Tumor‐associated macrophages correlate with response to epidermal growth factor receptor‐tyrosine kinase inhibitors in advanced non‐small cell lung cancer

医学 内科学 表皮生长因子受体 肿瘤科 肺癌 优势比 癌症
作者
Fu‐Tsai Chung,Kang‐Yun Lee,Chih‐Wei Wang,Chih‐Chen Heh,Yao‐Fei Chan,Huan‐Wu Chen,Chih‐Hsi Kuo,Po‐Hao Feng,Ting‐Yu Lin,Chun‐Hua Wang,Chun‐Liang Chou,Hao‐Cheng Chen,Shu‐Min Lin,Han‐Pin Kuo
出处
期刊:International Journal of Cancer [Wiley]
卷期号:131 (3) 被引量:94
标识
DOI:10.1002/ijc.27403
摘要

Our study investigated whether tumor-associated macrophages (TAMs) in advanced non-small cell lung cancer (NSCLC) are related to treatment response to epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) and may be a predictor of survival. Of 206 advanced NSCLC patients treated (first-line) with an EGFR-TKI at the study hospital from 2006 to 2009, 107 with adequate specimens for assessing CD68 immunohistochemistry as a marker of TAMs were assessed. After EGFR-TKI treatment, response was observed in 55 (51%) patients, and the median follow-up period was 13.5 months. Most TAMs were located in the tumor stroma (>95%) and positively costained with the M2 marker CD163. TAM counts were significantly higher in patients with progressive disease than in those without (p < 0.0001), a trend that remained in patients with known EGFR mutation status (n = 59) and those with wild-type EGFR (n = 20). High TAM counts, among other factors (e.g., wild-type EGFR), were significantly related to poor progression-free survival (PFS) and overall survival (OS) (all p < 0.0001 for TAMs). Multivariate Cox analyses showed that high TAM counts and EGFR mutations were both independent factors associated with PFS [odds ratio (OR), 8.0; 95% confidence interval (CI), 2.87-22.4; p = 0.0001 and OR, 0.03; 95% CI, 0.003-0.31; p = 0.003, respectively] and OS (OR, 2.641; 95% CI, 1.08-6.5; p = 0.03 and OR, 0.14; 95% CI, 0.03-0.56; p = 0.006, respectively). TAMs are related to treatment response irrespective of EGFR mutation and can independently predict survival in advanced NSCLC treated with an EGFR-TKI.
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
myLv98完成签到,获得积分10
1秒前
弃医从个啥完成签到,获得积分10
3秒前
高贵觅山完成签到,获得积分10
5秒前
tough_cookie完成签到 ,获得积分10
7秒前
11秒前
李健的小迷弟应助顾卿采纳,获得10
14秒前
疯狂的寒风完成签到,获得积分10
19秒前
大气迎天完成签到,获得积分10
20秒前
开放的乐驹完成签到 ,获得积分10
20秒前
whitepiece完成签到,获得积分10
20秒前
cathyliu完成签到,获得积分10
21秒前
满hui321完成签到 ,获得积分10
21秒前
鹰击长空完成签到,获得积分10
23秒前
24秒前
Jeffery426完成签到,获得积分10
25秒前
科研小白完成签到 ,获得积分10
27秒前
淳于安筠完成签到 ,获得积分10
28秒前
顾卿发布了新的文献求助10
29秒前
yurunxintian完成签到,获得积分10
29秒前
30秒前
SSDlk完成签到,获得积分10
33秒前
36秒前
端庄代荷完成签到 ,获得积分10
42秒前
不爱吃魔芋完成签到 ,获得积分10
42秒前
手术刀完成签到 ,获得积分10
43秒前
Sweet完成签到 ,获得积分10
46秒前
一行白鹭上青天完成签到 ,获得积分10
51秒前
zhangchen123完成签到,获得积分10
55秒前
sll完成签到 ,获得积分10
57秒前
独指蜗牛完成签到 ,获得积分10
59秒前
菘蓝完成签到 ,获得积分10
1分钟前
温暖冬日完成签到,获得积分10
1分钟前
Hello应助科研通管家采纳,获得10
1分钟前
1分钟前
1分钟前
吉祥高趙完成签到 ,获得积分10
1分钟前
muyangsiyuan完成签到,获得积分10
1分钟前
废羊羊完成签到 ,获得积分10
1分钟前
孙朱珠完成签到,获得积分10
1分钟前
含光完成签到,获得积分10
1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
Cronologia da história de Macau 5000
Merrill's Atlas of Radiographic Positioning and Procedures - 3-Volume Set, 16th Edition 2000
晚清天文学译著《谈天》版本考 720
Matrix Methods in Data Mining and Pattern Recognition 510
Calibre SVRF (Standard Verification Rule Format) Manual 2021 500
Interactions of Vowel Quality and Prosody in East Slavic 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 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7086631
求助须知:如何正确求助?哪些是违规求助? 8744454
关于积分的说明 18495055
捐赠科研通 6633293
什么是DOI,文献DOI怎么找? 3134305
关于科研通互助平台的介绍 2239158
邀请新用户注册赠送积分活动 2109051