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
li完成签到,获得积分10
刚刚
情怀应助呵呵采纳,获得10
1秒前
科研通AI6.2应助皮皮团采纳,获得10
3秒前
Aurora完成签到,获得积分10
5秒前
Hello应助尼古拉斯采纳,获得10
7秒前
10秒前
11秒前
11秒前
活力惜海完成签到,获得积分20
12秒前
香蕉觅云应助huxiaowen采纳,获得10
14秒前
bkagyin应助淡定采纳,获得20
16秒前
XY完成签到,获得积分10
16秒前
Zhang发布了新的文献求助30
16秒前
17秒前
chen发布了新的文献求助10
17秒前
18秒前
科研通AI6.3应助皮皮团采纳,获得10
19秒前
风趣靳完成签到,获得积分10
19秒前
友好的草莓完成签到,获得积分10
19秒前
汉堡包应助babao采纳,获得10
19秒前
尹妮妮发布了新的文献求助10
20秒前
晓晓完成签到,获得积分10
20秒前
lzp完成签到 ,获得积分10
23秒前
23秒前
皮皮团发布了新的文献求助10
24秒前
小小人儿发布了新的文献求助10
24秒前
chen完成签到,获得积分10
25秒前
努力读文献完成签到 ,获得积分10
25秒前
26秒前
大道无形完成签到,获得积分10
28秒前
huxiaowen发布了新的文献求助10
28秒前
29秒前
白糖完成签到,获得积分10
29秒前
29秒前
李健应助Vinent采纳,获得10
31秒前
呵呵发布了新的文献求助10
33秒前
balabala完成签到,获得积分10
33秒前
圣诞节完成签到,获得积分10
33秒前
尹妮妮完成签到,获得积分10
33秒前
科研通AI6.4应助yyy采纳,获得30
34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
Cronologia da história de Macau 5000
Petrology and Plate Tectonics 800
Electrode Potentials 550
Matrix Methods in Data Mining and Pattern Recognition 510
Trees of tropical Asia : an illustrated guide to diversity 500
Materials Informatics Molecules, Crystals and Beyond A volume in Acta Materialia Book Series 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 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 7046799
求助须知:如何正确求助?哪些是违规求助? 8712637
关于积分的说明 18448781
捐赠科研通 6561349
什么是DOI,文献DOI怎么找? 3118699
关于科研通互助平台的介绍 2204833
邀请新用户注册赠送积分活动 2094082