Trastuzumab emtansine: a novel antibody-drug conjugate for HER2-positive breast cancer

被引:26
作者
Burris, Howard A., III [1 ]
机构
[1] Sarah Cannon Res Inst, Nashville, TN 37203 USA
关键词
GROWTH-FACTOR RECEPTOR; CLINICAL-PRACTICE GUIDELINES; BRAIN METASTASES; CARDIAC SAFETY; PHASE-II; LAPATINIB; COMBINATION; T-DM1; PROGRESSION; EFFICACY;
D O I
10.1517/14712598.2011.580273
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
Areas covered: The mechanisms of action, preclinical efficacy and clinical profile of T-DM1 are reported. The latest preclinical and clinical data for T-DM1 are examined. Expert opinion: T-DM1 has significant antitumor potency in vitro and in vivo, which is maintained in tumors resistant to trastuzumab or lapatinib. In Phase I and II trials, T-DM1 provided objective tumor responses and was well tolerated across various lines of therapy in patients with HER2-positive MBC. In addition, it showed similar efficacy to trastuzumab plus docetaxel in first-line MBC. Ongoing trials (including two Phase III studies) are investigating T-DM1 as single-agent therapy or combined with other chemotherapeutic or biologic agents, and the results should help to define the place of T-DM1 within current treatment algorithms for HER2-positive disease.
引用
收藏
页码:807 / 819
页数:13
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