A meta-analysis of erlotinib versus docetaxel for advanced nonsmall-cell lung cancer with poor prognosis

被引:1
|
作者
Xu, W. [1 ]
Jin, C. [1 ]
Dai, X. [2 ]
Lv, X. [3 ]
机构
[1] Sanmen Hosp Tradit Chinese Med, Dept Gen Surg, Sanmen 317100, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Qual Management Off, Hangzhou 310009, Zhejiang, Peoples R China
[3] Zhejiang Univ, Affiliated Hosp 1, Dept Thorac Surg, Hangzhou 310009, Zhejiang, Peoples R China
关键词
Docetaxel; erlotinib; meta-analysis; nonsmall-cell lung cancer; RANDOMIZED CLINICAL-TRIALS; 2ND-LINE TREATMENT; GEFITINIB; THERAPY; CHEMOTHERAPY; EFFICACY; QUALITY; NSCLC;
D O I
10.4103/0019-509X.168957
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: The extent of the benefit of erlotinib in the treatment of advanced nonsmall-cell lung cancer (NSCLC) is still controversial when compared with docetaxel. This meta-analysis was performed to compare the efficacy of erlotinib with docetaxel for different patients with advanced NSCLC. MATERIALS AND METHODS: We searched Cochrane Library, PubMed, CNKI, and identified 23 randomized controlled clinical trials from 2008 to 2015. According to our further full-text screening, 6 clinical trials were included in the final meta-analysis. RESULTS: Six papers were included in this study. The progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and toxicity were included in our outcomes. The pooled hazard ratio (HR) of PFS was 1.57 (95% confidential index [CI] = 1.47-1.69). The pooled HR of OS was 1.66 (95% CI = 1.43-1.92). The pooled risk ratio of ORR was 0.56 (95% CI = 0.35-0.91). The toxicity analysis showed odds ratio = 1.79 (95% CI = 1.20-2.69). CONCLUSIONS: In terms of PFS, OS, and toxicity the effect of erlotinib in the treatment of advanced NSCLC patients is superior to docetaxel.
引用
收藏
页码:E12 / E16
页数:5
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