作者: Zengjun Dong , Tienian Zhu , Luting Xu , Ruijing Zhao
DOI: 10.3779/J.ISSN.1009-3419.2013.12.09
关键词: Gene rearrangement 、 Internal medicine 、 Oncology 、 Crizotinib 、 Cancer research 、 Lung cancer 、 Anaplastic lymphoma kinase 、 ROS1 、 Fusion gene 、 Adenocarcinoma 、 Biology 、 Carcinoma
摘要: Chromosomal rearrangements involving the ROS1 receptor tyrosine kinase gene have recently been described in multiple malignancies, including non-small cell lung cancer (NSCLC). rearrangement defines a new molecular subset of NSCLC with prevalence around 1%-2%. ROS1-positive NSCLCs arise young never-smokers adenocarcinoma that are similar to those observed patients ALK-rearranged NSCLC. Crizotinib demonstrates vitro activity and early clinical trial shows marked antitumor ROS1-rearranged patients. The overall response rate is 56% disease control at 8 weeks about 76%. Further understanding fusions pathogenesis NSCLC, methods detect rearrangements, targeting specific inhibitors would lead an era personalized medicine.