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
小小马发布了新的文献求助10
刚刚
我是老大应助JiangZhi采纳,获得10
刚刚
hhh完成签到 ,获得积分10
1秒前
哭泣天抒发布了新的文献求助10
2秒前
ddd关闭了ddd文献求助
3秒前
3秒前
重要的炳完成签到 ,获得积分10
4秒前
虾虾发布了新的文献求助10
4秒前
发发完成签到,获得积分10
5秒前
菲12345678发布了新的文献求助10
6秒前
7秒前
陈小子完成签到 ,获得积分10
7秒前
回忆发布了新的文献求助10
8秒前
8秒前
8秒前
9秒前
silence完成签到,获得积分10
9秒前
文艺语蓉完成签到,获得积分10
10秒前
畅快的荟完成签到,获得积分10
10秒前
小小马完成签到,获得积分10
11秒前
追梦人完成签到 ,获得积分10
11秒前
不知道发布了新的文献求助10
11秒前
large-ass发布了新的文献求助10
13秒前
13秒前
zzzrrr发布了新的文献求助10
13秒前
14秒前
14秒前
英姑应助哭泣天抒采纳,获得10
17秒前
Arise完成签到,获得积分10
18秒前
隐形曼青应助haha采纳,获得10
19秒前
Ava应助ni采纳,获得10
19秒前
大模型应助菲12345678采纳,获得10
21秒前
21秒前
26秒前
桐桐应助王越采纳,获得10
27秒前
酷波er应助无情干饭崽采纳,获得10
28秒前
科研通AI6.2应助伊倾采纳,获得30
28秒前
Ava应助明理乞采纳,获得10
28秒前
29秒前
手可摘星辰完成签到,获得积分10
30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
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
ON THE THEORY OF BIRATIONAL BLOWING-UP 666
Signals, Systems, and Signal Processing 610
Chemistry and Physics of Carbon Volume 15 500
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 6388684
求助须知:如何正确求助?哪些是违规求助? 8203020
关于积分的说明 17356848
捐赠科研通 5442239
什么是DOI,文献DOI怎么找? 2877912
邀请新用户注册赠送积分活动 1854294
关于科研通互助平台的介绍 1697825