Dacomitinib overcomes acquired resistance to osimertinib in advanced NSCLC patients with EGFR L718Q mutation: A two-case report

奥西默替尼 医学 T790米 吉非替尼 肿瘤科 腺癌 内科学 肺癌 背景(考古学) 表皮生长因子受体 癌症 生物 古生物学 ROS1型
作者
J. li,Meizi Jin,Yuzhu Diao,Li Xiaoling
出处
期刊:Medicine [Ovid Technologies (Wolters Kluwer)]
卷期号:103 (28): e38789-e38789 被引量:1
标识
DOI:10.1097/md.0000000000038789
摘要

Rationale: Acquired resistance still inevitably occurs in patients treated with third-generation TKI osimertinib. Although the EGFR L718Q mutation has been reported as a scarce mechanism of osimertinib resistance, advanced therapeutic strategies are still in development. In this report, we included 2 cases of patients who acquired EGFR L858R/L718Q mutation after osimertinib and were overcome by dacomitinib. Patient concerns: Case 1: A 77-year-old woman was diagnosed with stage IV lung adenocarcinoma. Case 2: A 64-year-old woman was diagnosed with stage IV lung adenocarcinoma. Diagnoses: Case 1: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Since then, treatment with gefitinib was administrated, leading to a progression-free survival of 18 months. The treatment was switched to osimertinib based on the detection of EGFR T790M mutation, resulting in a progression-free survival of 24 months. Subsequently, EGFR L718Q mutation was detected. Case 2: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Icotinib was used as the first-line treatment for 7 months. Osimertinib was applied as the second-line treatment for 13 months based on the EGFR T790M mutation. Subsequently, EGFR L718Q mutation was detected. Interventions: Case 1: Dacomitinib was administered. Case 2: Dacomitinib was administered. Outcomes: Case 1:The progression-free survival was 8 months. Case 2: The progression-free survival was 3 months. Lessons: Dacomitinib is a potential treatment option for NSCLC patients with EGFR L718Q mutation after resistance to Osimertinib. Further research is needed to validate the efficacy of Dacomitinib in this context.

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
刚刚
safari完成签到 ,获得积分10
刚刚
yingzaifeixiang完成签到 ,获得积分10
1秒前
2秒前
自然冥幽完成签到,获得积分10
2秒前
披着羊皮的狼完成签到,获得积分0
3秒前
球球完成签到,获得积分10
3秒前
楚楚完成签到 ,获得积分10
4秒前
初见完成签到 ,获得积分10
4秒前
禾禾禾完成签到,获得积分10
4秒前
秘书完成签到 ,获得积分10
6秒前
小五完成签到 ,获得积分10
6秒前
7秒前
熊雅完成签到,获得积分10
8秒前
10秒前
kyt完成签到 ,获得积分10
10秒前
争当科研巨匠完成签到,获得积分10
11秒前
12秒前
尹冰露完成签到,获得积分10
13秒前
安静严青完成签到 ,获得积分10
15秒前
热心市民小杨应助云山采纳,获得10
15秒前
ice完成签到 ,获得积分10
16秒前
饱满芷卉完成签到,获得积分10
16秒前
子苓完成签到 ,获得积分10
16秒前
左西完成签到 ,获得积分10
16秒前
哎呀完成签到,获得积分10
16秒前
lalala发布了新的文献求助10
17秒前
起风了完成签到 ,获得积分10
19秒前
jixuchance完成签到,获得积分10
19秒前
长情琦完成签到,获得积分10
19秒前
斯奈克完成签到,获得积分10
19秒前
步步高完成签到,获得积分10
20秒前
20秒前
Ray完成签到 ,获得积分10
20秒前
感性的俊驰完成签到 ,获得积分10
22秒前
23秒前
byby完成签到,获得积分10
24秒前
26秒前
西宁完成签到,获得积分10
26秒前
PDIF-CN2完成签到,获得积分10
27秒前
高分求助中
Modern Epidemiology, Fourth Edition 5000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
Digital Twins of Advanced Materials Processing 2000
Propeller Design 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
First commercial application of ELCRES™ HTV150A film in Nichicon capacitors for AC-DC inverters: SABIC at PCIM Europe 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 化学工程 生物化学 物理 计算机科学 内科学 复合材料 催化作用 物理化学 光电子学 电极 冶金 细胞生物学 基因
热门帖子
关注 科研通微信公众号,转发送积分 6005013
求助须知:如何正确求助?哪些是违规求助? 7526596
关于积分的说明 16112259
捐赠科研通 5150496
什么是DOI,文献DOI怎么找? 2759785
邀请新用户注册赠送积分活动 1736819
关于科研通互助平台的介绍 1632124