作者: Stephen V Liu , Deepa Subramaniam , George C Cyriac , Feras J Abdul-Khalek , Giuseppe Giaccone
DOI: 10.1517/14728214.2014.873403
关键词: Protein kinase A 、 Oncology 、 Dacomitinib 、 Targeted therapy 、 Cancer research 、 KRAS 、 Medicine 、 Anaplastic lymphoma kinase 、 Epidermal growth factor receptor 、 Kinase 、 ROS1 、 Internal medicine 、 Pharmacology (medical) 、 Pharmacology
摘要: Introduction: In the current paradigm of precision medicine in non-small cell lung cancer (NSCLC), therapeutic strategy is determined by molecular characteristics. The best examples this approach are kinase inhibitors that selectively target tumors bearing an epidermal growth factor receptor (EGFR) mutation or anaplastic lymphoma (ALK) rearrangement. Emerging protein may enhance our ability to effectively treat these and other genomic subtypes NSCLC. Areas covered: This article reviews next-generation targeting EGFR ALK-positive addition, targeted clinical development for specific NSCLC covered, including ROS1, BRAF, RET, HER2, KRAS (upstream MEK kinase), MET, PIK3CA, FGFR1, DDR2, VEGFR AAK. Expert opinion: EGFR-mutant NSCLC, there several with promising activity, most notably dacomitinib CO-1686 acquired resistance to...