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
1秒前
RS6完成签到,获得积分10
1秒前
罗豪杰完成签到,获得积分10
1秒前
2秒前
2秒前
3秒前
4秒前
小电驴完成签到,获得积分10
5秒前
自然代亦完成签到 ,获得积分10
7秒前
程破茧完成签到,获得积分10
7秒前
rio发布了新的文献求助10
7秒前
8秒前
研友_564485完成签到,获得积分10
8秒前
ycd发布了新的文献求助10
8秒前
半山完成签到,获得积分10
8秒前
9秒前
9秒前
赫幼蓉发布了新的文献求助10
9秒前
9秒前
9秒前
9秒前
9秒前
9秒前
10秒前
10秒前
10秒前
10秒前
10秒前
10秒前
10秒前
10秒前
10秒前
11秒前
11秒前
11秒前
11秒前
11秒前
11秒前
11秒前
11秒前
高分求助中
The Graphene Handbook (2019 Edition) 800
IEST-RP-CC018: Cleanroom Cleaning and Sanitization: Operating and Monitoring Procedures 600
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
久松真一著作集〈第5巻〉禅と芸術 500
Fundamentals of Modern Mathematics: A Practical Review (Dover Books on Mathematics) 500
Cold War Transcended: Australia's China Policy, 1949-1990 470
Comprehensive Organic Synthesis 400
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 6596760
求助须知:如何正确求助?哪些是违规求助? 8366692
关于积分的说明 17909502
捐赠科研通 5749431
什么是DOI,文献DOI怎么找? 2953182
邀请新用户注册赠送积分活动 1928477
关于科研通互助平台的介绍 1822329