克里唑蒂尼
ROS1型
间变性淋巴瘤激酶
医学
癌症研究
突变
腺癌
碱性抑制剂
肺癌
遗传学
肿瘤科
癌症
内科学
生物
基因
恶性胸腔积液
作者
Mark M. Awad,Ryohei Katayama,Michele McTigue,Wei Liu,Ya-Li Deng,Alexei Brooun,Luc Friboulet,Donghui Huang,Matthew D. Falk,Sergei Timofeevski,Keith D. Wilner,Elizabeth L. Lockerman,Tahsin Khan,Sidra Mahmood,Justin F. Gainor,Subba R. Digumarthy,James R. Stone,Mari Mino–Kenudson,James G. Christensen,A. John Iafrate
标识
DOI:10.1056/nejmoa1215530
摘要
Crizotinib, an inhibitor of anaplastic lymphoma kinase (ALK), has also recently shown efficacy in the treatment of lung cancers with ROS1 translocations. Resistance to crizotinib developed in a patient with metastatic lung adenocarcinoma harboring a CD74-ROS1 rearrangement who had initially shown a dramatic response to treatment. We performed a biopsy of a resistant tumor and identified an acquired mutation leading to a glycine-to-arginine substitution at codon 2032 in the ROS1 kinase domain. Although this mutation does not lie at the gatekeeper residue, it confers resistance to ROS1 kinase inhibition through steric interference with drug binding. The same resistance mutation was observed at all the metastatic sites that were examined at autopsy, suggesting that this mutation was an early event in the clonal evolution of resistance. (Funded by Pfizer and others; ClinicalTrials.gov number, NCT00585195.).
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