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Navigating the No Mans Land of TKI-Failed EGFR-Mutated Non–Small Cell Lung Cancer (NSCLC): A Review

机译:穿越TKI失败的EGFR突变的非小细胞肺癌(NSCLC)的无人区:综述

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摘要

As the leading cause of cancer-related mortality, lung cancer is a worldwide health issue that is overwhelmingly caused by smoking. However, a substantial minority (~25%) of patients with non–small cell lung cancer (NSCLC) has never smoked. In these patients, activating mutations of the epidermal growth factor receptor (EGFR) are more likely, which render their tumors susceptible for a finite period to treatment with EGFR tyrosine kinase inhibitors (TKIs) and confer a better prognosis than EGFR wild-type NSCLC. On progression, due to the inevitable insurgence of resistance, TKIs are generally followed by second- or third-line salvage chemotherapy until treatment failure, after which no standard treatment options are available, resulting in a poor prognosis and a high risk of death. With the focus of clinical attention on treatment with TKIs, few studies on optimal salvage therapies, including cytotoxic chemotherapy, after failure of EGFR TKIs have been reported. Despite a paucity of available data, the aim of this review is to summarize the “no-man's land” of TKI-failed EGFR-mutated NSCLC and expand on alternative strategies as well as potential future directions.
机译:作为癌症相关死亡率的主要原因,肺癌是世界范围内的健康问题,绝大多数由吸烟引起。但是,非小细胞肺癌(NSCLC)的绝大部分患者(约25%)从未吸烟。在这些患者中,表皮生长因子受体(EGFR)的激活突变更可能发生,这使他们的肿瘤在有限的时期内易于接受EGFR酪氨酸激酶抑制剂(TKI)的治疗,并且预后比EGFR野生型NSCLC更好。在进展过程中,由于不可避免地产生耐药性,通常在进行TKI疗法后进行二线或三线挽救性化疗,直到治疗失败为止,此后没有可用的标准治疗方案,导致预后不良和高死亡风险。由于临床上将重点放在TKIs的治疗上,很少有关于EGFR TKIs失效后最佳挽救疗法包括细胞毒性化学疗法的研究的报道。尽管缺乏可用数据,但本综述的目的是总结TKI失败的EGFR突变的NSCLC的“无人区”,并扩展替代策略以及潜在的未来方向。

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