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
Jervis完成签到 ,获得积分10
1秒前
1秒前
977完成签到,获得积分10
1秒前
思源应助totpto采纳,获得10
2秒前
行舟完成签到 ,获得积分10
2秒前
林黛玉完成签到 ,获得积分10
3秒前
钱罐罐发布了新的文献求助10
3秒前
完美世界应助儒雅沛蓝采纳,获得10
3秒前
4秒前
CodeCraft应助田村卡夫卡采纳,获得10
6秒前
6秒前
6秒前
852应助不想说采纳,获得10
6秒前
6秒前
6秒前
传奇3应助田村卡夫卡采纳,获得30
6秒前
6秒前
6秒前
pink发布了新的文献求助10
6秒前
7秒前
大个应助钱罐罐采纳,获得10
7秒前
binshier完成签到,获得积分10
7秒前
方愚发布了新的文献求助50
8秒前
zztand发布了新的文献求助10
9秒前
zarahn完成签到,获得积分10
10秒前
11秒前
hongcha完成签到,获得积分10
13秒前
14秒前
Wuzy发布了新的文献求助20
15秒前
儒雅沛蓝发布了新的文献求助10
15秒前
song完成签到 ,获得积分10
16秒前
ada发布了新的文献求助10
17秒前
共享精神应助somous采纳,获得10
18秒前
浅了完成签到,获得积分20
19秒前
20秒前
曾经冰露完成签到,获得积分10
20秒前
科研通AI6.3应助雪糕采纳,获得10
21秒前
22秒前
桐桐应助LH采纳,获得10
24秒前
波比发布了新的文献求助10
25秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
ズームレンズの光学設計に関する研究 800
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 7277194
求助须知:如何正确求助?哪些是违规求助? 8898217
关于积分的说明 18816706
捐赠科研通 6949773
什么是DOI,文献DOI怎么找? 3206458
关于科研通互助平台的介绍 2377437
邀请新用户注册赠送积分活动 2181351