A randomized Phase 2 study to compare erlotinib with or without bevacizumab in previously untreated patients with advanced non–small cell lung cancer with EGFR mutation

埃罗替尼 贝伐单抗 医学 内科学 盐酸厄洛替尼 肺癌 肿瘤科 危险系数 胃肠病学 表皮生长因子受体 癌症 化疗 置信区间
作者
Youngjoo Lee,Hye Ryun Kim,Min Hee Hong,Ki Hyeong Lee,Keon Uk Park,Geon Kook Lee,Hyae Young Kim,Soo-Hyun Lee,Key Hwan Lim,Sung Jin Yoon,Byoung Chul Cho,Ji‐Youn Han
出处
期刊:Cancer [Wiley]
卷期号:129 (3): 405-414 被引量:4
标识
DOI:10.1002/cncr.34553
摘要

This study evaluated whether an addition of bevacizumab to erlotinib improves clinical outcomes in patients with advanced EGFR-mutated non-small cell lung cancer (NSCLC).This is an open-label, multicenter, randomized Phase 2 study in South Korea. Chemonaïve patients with Stage IIIB/IV NSCLC with EGFR 19 deletion or L858R mutation were eligible. Asymptomatic brain metastasis (BM) was enrolled without local treatment. Patients received either erlotinib plus bevacizumab or erlotinib.Between December 2016 and March 2019, 127 patients were randomly assigned to receive erlotinib plus bevacizumab (n = 64) or erlotinib (n = 63). Fifty-nine (46.5%) patients had baseline BM. Fewer patients in the erlotinib plus bevacizumab arm received radiotherapy for BM than in the erlotinib arm (10.3% vs. 40.0%). A trend toward longer progression-free survival (PFS) was observed in the erlotinib plus bevacizumab arm compared with the erlotinib alone arm; however, it was not statistically significant (median PFS, 17.5 months vs. 12.4 months; hazard ratio [HR], 0.74; 95% CI, 0.51-1.08; p = .119). The unplanned subgroup analysis showed a longer PFS with erlotinib plus bevacizumab in patients with BM (median PFS, 18.6 months vs. 10.3 months; HR, 0.54; 95% CI, 0.31-0.95; p = .032). Grade 3 or worse adverse events occurred in 56.6% of the erlotinib plus bevacizumab arm and 20.6% of the erlotinib arm.Although it was not statistically significant, a trend to improvement in PFS was observed in patients with erlotinib plus bevacizumab compared to erlotinib alone.A randomized Phase 2 study compared erlotinib with or without bevacizumab in previously untreated patients with advanced non-small cell lung cancer with EGFR mutation. The erlotinib plus bevacizumab failed to improve median progression-free survival compared with the erlotinib alone. However, the progression-free survival benefit from erlotinib plus bevacizumab was found in patients with brain metastasis with no severe hemorrhagic adverse effects.
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
Derek完成签到,获得积分0
刚刚
onw完成签到,获得积分10
1秒前
爱岗敬业牛马人完成签到 ,获得积分10
3秒前
Herman完成签到 ,获得积分10
5秒前
BBA完成签到 ,获得积分10
5秒前
channing完成签到,获得积分20
6秒前
沉淀完成签到 ,获得积分10
8秒前
华仔应助celine采纳,获得10
12秒前
yefeng完成签到,获得积分10
12秒前
冯梦梦完成签到 ,获得积分10
18秒前
Xpaper完成签到,获得积分10
24秒前
科研通AI5应助科研通管家采纳,获得30
26秒前
鹿璐发布了新的文献求助10
26秒前
26秒前
科研通AI2S应助科研通管家采纳,获得10
26秒前
cavendipeng完成签到,获得积分10
26秒前
科研通AI5应助科研通管家采纳,获得10
26秒前
爆米花应助科研通管家采纳,获得30
26秒前
打打应助科研通管家采纳,获得10
26秒前
科研通AI5应助科研通管家采纳,获得10
26秒前
26秒前
地学韦丰吉司长完成签到,获得积分10
28秒前
Bizibili完成签到,获得积分10
30秒前
完美世界应助婷婷大侠采纳,获得10
30秒前
重要的哈密瓜完成签到 ,获得积分10
30秒前
坦率雁卉完成签到,获得积分10
30秒前
Ahha完成签到 ,获得积分10
31秒前
车宇完成签到 ,获得积分10
32秒前
李健应助Orchid采纳,获得10
36秒前
小兔子完成签到,获得积分10
38秒前
Lorain完成签到,获得积分20
38秒前
岂有此李完成签到,获得积分10
43秒前
绿波电龙完成签到,获得积分10
45秒前
可爱的香菇完成签到 ,获得积分10
45秒前
47秒前
xiaoxiao完成签到,获得积分10
47秒前
选课完成签到,获得积分10
47秒前
安静依琴完成签到,获得积分10
48秒前
婷婷大侠发布了新的文献求助10
54秒前
唐禹嘉完成签到 ,获得积分10
55秒前
高分求助中
Introduction to Strong Mixing Conditions Volumes 1-3 500
Tip60 complex regulates eggshell formation and oviposition in the white-backed planthopper, providing effective targets for pest control 400
Optical and electric properties of monocrystalline synthetic diamond irradiated by neutrons 320
共融服務學習指南 300
Essentials of Pharmacoeconomics: Health Economics and Outcomes Research 3rd Edition. by Karen Rascati 300
Peking Blues // Liao San 300
Political Ideologies Their Origins and Impact 13 edition 240
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 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3801092
求助须知:如何正确求助?哪些是违规求助? 3346581
关于积分的说明 10329787
捐赠科研通 3063102
什么是DOI,文献DOI怎么找? 1681341
邀请新用户注册赠送积分活动 807491
科研通“疑难数据库(出版商)”最低求助积分说明 763726