Efficacy of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) in targeted therapy of lung squamous cell carcinoma patients with EGFR mutation: a pooled analysis

被引:9
|
作者
Zhuang, Jingqi [1 ]
Yu, Yongfeng [1 ]
Li, Ziming [1 ]
Lu, Shun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Oncol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
efficacy; lung squamous cell carcinoma; epidermal growth factor receptor mutation; tyrosine kinase inhibitors; pooled analysis; PHASE-II TRIAL; CANCER PATIENTS; 1ST-LINE THERAPY; CHINESE PATIENTS; GEFITINIB TREATMENT; JAPANESE PATIENTS; ERLOTINIB; CHEMOTHERAPY; IMPACT; BEVACIZUMAB;
D O I
10.18632/oncotarget.15726
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This pooled analysis aims to evaluate the efficacy of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) in lung squamous cell carcinoma with EGFR mutation. Methods: Advanced stage (IIIB/IV) lung squamous cell carcinoma patients with EGFR mutations treated with EGFR-TKIs were extracted from the publications searched from the databases of EMBASE, Medline (Ovid SP), Web of Science, Cochrane library, PubMed Publisher, ASCO meeting abstract and Google Scholar before August 2016, or identified from the database of Shanghai Chest Hospital from July 2014 to August 2016. Pooled objective response rate, disease control rate and median progression-free survival were accessed directly or by Kaplan-Meier method and combined in different studies by Comprehensive Meta Analysis software via one-group dichotomous or continuous analysis functions. Results: The combined objective response rate, disease control rate and median progression-free survival were 31.6% (95% CI, 24.1%similar to 40.2%), 72.0% (95% CI, 63.5%similar to 79.2%) and 3.08 months (95% CI, 2.31-3.84 months) in lung squamous cell carcinoma patients with EGFR mutation. Conclusion: The EGFR-TKIs had a modest response for EGFR mutated lung squamous cell carcinoma patients and might be a selective option for those patients.
引用
收藏
页码:53675 / 53683
页数:9
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