EGFR突变阳性NSCLC从第一代或第二代EGFR- tki切换到奥西替尼。

Pub Date : 2020-03-19 DOI:10.2217/lmt-2020-0005
Fumio Imamura, Takako Inoue, Kei Kunimasa, Aki Kubota, Hanako Kuhara, Motohiro Tamiya, Kazumi Nishino, Madoka Kimura, Kika Kuno, Hayato Kawachi, Toru Kumagai
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引用次数: 4

摘要

目的:我们评估了一种新的EGFR- tkis开关方案对EGFR突变阳性NSCLC的疗效。材料与方法:从接受两种EGFR-TKI顺序联合策略之一的患者中收集临床记录:挽救使用奥西替尼治疗t790m介导的对先前EGFR-TKI的获得性耐药,或在疾病进展前将EGFR-TKI转换为奥西替尼。结果:奥西替尼的无进展生存期和从开始治疗到进展到奥西替尼的时间在挽救使用和切换使用奥西替尼之间是相当的。结论:由于缺乏通过T790M对患者的选择,切换使用奥西替尼似乎可以提高EGFR激活突变患者的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Switching from first or second generation EGFR-TKI to osimertinib in EGFR mutation-positive NSCLC.

Aim: We evaluated the efficacy of a novel switch protocol for EGFR-TKIs for EGFR mutation-positive NSCLC.

Materials & methods: Clinical records were collected from the patients who had received one of two sequential combination strategies of EGFR-TKIs: Salvage use of osimertinib for T790M-mediated acquired resistance to an prior EGFR-TKI or switch use of osimertinib where an EGFR-TKI was switched to osimertinib before disease progression.

Results: Progression-free survival of osimertinib and time from the start of treatment until progression to osimertinib was comparable between the salvage use and switch use of osimertinib.

Conclusion: Switch use of osimertinib seemed to produce improved efficacy for patients with activating EGFR mutations, because of the lack of patient selection via T790M.

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