Emerging Treatments for Multiple Myeloma: Beyond Immunomodulatory Drugs and Bortezomib

被引:50
作者
Mitsiades, Constantine S. [1 ]
Hideshima, Teru [1 ]
Chauhan, Dharminder [1 ]
McMillin, Douglas W. [1 ]
Klippel, Steffen [1 ]
Laubach, Jacob P. [1 ]
Munshi, Nikhil C. [1 ]
Anderson, Kenneth C. [1 ]
Richardson, Paul G. [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Jerome Lipper Multiple Myeloma Ctr,Dept Med Oncol, Boston, MA 02115 USA
关键词
SUBEROYLANILIDE HYDROXAMIC ACID; HISTONE DEACETYLASE INHIBITOR; PHASE-I TRIAL; UNFOLDED PROTEIN RESPONSE; NF-KAPPA-B; PROTEASOME INHIBITOR; HSP90; INHIBITOR; CLINICAL-TRIAL; IRREVERSIBLE INHIBITOR; MOLECULAR SEQUELAE;
D O I
10.1053/j.seminhematol.2009.02.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The successful clinical development of thalidomide, bortezomib, and lenalidomide not only transformed the therapeutic management of multiple myeloma (MM) but also catalyzed a renewed interest in the development of additional classes of novel agents for this disease. This review focuses on I series of new therapeutics that have shown promising preclinical results, its well as encouraging safety profiles and early evidence of anti-MM activity in clinical studies, either alone or in combination with other, conventional or novel, anti-MM treatments. These agents include second-generation proteasome inhibitors and immunomodulatory agents, is well as members of other therapeutic classes, such as histone deacetylase inhibitors (HDAC), heat shock protein 90 (Hsp90) inhibitors, and the alkylphospholipid Akt inhibitor perifosine. Semin Hematol 46:166-175. (C) 2009 Published by Elsevier Inc.
引用
收藏
页码:166 / 175
页数:10
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