Survival benefits from afatinib compared with gefitinib and erlotinib among patients with common EGFR mutation in first‐line setting

作者
Wang Chun Kwok,Jcm Ho,Terence Chi Chun Tam,Msm Ip,David Chi Leung Lam
出处
期刊:Thoracic Cancer [Wiley]
卷期号:13 (14): 2057-2063 被引量:5
标识
DOI:10.1111/1759-7714.14528
摘要

BACKGROUND: Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) are recommended as first-line treatment in non-small cell lung cancer (NSCLC) patients with sensitizing EGFR mutations. The sequential use of different EGFR-TKIs has been reported to demonstrate improvement in overall survival of NSCLC patients with EGFR mutations. There are limited reports on comparisons between regimens with first-line use of afatinib, gefitinib or erlotinib, followed by osimertinib upon disease progression with acquired T790M mutation. METHODS: A retrospective cohort study of Chinese patients with metastatic NSCLC harboring EGFR mutations who received first-line gefitinib, erlotinib or afatinib treatment, followed by osimertinib upon disease progression with acquired T790M mutation, was conducted. The differences in overall survival (OS) and progression-free survival (PFS) with first-line EGFR-TKI (PFS1) and time to second objective disease progression (PFS2) were compared among patients on different first-line EGFR-TKIs. RESULTS: Among 155 patients, 101 (65.2%), 38 (24.5%) and 16 (10.3%) patients were on first-line gefitinib, erlotinib or afatinib, respectively. Patients treated with afatinib in the first-line setting had significantly longer OS compared with those on gefitinib or erlotinib, while the PFS1 and PFS2 were longer for patients on afatinib but did not reach statistical significance. CONCLUSIONS: First-line afatinib, followed by osimertinib upon disease progression with T790M mutation, demonstrated significantly longer OS compared to that using other EGFR-TKI in the first-line setting.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
星1完成签到 ,获得积分10
1秒前
谨慎铃铛完成签到,获得积分10
2秒前
2秒前
2秒前
czq完成签到,获得积分10
2秒前
2秒前
2秒前
3秒前
3秒前
3秒前
3秒前
吴苏伦发布了新的文献求助10
4秒前
4秒前
昏睡的鱼完成签到,获得积分10
4秒前
4秒前
duoduozs完成签到,获得积分10
4秒前
gkfenomeno发布了新的文献求助30
5秒前
5秒前
5秒前
bkagyin应助SCI采纳,获得10
5秒前
bkagyin应助lululiya采纳,获得10
5秒前
6秒前
6秒前
6秒前
6秒前
6秒前
6秒前
6秒前
6秒前
玛璃鸶完成签到,获得积分10
6秒前
6秒前
7秒前
哇samm完成签到,获得积分10
7秒前
Ado完成签到,获得积分10
7秒前
7秒前
852应助甜蜜的大象采纳,获得10
7秒前
复杂的含蕾完成签到 ,获得积分10
7秒前
7秒前
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Rosenblum, Global Change Biology 500
CLSI VET01S-2024 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals (7th Ed) 500
DIPPR Project 801 - Full Version 380
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7767246
求助须知:如何正确求助?哪些是违规求助? 9310945
关于积分的说明 20320272
捐赠科研通 7352189
什么是DOI,文献DOI怎么找? 3315235
关于科研通互助平台的介绍 2464651
邀请新用户注册赠送积分活动 2329924