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优化 EGFR 突变阳性 NSCLC 的治疗结局:应选择哪种酪氨酸激酶抑制剂及何时使用?

Optimizing outcomes in EGFR mutation-positive NSCLC: which tyrosine kinase inhibitor and when?

机构信息

Thoracic Oncology, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, 69622, France.

Thoracic Surgery, Institut Curie, Institut du Thorax Curie-Montsouris, Paris, 75248, France.

出版信息

Future Oncol. 2018 May;14(11):1117-1132. doi: 10.2217/fon-2017-0636. Epub 2018 Jan 16.

Abstract

Despite the efficacy of standard-of-care EGFR tyrosine kinase inhibitors (TKIs), erlotinib, gefitinib and afatinib, in EGFR mutation-positive non-small-cell lung cancer, resistance develops, most commonly due to the T790M mutation. Osimertinib showed clinical activity in the treatment of T790M-positive disease following progression on a first-line TKI, and is approved in this setting. Recently, osimertinib improved efficacy versus first-generation TKIs (erlotinib and gefitinib) in the first-line setting. Multiple factors can influence first-line treatment decisions, including subsequent therapy options, presence of brain metastases and tolerability, all of which should be considered in the long-term treatment plan. Further research into treatment sequencing is also needed, to optimize outcomes in EGFR mutation-positive non-small-cell lung cancer.

摘要

尽管标准护理表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs),如厄洛替尼、吉非替尼和阿法替尼,在 EGFR 突变阳性的非小细胞肺癌中具有疗效,但耐药性还是会出现,最常见的原因是 T790M 突变。奥希替尼在一线 TKI 治疗进展后治疗 T790M 阳性疾病显示出临床活性,并且在该治疗环境中得到批准。最近,奥希替尼在一线治疗中优于第一代 EGFR-TKIs(厄洛替尼和吉非替尼)。多种因素会影响一线治疗决策,包括后续治疗选择、脑转移的存在和耐受性,所有这些都应在长期治疗计划中考虑。还需要进一步研究治疗顺序,以优化 EGFR 突变阳性非小细胞肺癌的治疗结果。

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