Impact of Smoking Status on EGFR-TKI Efficacy for Advanced Non-Small-Cell Lung Cancer in EGFR Mutants: A Meta-analysis

被引:55
|
作者
Zhang, Yaxiong [1 ,2 ,3 ,4 ]
Kang, Shiyang [1 ,2 ,3 ,4 ]
Fang, Wenfeng [1 ,2 ,3 ]
Hong, Shaodong [1 ,2 ,3 ]
Liang, Wenhua [1 ,2 ,3 ]
Yan, Yue [1 ,2 ,3 ]
Qin, Tao [1 ,2 ,3 ]
Tang, Yanna [1 ,2 ,3 ]
Sheng, Jin [1 ,2 ,3 ]
Zhang, Li [1 ,2 ,3 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, Dept Med Oncol, Guangzhou 510060, Guangdong, Peoples R China
[2] State Key Lab Oncol South China, Guangzhou, Guangdong, Peoples R China
[3] Collaborat Innovat Ctr Canc Med, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Zhongshan Sch Med, Guangzhou 510060, Guangdong, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
EGFR mutation; Meta-analysis; Non-small-cell lung cancer; Smoking; TKI; GROWTH-FACTOR-RECEPTOR; KINASE INHIBITORS; CIGARETTE-SMOKING; EXON; 19; MUTATIONS; ERLOTINIB; GEFITINIB; GENE; ADENOCARCINOMA; RESISTANCE;
D O I
10.1016/j.cllc.2014.09.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We assessed the impact of smoking on response to epidermal growth factor receptor (EGFR) etyrosine kinase inhibitors (TKIs) in advanced non-small-cell lung cancer EGFR-mutant patients incorporating 9 studies that involved 1029 patients. Nonsmokers had longer progression-free survival than ever smokers after EGFR-TKI treatment. Smoking history should be considered an essential factor in studies regarding EGFR-targeted agents toward EGFR mutants. Background: The strong association between smoking history and the presence of epidermal growth factor receptor (EGFR) mutations has been proven in non-small-cell lung cancer (NSCLC), which explains the favorable response to EGFR-tyrosine kinase inhibitor (EGFR-TKI) therapy in nonsmoking NSCLC patients. However, few studies directly focus on the relationship between EGFR-TKI's efficacy and smoking history in NSCLC EGFR-mutant patients. Methods: Electronic databases were searched for eligible literatures. Data on objective response rates, disease control rates, and progression-free survival (PFS) stratified by smoking status were extracted and synthesized on the basis of a random-effect model. Subgroup and sensitivity analyses were conducted. Results: A total of 9 studies that involved a total of 1029 EGFR-mutant advanced NSCLC patients after EGFR-TKI treatment were included. In overall, nonsmoking was associated with significant prolonged PFS (HR, 0.73, 0.60 to 0.88; P = .001) compared to ever smokers. However, only marginal improvements without statistical significance in objective response rates (odds ratio, 1.11; 95% confidence interval, 0.85 to 1.46; P = .433) and disease control rate (odds ratio, 1.04; 95% confidence interval, 0.82 to 1.33; P = .740) were observed. Subgroup analyses showed that the benefits of PFS in nonsmokers were predominantly presented in pooled results of studies enrolling patients with active EGFR mutations, studies involving previously treated patients, and retrospective studies. Additionally, we failed to observe any significant benefit from nonsmokers in every subgroup for objective response rates and disease control rate. Conclusion: For advanced NSCLC patients with EGFR mutations, nonsmoking is associated with longer PFS than ever smoking after EGFR-TKIs treatment. Smoking history should be considered an essential factor in studies regarding EGFR-targeted agents toward EGFR-mutant patients. (C) 2015 The Authors. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:144 / U113
页数:9
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