亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

EGFR-TKI rechallenge in patients with EGFR-mutated non-small-cell lung cancer who progressed after first-line osimertinib treatment: A multicenter retrospective observational study

奥西默替尼 医学 内科学 肿瘤科 肺癌 回顾性队列研究 挽救疗法 毒性 表皮生长因子受体 癌症 化疗 埃罗替尼
作者
Taisuke Araki,Shintaro Kanda,M Obara,Toshihiko Agatsuma,Yumiko Kakizaki,Mineyuki Hama,Hiroshi Yamamoto,Munetake Takada,Manabu Yamamoto,Akemi Matsuo,Daichi Kondo,Masamichi Komatsu,Kei Sonehara,Kazunari Tateishi,Masayuki Hanaoka,Tomonobu Koizumi
出处
期刊:Respiratory investigation [Elsevier BV]
卷期号:62 (2): 262-268 被引量:4
标识
DOI:10.1016/j.resinv.2024.01.002
摘要

Rechallenge therapy with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) is known to confer some clinical benefit for patients with metastatic EGFR-mutated non-small cell lung cancer (NSCLC). However, little is known about the efficacy of EGFR-TKI rechallenge after resistance to first-line (1L) osimertinib. This study aimed to assess the efficacy and safety of EGFR-TKI rechallenge therapy after resistance to 1L osimertinib in a Japanese clinical setting. Between April 2018 and August 2022, 26 patients who progressed after treatment with 1L osimertinib and received EGFR-TKI rechallenge were included in this multicenter retrospective analysis. Patients in whom 1L osimertinib was discontinued owing to toxicity and had subsequent disease progression were also included in the analysis. Overall, the objective response rate for rechallenge therapy was 23.1%. The disease control rate was 53.9%, and the median progression-free survival (PFS) was 3.4 months. Patients who discontinued 1L osimertinib for toxicity had a higher response rate (42.9% vs. 15.8%) and longer PFS than those who discontinued it due to disease progression (median: 11.4 vs. 2.7 months, P = 0.001). Three patients (11.5%) developed rechallenge therapy-associated pneumonitis, two of which were grade ≥3. Rechallenge with EGFR-TKI after 1L osimertinib resistance showed limited clinical efficacy. However, it could be considered as a subsequent salvage therapeutic option for patients in whom 1L osimertinib was discontinued owing to toxicity.
最长约 10秒,即可获得该文献文件

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
张潘完成签到 ,获得积分10
5秒前
李健的小迷弟应助Kevin采纳,获得10
10秒前
17秒前
lyy发布了新的文献求助10
22秒前
mellow完成签到,获得积分10
27秒前
哔哩哔哩哔哔哔完成签到,获得积分10
35秒前
慕青应助哔哩哔哩哔哔哔采纳,获得200
39秒前
41秒前
50秒前
莫提斯完成签到,获得积分20
50秒前
CodeCraft应助星火燎原采纳,获得10
1分钟前
1分钟前
vvan发布了新的文献求助10
1分钟前
星火燎原发布了新的文献求助10
1分钟前
星火燎原完成签到,获得积分10
1分钟前
1分钟前
Mic应助幽默身影采纳,获得30
1分钟前
李爱国应助Brendan采纳,获得10
1分钟前
1分钟前
Yuuuan完成签到,获得积分10
1分钟前
遥感小虫完成签到,获得积分10
2分钟前
遥感小虫发布了新的文献求助30
2分钟前
vvan发布了新的文献求助10
2分钟前
俊秀的梦竹完成签到 ,获得积分10
2分钟前
3分钟前
3分钟前
天天快乐应助HAG采纳,获得10
3分钟前
3分钟前
蜜蜜发布了新的文献求助10
3分钟前
小马甲应助科研通管家采纳,获得10
3分钟前
脑洞疼应助科研通管家采纳,获得10
3分钟前
3分钟前
北欧森林完成签到,获得积分10
3分钟前
HAG发布了新的文献求助10
3分钟前
Yuki完成签到 ,获得积分10
4分钟前
Flicker完成签到 ,获得积分10
4分钟前
4分钟前
谦让蘑菇完成签到,获得积分10
4分钟前
Brendan发布了新的文献求助10
4分钟前
谦让蘑菇发布了新的文献求助20
4分钟前
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
Picture this! Including first nations fiction picture books in school library collections 2000
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1500
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Signals, Systems, and Signal Processing 610
The Oxford Handbook of Archaeology and Language 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6394441
求助须知:如何正确求助?哪些是违规求助? 8209627
关于积分的说明 17382127
捐赠科研通 5447567
什么是DOI,文献DOI怎么找? 2880008
邀请新用户注册赠送积分活动 1856463
关于科研通互助平台的介绍 1699118