Afatinib Versus Osimertinib as First-Line Treatment for Advanced EGFR-Mutant Non-Small-Cell Lung Cancer: A 3-Year Follow-Up Overall Survival Analysis.

IF 5.1 3区 医学 Q2 ONCOLOGY
Targeted Oncology Pub Date : 2026-07-01 Epub Date: 2026-06-08 DOI:10.1007/s11523-026-01224-1
Yen-Hsiang Huang, Kuo-Hsuan Hsu, Jeng-Sen Tseng, Po-Hsin Lee, I-Hung Lin, Mu-Han Peng, Tsung-Ying Yang
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引用次数: 0

Abstract

Background: To date, there are limited clinical trials comparing the clinical efficacy between second-generation and third-generation epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKI)s.

Objective: The objective of this study was to compare the survival outcomes between afatinib and osimertinib as first-line treatments in patients with advanced EGFR-mutant non-small-cell lung cancer (NSCLC).

Patients and methods: Between January 2018 and December 2020, we retrospectively enrolled patients with advanced NSCLC harboring an exon 19 deletion or L858R mutation who received afatinib or osimertinib as first-line treatment to analyze the progression-free survival (PFS) and overall survival (OS).

Results: A total of 128 patients were included in this study, with 81 in the afatinib group and 47 in the osimertinib group. The median follow-up time was 39.9 months for the afatinib group and 37.0 months for the osimertinib group. The median PFS was 13.5 months in the afatinib group and 18.2 months in the osimertinib group (p = 0.240). The median OS was 40.5 months in the afatinib group and 37.0 months in the osimertinib group (p = 0.980). A total of 63% of patients received osimertinib as sequential therapy following progression on afatinib, with a median OS of 41.7 months. Among these patients, the median OS was 41.7 months for those with a detected T790M mutation, 42.0 months for those without the mutation, and 35.6 months for those with unknown T790M mutation status.

Conclusions: Our study demonstrated that both afatinib and osimertinib as first-line treatments offer favorable median OS in patients with advanced EGFR-mutant NSCLC. In addition, we recommend that patients receiving afatinib as first-line therapy undergo sequential osimertinib treatment, regardless of their T790M mutation status.

阿法替尼与奥西替尼作为晚期egfr突变非小细胞肺癌的一线治疗:3年随访总生存分析
背景:迄今为止,比较第二代和第三代表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKI)临床疗效的临床试验有限。目的:本研究的目的是比较阿法替尼和奥西替尼作为一线治疗晚期egfr突变的非小细胞肺癌(NSCLC)患者的生存结果。患者和方法:在2018年1月至2020年12月期间,我们回顾性招募了携带外显子19缺失或L858R突变的晚期NSCLC患者,这些患者接受了阿法替尼或奥西替尼作为一线治疗,以分析无进展生存期(PFS)和总生存期(OS)。结果:本研究共纳入128例患者,其中阿法替尼组81例,奥西替尼组47例。阿法替尼组中位随访时间为39.9个月,奥西替尼组中位随访时间为37.0个月。阿法替尼组的中位PFS为13.5个月,奥西替尼组为18.2个月(p = 0.240)。阿法替尼组的中位OS为40.5个月,奥希替尼组的中位OS为37.0个月(p = 0.980)。共有63%的患者在阿法替尼进展后接受了奥西替尼作为序贯治疗,中位OS为41.7个月。在这些患者中,检测到T790M突变的患者中位生存期为41.7个月,未检测到T790M突变的患者中位生存期为42.0个月,T790M突变状态未知的患者中位生存期为35.6个月。结论:我们的研究表明,阿法替尼和奥西替尼作为一线治疗对于晚期egfr突变的NSCLC患者具有良好的中位OS。此外,我们建议接受阿法替尼作为一线治疗的患者接受序贯奥西替尼治疗,无论其T790M突变状态如何。
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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来源期刊
Targeted Oncology
Targeted Oncology 医学-肿瘤学
CiteScore
8.40
自引率
3.70%
发文量
64
审稿时长
>12 weeks
期刊介绍: Targeted Oncology addresses physicians and scientists committed to oncology and cancer research by providing a programme of articles on molecularly targeted pharmacotherapy in oncology. The journal includes: Original Research Articles on all aspects of molecularly targeted agents for the treatment of cancer, including immune checkpoint inhibitors and related approaches. Comprehensive narrative Review Articles and shorter Leading Articles discussing relevant clinically established as well as emerging agents and pathways. Current Opinion articles that place interesting areas in perspective. Therapy in Practice articles that provide a guide to the optimum management of a condition and highlight practical, clinically relevant considerations and recommendations. Systematic Reviews that use explicit, systematic methods as outlined by the PRISMA statement. Adis Drug Reviews of the properties and place in therapy of both newer and established targeted drugs in oncology.
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