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用于非小细胞肺癌的表皮生长因子受体酪氨酸激酶抑制剂

Epidermal growth factor receptor tyrosine kinase inhibitors for non-small cell lung cancer.

作者信息

Asami Kazuhiro, Atagi Shinji

机构信息

Kazuhiro Asami, Shinji Atagi, Department of Clinical Oncology, National Hospital Organization Kinki-chuo Chest Medical Center, Sakai City, Osaka 591-8555, Japan.

出版信息

World J Clin Oncol. 2014 Oct 10;5(4):646-59. doi: 10.5306/wjco.v5.i4.646.

Abstract

First-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), including gefitinib and erlotinib, have proven to be highly effective agents for advanced non-small cell lung cancer (NSCLC) in patients harboring an activating EGFR mutation such as the exon 19 deletion mutation and L858R. Although those reversible small molecular targeted agents provide a significant response and survival benefit, all responders eventually acquire resistance. Second-generation EGFR-targeting agents, such as irreversible EGFR/HER2 tyrosine kinase inhibitors and pan-HER TKIs, may improve survival further and be useful for patients who acquired resistance to first-generation EGFR-TKIs. This review discusses novel therapeutic strategies for EGFR-mutated advanced NSCLC using first- and second-generation EGFR-TKIs.

摘要

第一代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs),包括吉非替尼和厄洛替尼,已被证明是治疗晚期非小细胞肺癌(NSCLC)的高效药物,适用于携带激活型EGFR突变(如外显子19缺失突变和L858R)的患者。尽管这些可逆性小分子靶向药物能带来显著疗效和生存获益,但所有有反应的患者最终都会产生耐药性。第二代EGFR靶向药物,如不可逆性EGFR/HER2酪氨酸激酶抑制剂和泛HER TKIs,可能会进一步提高生存率,对第一代EGFR-TKIs耐药的患者可能有用。本文综述了使用第一代和第二代EGFR-TKIs治疗EGFR突变型晚期NSCLC的新型治疗策略。

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