首页> 美国卫生研究院文献>ESMO Open >Phase II study of erlotinib plus tivantinib (ARQ 197) in patients with locally advanced or metastatic EGFR mutation-positive non-small-cell lung cancer just after progression on EGFR-TKI gefitinib or erlotinib
【2h】

Phase II study of erlotinib plus tivantinib (ARQ 197) in patients with locally advanced or metastatic EGFR mutation-positive non-small-cell lung cancer just after progression on EGFR-TKI gefitinib or erlotinib

机译:EGFR-TKI吉非替尼或厄洛替尼治疗进展后厄洛替尼联合依维替尼(ARQ 197)在患有局部晚期或转移性EGFR突变阳性的非小细胞肺癌患者中进行的II期研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BackgroundPatients with epidermal growth factor receptor (EGFR) activation mutation-positive non-small-cell lung cancer (NSCLC) respond well to EGFR tyrosine kinase inhibitors (EGFR-TKIs), but eventually become resistant in most cases. The hepatocyte growth factor/c-Met (HGF/c-Met) pathway is reported as a poor prognostic factor in various cancers. As c-Met is involved in EGFR-TKI resistance, a c-Met inhibitor and EGFR-TKI combination may reverse the resistance. This study evaluated the efficacy and safety of a c-Met selective inhibitor, tivantinib (ARQ 197), in combination with erlotinib, in Japanese EGFR mutation-positive patients with NSCLC who progressed while on EGFR-TKIs.
机译:背景具有表皮生长因子受体(EGFR)激活突变阳性的非小细胞肺癌(NSCLC)的患者对EGFR酪氨酸激酶抑制剂(EGFR-TKIs)的反应良好,但最终在大多数情况下具有耐药性。据报道,肝细胞生长因子/ c-Met(HGF / c-Met)途径是各种癌症中不良的预后因素。由于c-Met参与EGFR-TKI耐药性,因此c-Met抑制剂和EGFR-TKI组合可逆转耐药性。这项研究评估了c-Met选择性抑制剂tivantinib(ARQ 197)与厄洛替尼联合在日本EGFR突变阳性NSCLC患者中的疗效和安全性,这些患者在EGFR-TKIs上进展。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号