Tumor-associated macrophages correlate with response to epidermal growth factor receptor-tyrosine kinase inhibitors in advanced non-small cell lung cancer

被引:80
作者
Chung, Fu-Tsai [1 ,2 ,3 ]
Lee, Kang-Yun [1 ,3 ]
Wang, Chih-Wei [4 ]
Heh, Chih-Chen [1 ]
Chan, Yao-Fei [1 ]
Chen, Huan-Wu [5 ]
Kuo, Chih-Hsi [1 ,3 ]
Feng, Po-Hao [1 ,2 ,3 ]
Lin, Ting-Yu [1 ,3 ]
Wang, Chun-Hua [1 ,3 ]
Chou, Chun-Liang [1 ,3 ]
Chen, Hao-Cheng [1 ,3 ]
Lin, Shu-Min [1 ,3 ]
Kuo, Han-Pin [1 ,3 ]
机构
[1] Chang Gung Mem Hosp, Pulm Dis Res Ctr, Linkou, Taiwan
[2] Chang Gung Univ, Grad Inst Clin Med Sci, Coll Med, Tao Yuan, Taiwan
[3] Chang Gung Univ, Dept Internal Med, Chang Gung Mem Hosp Linkou, Coll Med, Taipei, Taiwan
[4] Chang Gung Univ, Dept Pathol, Chang Gung Mem Hosp Linkou, Coll Med, Taipei, Taiwan
[5] Chang Gung Univ, Dept Radiol, Chang Gung Mem Hosp Linkou, Coll Med, Taipei, Taiwan
关键词
TAM; EGFR-TKIs; response; outcome; advanced NSCLC; NF-KAPPA-B; GEFITINIB; MUTATIONS; SURVIVAL; ADENOCARCINOMA; EXPRESSION; ERLOTINIB; EGFR; POLARIZATION; PROGRESSION;
D O I
10.1002/ijc.27403
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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), 2.8722.4; p = 0.0001 and OR, 0.03; 95% CI, 0.0030.31; p = 0.003, respectively] and OS (OR, 2.641; 95% CI, 1.086.5; p = 0.03 and OR, 0.14; 95% CI, 0.030.56; 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.
引用
收藏
页码:E227 / E235
页数:9
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