埃罗替尼
医学
临床试验
肺癌
重症监护医学
肿瘤科
个性化医疗
癌症
内科学
表皮生长因子受体
生物信息学
生物
作者
Christian Rolfo,Nele Van Der Steen,Patrick Pauwels,Federico Cappuzzo
标识
DOI:10.1586/14737140.2015.1031219
摘要
The development of targeted therapies has led to a revolution in non-small-cell lung cancer, and opened up possibilities for improved personalized medicine. With the constant findings of new targets, a lot of inhibitors are being developed. However, reliable biomarkers are urgently needed. The design of clinical trials needs to become more flexible in order to obtain the best results and gain the US FDA/EMEA approval for the new drugs. A recent example of a failed trial is the Phase III MetLung trial that compared the effects of the c-MET monovalent antibody onartuzumab with erlotinib versus erlotinib alone in late-stage non-small-cell lung cancer. Here, we discuss several points as to why this trial could have failed.
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