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解决非小细胞肺癌中表皮生长因子受体酪氨酸激酶抑制剂耐药问题。

Addressing epidermal growth factor receptor tyrosine kinase inhibitor resistance in non-small cell lung cancer.

作者信息

Noda Shoko, Kanda Shintaro

机构信息

a Department of Thoracic Oncology , National Cancer Center Hospital , Tokyo , Japan.

出版信息

Expert Rev Respir Med. 2016;10(5):547-56. doi: 10.1586/17476348.2016.1164603. Epub 2016 Mar 28.

Abstract

Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) have significantly improved the survival of patients with advanced non-small cell lung cancer (NSCLC) harboring EGFR activating mutations. However, nearly all EGFR-mutant NSCLC tumors eventually acquire resistance to the currently used EGFR-TKIs and subsequently progress clinically. Acquired resistance to EGFR-TKIs is thus a huge issue in the treatment of EGFR-mutant NSCLC at present. On one hand, T790M second-site mutation has been recognized as a key mechanism of EGFR-TKI resistance, and third generation EGFR-TKIs such as osimertinib and rociletinib have been developed to overcome tumor cells harboring the T790M mutation. On the other hand, combination with cytotoxic chemotherapy is also expected as another strategy for preventing the acquired resistance to current EGFR-TKIs and prolonging the survival benefits by EGFR-TKIs. Here, we review updated strategies for preventing or overcoming acquired resistance to EGFR-TKIs.

摘要

表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)显著提高了携带EGFR激活突变的晚期非小细胞肺癌(NSCLC)患者的生存率。然而,几乎所有EGFR突变的NSCLC肿瘤最终都会对目前使用的EGFR-TKIs产生耐药性,并随后在临床上进展。因此,获得性EGFR-TKIs耐药是目前EGFR突变NSCLC治疗中的一个巨大问题。一方面,T790M二次位点突变已被认为是EGFR-TKI耐药的关键机制,并且已经开发出第三代EGFR-TKIs,如奥希替尼和罗西替尼,以克服携带T790M突变的肿瘤细胞。另一方面,联合细胞毒性化疗也有望作为预防当前EGFR-TKIs获得性耐药和延长EGFR-TKIs生存获益的另一种策略。在此,我们综述了预防或克服EGFR-TKIs获得性耐药的最新策略。

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