutinib), CDK inhibitors (dinaciclib), histone deacetylase inhibitors (panobinostat, rocilinostat, vorinostat), IL-6 inhibitors (siltuximab), kinesin spindle protein inhibitors (filanesib), monoclonal antibodies (daratumumab, elotuzumab, indatuximab, SAR650984), and phosphoinositide 3-kinase (PI3K) inhibitors.
引用
收藏
页数:20
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