亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

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
yubaobao完成签到,获得积分10
1秒前
pjy完成签到 ,获得积分10
3秒前
yeah完成签到,获得积分10
8秒前
渭阳野士完成签到,获得积分10
11秒前
脑洞疼应助科研通管家采纳,获得10
12秒前
12秒前
FashionBoy应助科研通管家采纳,获得10
13秒前
wanci应助科研通管家采纳,获得10
13秒前
上官若男应助科研通管家采纳,获得10
13秒前
SciGPT应助科研通管家采纳,获得10
14秒前
14秒前
呆萌糖豆发布了新的文献求助10
21秒前
韩祖完成签到 ,获得积分10
27秒前
27秒前
斯文败类应助忐忑的黄豆采纳,获得10
34秒前
专一的绮露完成签到,获得积分20
34秒前
Xiaowen发布了新的文献求助10
34秒前
35秒前
43秒前
无花果应助Xiaowen采纳,获得10
45秒前
48秒前
小马甲应助盲点采纳,获得10
49秒前
27完成签到 ,获得积分10
1分钟前
iShine完成签到 ,获得积分10
1分钟前
1分钟前
科研通AI6.2应助李小伟采纳,获得10
1分钟前
1分钟前
搜集达人应助梅子酒采纳,获得10
1分钟前
张不大完成签到,获得积分10
1分钟前
1分钟前
wjy完成签到 ,获得积分10
1分钟前
一杯茶具完成签到 ,获得积分10
1分钟前
1分钟前
1分钟前
李小伟发布了新的文献求助10
1分钟前
梅子酒发布了新的文献求助10
1分钟前
lingzi发布了新的文献求助10
1分钟前
haichun完成签到 ,获得积分10
1分钟前
lingzi完成签到,获得积分20
1分钟前
1分钟前
高分求助中
Ideology and Meaning-Making under the Putin Regime 750
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
Handbook of Luminescence Dating 500
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
Introduction to Industrial/Organizational Psychology 400
Advances in Design and Control Robust Adaptive Control: Deadzone-Adapted Disturbance Suppression 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 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6927112
求助须知:如何正确求助?哪些是违规求助? 8615645
关于积分的说明 18276733
捐赠科研通 6347542
什么是DOI,文献DOI怎么找? 3072251
关于科研通互助平台的介绍 2105503
邀请新用户注册赠送积分活动 2049367