Carfilzomib in multiple myeloma

被引:15
|
作者
Andreu-Vieyra, Claudia [1 ]
Berenson, James R. [1 ,2 ,3 ]
机构
[1] Oncotherapeutics, West Hollywood, CA USA
[2] Inst Myeloma & Bone Canc Res, West Hollywood, CA 90069 USA
[3] James R Berenson MD Inc, West Hollywood, CA USA
关键词
carfilzomib; epoxyketone class; multiple myeloma; proteasome inhibitor; SINGLE-AGENT CARFILZOMIB; LOW-DOSE DEXAMETHASONE; PROTEASOME INHIBITOR CARFILZOMIB; BORTEZOMIB-MELPHALAN-PREDNISONE; THALIDOMIDE PLUS DEXAMETHASONE; STEM-CELL TRANSPLANTATION; PERIPHERAL NEUROPATHY; INITIAL TREATMENT; IRREVERSIBLE INHIBITOR; MOLECULAR-BASIS;
D O I
10.1517/14712598.2014.953050
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Advances in drug therapy for multiple myeloma (MM) during the previous decade have improved survival outcomes; however, the disease remains incurable as patients eventually relapse or become refractory to all available therapies. Therefore, there is a clear need for more effective and well-tolerated treatments. Areas covered: We review preclinical and clinical data regarding the use of carfilzomib, a proteasome inhibitor that is structurally and mechanistically distinct from bortezomib, for the treatment of MM patients. Carfilzomib pharmacokinetics, pharmacodynamics, efficacy, safety and tolerability are summarized, based on Phase I/II trial data. Expert opinion: Carfilzomib represents a significant advance in the management of relapsed and/or refractory MM patients, including those intolerant or resistant to bortezomib. High response rates have been demonstrated with carfilzomib as a single agent or in combination with alkylating agents, immunomodulators and corticosteroids, even among patients who have failed multiple prior therapies. Carfilzomib also has significant potential in the frontline setting, with encouraging response and survival rates observed for combination regimens. Further evaluation of carfilzomib-containing regimens is ongoing in Phase III trials and investigator-sponsored studies, which include combinations with novel investigational agents. These findings will shape the future role of carfilzomib for MM patients across multiple settings.
引用
收藏
页码:1685 / 1699
页数:15
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