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一代 EGFR-TKI 治疗失败的既往治疗的非小细胞肺癌患者中埃非替尼的再挑战。

Re-challenge of afatinib after 1st generation EGFR-TKI failure in patients with previously treated non-small cell lung cancer harboring EGFR mutation.

机构信息

Department of Respiratory Medicine Comprehensive Cancer Center, International Medical Center, Saitama Medical University, 1397-1 Yamane, Hidaka-City, Saitama, 350-1298, Japan.

出版信息

Cancer Chemother Pharmacol. 2019 May;83(5):817-825. doi: 10.1007/s00280-019-03790-w. Epub 2019 Feb 13.

Abstract

BACKGROUND

Re-challenge of erlotinib after gefitinib failure is reported to yield some benefit in patients with non-small cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) mutation. However, little is known about the re-challenge of afatinib after 1st generate on EGFR tyrosine kinase inhibitor (TKI) failure.

METHODS

From May 2015 to August 2018, 62 patients with advanced NSCLC harboring sensitive EGFR mutation received afatinib after gefitinib and/or erlotinib failure at our institution was included in our retrospective study.

RESULTS

The overall response rate (ORR) and disease control rate (DCR) of afatinib as re-challenge were 17.0% and 79.2%, respectively. The median time on treatment of 1st generation EGFR-TKI (1st TKI) was 14 months. By multivariate analysis, smoking, performance status (PS), and time on treatment of 1st TKI with more than 10 months were confirmed to be independent prognostic factors predicting a worse progression-free survival (PFS), and significant prognostic markers for overall survival (OS) were PS and time on treatment of 1st TKI with more than 10 months, especially in patients with exon 19 deletion.

CONCLUSIONS

Re-challenge of afatinib was identified as one of the therapeutic options after 1st TKI failure in the patients with advanced NSCLC harboring EGFR mutation when the time of treatment by prior 1st TKI is more than 10 months.

摘要

背景

表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者在吉非替尼和/或厄洛替尼失败后重新使用厄洛替尼,据报道会产生一定的获益。然而,对于第一代 EGFR 酪氨酸激酶抑制剂(TKI)失败后重新使用阿法替尼知之甚少。

方法

本回顾性研究纳入了 2015 年 5 月至 2018 年 8 月在我院因吉非替尼和/或厄洛替尼治疗失败后接受阿法替尼治疗的 62 例晚期 NSCLC 患者,这些患者均携带敏感 EGFR 突变。

结果

阿法替尼作为二线治疗的总体缓解率(ORR)和疾病控制率(DCR)分别为 17.0%和 79.2%。第一代 EGFR-TKI(1 代 TKI)的中位治疗时间为 14 个月。多因素分析证实,吸烟、体能状态(PS)和 1 代 TKI 治疗时间超过 10 个月是无进展生存期(PFS)不良的独立预后因素,PS 和 1 代 TKI 治疗时间超过 10 个月是总生存期(OS)的显著预后标志物,特别是在存在外显子 19 缺失的患者中。

结论

对于 EGFR 突变的晚期 NSCLC 患者,在 1 代 TKI 治疗时间超过 10 个月时,阿法替尼作为 1 代 TKI 失败后的治疗选择之一。

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