Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer

被引:0
|
作者
Teemu T. Junttila
Guangmin Li
Kathryn Parsons
Gail Lewis Phillips
Mark X. Sliwkowski
机构
[1] Genentech,Research Oncology
[2] Inc.,undefined
来源
Breast Cancer Research and Treatment | 2011年 / 128卷
关键词
Breast cancer; HER2; ErbB2; Trastuzumab; Therapeutic antibodies; Antibody drug conjugate (ADC); Trastuzumab-DM1 (T-DM1);
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学科分类号
摘要
Trastuzumab (Herceptin®) is currently used as a treatment for patients whose breast tumors overexpress HER2/ErbB2. Trastuzumab-DM1 (T-DM1, trastuzumab emtansine) is designed to combine the clinical benefits of trastuzumab with a potent microtubule-disrupting drug, DM1 (a maytansine derivative). Currently T-DM1 is being tested in multiple clinical trials. The mechanisms of action for trastuzumab include inhibition of PI3K/AKT signaling pathway, inhibition of HER-2 shedding and Fcγ receptor mediated engagement of immune cells, which may result in antibody-dependent cellular cytotoxicity (ADCC). Here we report that T-DM1 retains the mechanisms of action of unconjugated trastuzumab and is active against lapatinib resistant cell lines and tumors.
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页码:347 / 356
页数:9
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