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
老福贵儿应助少卿采纳,获得10
1秒前
矮小的向雪完成签到 ,获得积分10
2秒前
上官若男应助科研通管家采纳,获得10
2秒前
2秒前
上官若男应助科研通管家采纳,获得10
2秒前
李健应助科研通管家采纳,获得10
2秒前
moika完成签到,获得积分10
2秒前
斯文败类应助科研通管家采纳,获得10
2秒前
bkagyin应助科研通管家采纳,获得10
2秒前
2秒前
研友_VZG7GZ应助科研通管家采纳,获得10
2秒前
共享精神应助科研通管家采纳,获得10
2秒前
3秒前
3秒前
zhonglv7应助科研通管家采纳,获得10
3秒前
3秒前
赘婿应助科研通管家采纳,获得10
3秒前
3秒前
wanci应助科研通管家采纳,获得10
3秒前
李爱国应助科研通管家采纳,获得10
3秒前
秋迎夏应助科研通管家采纳,获得10
3秒前
上官若男应助科研通管家采纳,获得10
3秒前
领导范儿应助科研通管家采纳,获得10
3秒前
3秒前
3秒前
动听的时光完成签到,获得积分10
3秒前
adding发布了新的文献求助10
4秒前
月白发布了新的文献求助10
4秒前
传奇3应助丰富的绿茶采纳,获得10
5秒前
小太阳完成签到,获得积分10
5秒前
tongluobing完成签到,获得积分10
5秒前
7秒前
阿来完成签到,获得积分10
7秒前
7秒前
swy完成签到,获得积分10
7秒前
9秒前
研友_8926mL发布了新的文献求助10
9秒前
Lee完成签到,获得积分20
10秒前
small桐发布了新的文献求助20
11秒前
好滴捏发布了新的文献求助10
13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
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Pulse width control of a 3-phase inverter with non sinusoidal phase voltages 777
Signals, Systems, and Signal Processing 610
Research Methods for Applied Linguistics 500
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 6396165
求助须知:如何正确求助?哪些是违规求助? 8211441
关于积分的说明 17393784
捐赠科研通 5449521
什么是DOI,文献DOI怎么找? 2880549
邀请新用户注册赠送积分活动 1857118
关于科研通互助平台的介绍 1699454