Divergent epidermal growth factor receptor mutation patterns between smokers and non-smokers with lung adenocarcinoma

被引:10
|
作者
Tseng, Jeng-Sen [1 ]
Wang, Chih-Liang [2 ,3 ]
Yang, Tsung-Ying [1 ,4 ]
Chen, Chih-Yi [5 ]
Yang, Cheng-Ta [2 ,6 ]
Chen, Kun-Chieh [1 ,7 ]
Hsu, Kuo-Hsuan [7 ,8 ]
Tsai, Chi-Ren [9 ,10 ]
Chang, Gee-Chen [1 ,4 ]
机构
[1] Taichung Vet Gen Hosp, Dept Internal Med, Div Chest Med, Taichung 407, Taiwan
[2] Chang Gung Mem Hosp, Dept Thorac Med, Taoyuan 333, Taiwan
[3] Chang Gung Univ, Coll Med, Taoyuan 333, Taiwan
[4] Natl Yang Ming Univ, Sch Med, Fac Med, Taipei 112, Taiwan
[5] Chung Shan Med Univ, Chung Shan Med Univ Hosp, Dept Surg, Inst Med,Div Thorac Surg, Taichung 402, Taiwan
[6] Chang Gung Univ, Coll Med, Dept Resp Therapy, Taoyuan 333, Taiwan
[7] Natl Chung Hsing Univ, Inst Biomed Sci, Taichung 402, Taiwan
[8] Taichung Vet Gen Hosp, Dept Internal Med, Div Crit Care & Resp Therapy, Taichung 407, Taiwan
[9] Taichung Vet Gen Hosp, Dept Pediat, Taichung 407, Taiwan
[10] Natl Chung Hsing Univ, Inst Mol Biol, Taichung 402, Taiwan
关键词
Lung cancer; Non-small cell lung cancer (NSCLC); Lung adenocarcinoma; Epidermal growth factor receptor (EGFR) mutation; TYROSINE KINASE INHIBITORS; EXON; 19; DELETIONS; 1ST-LINE TREATMENT; SMOKING STATUS; NEVER SMOKERS; OPEN-LABEL; EGFR; CANCER; CHEMOTHERAPY; GENE;
D O I
10.1016/j.lungcan.2015.09.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Smoking status is an important determinant of the prevalence of epidermal growth factor receptor (EGFR) mutations in lung cancer patients. However, it is unclear whether smoking status could also influence the spectrum of EGFR mutations. Methods: We enrolled patients with lung adenocarcinoma from three medical centers in Taiwan. EGFR mutations were assessed by Sanger direct sequencing. The objective of this study was to evaluate the influence of smoking status on both the frequency and patterns of EGFR mutations. Results: From 2001 to 2013, a total of 1175 patients with lung adenocarcinoma were enrolled for EGFR mutation analysis. The overall EGFR mutation rate was 59.6%, which was significantly higher in females than males (69.1% vs. 49.8%) and in non-smokers than current/former smokers (73.8% vs. 29.8%) (both P< 0.001). Among patients harboring EGFR mutations, smokers expressed L858R mutation less frequently (35.2% vs. 50.2%, P= 0.005) and exon 19 deletions more frequently (52.8% vs 38.8%, P= 0.008) than nonsmokers. Smokers and non-smokers also had divergent exon 19 deletions subtypes (Del E746-A750 82.5% vs. 57.6%, respectively, P< 0.001). Among subgroup patients harboring the L858R mutation, smokers were associated with a higher rate of complex mutations than non-smokers (34.2% vs. 8.4%, P< 0.001). Conclusions: Our results suggested that smoking status could influence not only the frequency but also the spectrum of EGFR mutations. These findings provide a clue for further investigation of EGFR mutagenesis. (c) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:472 / 476
页数:5
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