The comparisons of the efficacy and toxicity between gefitinib and docetaxel for patients with advanced nonsmall-cell lung cancer: A meta-analysis from randomized controlled clinical trials

被引:1
|
作者
Zhao, Y. L. [1 ]
Han, S. [2 ,3 ]
Pu, R. [4 ]
Shi, L. W. [1 ,3 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
[2] Peking Univ, Sch Publ Hlth, Beijing 100191, Peoples R China
[3] Peking Univ, Int Res Ctr Med Adm, Beijing 100191, Peoples R China
[4] China Natl Ctr Biotechnol Dev, Beijing 100039, Peoples R China
关键词
Docetaxel; gefitinib; meta-analysis; NSCLC; PHASE-III TRIAL; PLATINUM-BASED CHEMOTHERAPY; PERFORMANCE STATUS; MUTATIONS; MORTALITY; THERAPY; QUALITY; CHINA;
D O I
10.4103/0019-509X.154070
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The extent of the benefit of gefitinib in the treatment of advanced nonsmall-cell lung cancer (NSCLC) is till controversial, when compared with docetaxel. We performed this meta-analysis to compare the efficacy and toxicity of gefitinib with docetaxel for different patients with advanced NSCLC. Materials and Methods: We searched PubMed, Cochrane Library, and identified 5 randomized controlled clinical trials published within 2000-2013. After further full-text screening, 4 clinical trials were included in the final meta-analysis. Results: The outcomes of treatment efficacy included progression-free survival (PFS), overall survival (OS) and objective response rate (ORR). Comparing gefitinib to docetaxel for advanced NSCLC patients, the pooled hazard ratio (HR) of PFS was 0.91, (95% confidential index [CI] = 0.83-0.99), the pooled HR of OS was 1.02, (95% CI = 0.93-1.13), the pooled risk ratio of ORR was 1.57, (95% CI = 1.01-2.47). Conclusions: Gefitinib was found to significantly improve patients PFS and response rate compared with docetaxel. There is no difference of OS between gefitinib and docetaxel.
引用
收藏
页码:86 / 91
页数:6
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