【不可逆EGFR-TKI在非小细胞肺癌中的研究现状及未来发展方向】。

M X Fang, W D Wu, X X Yu
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引用次数: 0

摘要

表皮生长因子受体酪氨酸激酶抑制剂(EGFR- tki)是治疗EGFR突变型非小细胞肺癌(NSCLC)的重要药物。然而,第一代和第二代EGFR-TKI由于获得性耐药(如T790M突变)而面临临床局限性。不可逆EGFR-TKI通过共价结合机制增强对耐药突变的抑制,显著延长患者生存期。本文系统综述了不可逆EGFR-TKI的作用机制、临床研究进展及未来发展方向,重点介绍了其在克服耐药方面的潜力、联合治疗策略以及生物标志物引导下的个性化治疗,以期为临床实践提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Research status and future direction of irreversible EGFR-TKI in non-small cell lung cancer].

Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKI) are important treatments for EGFR mutant non-small cell lung cancer (NSCLC). However, the first and second generation EGFR-TKI face clinical limitations due to acquired resistance, such as the T790M mutation. Irreversible EGFR-TKI can significantly prolong the survival of patients by enhancing the inhibition of drug-resistant mutations through the covalent binding mechanism. This article systematically reviews the mechanism of action, clinical research progress and future direction of irreversible EGFR-TKI, focusing on their potential to overcome drug resistance, combination treatment strategies and biomarker guided personalized treatment, in order to provide references for clinical practice.

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