trk受体
ROS1型
耐受性
医学
受体酪氨酸激酶
肺癌
癌症
癌症研究
药理学
临床试验
内科学
受体
腺癌
不利影响
神经营养素
作者
Christian Rolfo,Rossana Ruiz,Elisa Giovannetti,Ignacio Gil‐Bazo,Antonio Russo,Francesco Passiglia,Marco Giallombardo,Marc Peeters,Luis E. Raez
标识
DOI:10.1517/13543784.2015.1096344
摘要
Among the several experimental drugs under clinical development, entrectinib is emerging as an innovative and promising targeted agent. The encouraging antitumor activity reported in the Phase 1 studies, together with the acceptable toxicity profile, suggest that entrectinib, thanks to its peculiar mechanism of action, could play an important role in the treatment-strategies of multiple TRK-A, B, C, ROS1, and ALK- dependent solid tumors, including NSCLC and colorectal cancer. That being said, further evidence for its clinical use is still needed.
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