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
初景发布了新的文献求助10
刚刚
失眠的冬易完成签到 ,获得积分10
1秒前
含光完成签到,获得积分10
8秒前
Kashing完成签到,获得积分10
10秒前
lydiaabc完成签到,获得积分10
13秒前
专注香芦完成签到 ,获得积分10
14秒前
kevinrnk完成签到,获得积分10
16秒前
脑洞疼应助科研通管家采纳,获得10
24秒前
丘比特应助科研通管家采纳,获得10
24秒前
wanci应助科研通管家采纳,获得10
24秒前
FashionBoy应助科研通管家采纳,获得10
24秒前
打打应助科研通管家采纳,获得10
24秒前
小猫完成签到 ,获得积分10
25秒前
周俊瑞完成签到 ,获得积分10
26秒前
hxy完成签到 ,获得积分10
27秒前
tough_cookie完成签到 ,获得积分10
29秒前
asdwind完成签到,获得积分10
31秒前
freebird完成签到,获得积分10
33秒前
安风完成签到 ,获得积分10
39秒前
Vigour完成签到 ,获得积分10
40秒前
笨笨千亦完成签到 ,获得积分10
41秒前
千夜冰柠萌完成签到,获得积分10
42秒前
852应助海豚采纳,获得10
46秒前
炎炎夏无声完成签到 ,获得积分10
47秒前
chemistry高完成签到 ,获得积分10
48秒前
50秒前
一行白鹭上青天完成签到 ,获得积分10
50秒前
自转无风完成签到,获得积分10
51秒前
魔术师完成签到 ,获得积分10
51秒前
Flowing完成签到,获得积分10
54秒前
57秒前
风中星月完成签到 ,获得积分10
58秒前
想发一篇贾克斯完成签到,获得积分10
1分钟前
聂先生完成签到,获得积分10
1分钟前
Yuki完成签到 ,获得积分10
1分钟前
XU博士完成签到,获得积分10
1分钟前
今后应助沉默安波采纳,获得10
1分钟前
aaaa完成签到,获得积分10
1分钟前
无奈山雁完成签到 ,获得积分10
1分钟前
三脸茫然完成签到 ,获得积分0
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
Developing Genetic Editing Tools for Lysobacter 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
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 6523260
求助须知:如何正确求助?哪些是违规求助? 8316260
关于积分的说明 17793806
捐赠科研通 5625232
什么是DOI,文献DOI怎么找? 2928180
邀请新用户注册赠送积分活动 1904876
关于科研通互助平台的介绍 1765054