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克唑替尼获得性耐药与 CD74-ROS1 突变有关。

Acquired resistance to crizotinib from a mutation in CD74-ROS1.

机构信息

Department of Medicine, Massachusetts General Hospital Cancer Center, Boston, MA 02114, USA.

出版信息

N Engl J Med. 2013 Jun 20;368(25):2395-401. doi: 10.1056/NEJMoa1215530. Epub 2013 Jun 1.

Abstract

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.).

摘要

克唑替尼是一种间变性淋巴瘤激酶(ALK)抑制剂,最近也显示出在治疗具有 ROS1 易位的肺癌方面的疗效。一名患有携带 CD74-ROS1 重排的转移性肺腺癌的患者对克唑替尼产生了耐药性,该患者最初对治疗有明显反应。我们对耐药性肿瘤进行了活检,并发现了一个获得性突变,导致 ROS1 激酶结构域中的 2032 密码子的甘氨酸到精氨酸取代。尽管该突变不在守门员残基处,但它通过与药物结合的空间位阻干扰导致对 ROS1 激酶抑制的耐药性。在尸检检查的所有转移性部位均观察到相同的耐药性突变,表明该突变是耐药性克隆进化中的早期事件。(由辉瑞等资助;ClinicalTrials.gov 编号,NCT00585195.)。

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