Gao Guanghui, Zhou Xinli, Huang Ruofan, Jiang Jingwei, Chu Zhaohui, Zhan Qiong, Liang Xiaohua
Department of Oncology, Huashan Hospital Affiliated to Fudan University, Department of Oncology and Medicine, Shanghai Medical College, Fudan University, Shanghai 200040, China.
Zhongguo Fei Ai Za Zhi. 2009 Jan 20;12(1):38-43. doi: 10.3779/j.issn.1009-3419.2009.01.006.
Platinum plus the third-generation agent doublet chemotherapy is the standard regimens and first line chemotherapy for advanced non-small cell lung cancer (NSCLC). The aim of this study is to determine the benefits and harms of platinum plus gemcitabine or vinorelbine for advanced NSCLC.
The databases PubMed, CENTRAL, EMBASE and Chinese Biomedical Literature database were retrieved by using the key words "non small cell lung cancer" or "Carcinoma, Non Small Cell Lung" so as to search the studies about the randomized controlled clinical trials (RCT) that had compared the gemcitabine plus platinum versus vinorelbine plus platinum for advanced NSCLC. A meta-analysis was conducted.
Nine randomized controlled trials, with total 2 186 patients, were included. The overall response rate and one-year survival rate of the gemcitabine group were not significantly different from that of vinorelbine regimen (RR=0.91, 95%CI: 0.81-1.03, P =0.15; RR=1.06, 95%CI: 0.96-1.18, P =0.27, respectively). The incidence rate of grade 3-4 netropenia, constipation, phlebitis and grade 1-4 neuropathy were higher in vinorelbine group, just like higher incidence rate of grade 3-4 thrombocytopenia in the gemcitabine group.
The curative effects of the gemcitabine or vinorelbine plus platinum regimens are similar. The choice of gemcitabine or vinorelbine depends on the toxicity of the drugs and patients' tolerance.
铂类联合第三代药物的双联化疗是晚期非小细胞肺癌(NSCLC)的标准方案和一线化疗方案。本研究的目的是确定铂类联合吉西他滨或长春瑞滨治疗晚期NSCLC的获益与危害。
通过使用关键词“非小细胞肺癌”或“非小细胞肺癌癌”检索PubMed、CENTRAL、EMBASE和中国生物医学文献数据库,以查找比较吉西他滨联合铂类与长春瑞滨联合铂类治疗晚期NSCLC的随机对照临床试验(RCT)研究。进行荟萃分析。
纳入9项随机对照试验,共2186例患者。吉西他滨组的总缓解率和一年生存率与长春瑞滨方案无显著差异(RR = 0.91,95%CI:0.81 - 1.03,P = 0.15;RR = 1.06,95%CI:0.96 - 1.18,P = 0.27)。长春瑞滨组3 - 4级中性粒细胞减少、便秘、静脉炎和1 - 4级神经病变的发生率较高,而吉西他滨组3 - 4级血小板减少的发生率较高。
吉西他滨或长春瑞滨联合铂类方案的疗效相似。吉西他滨或长春瑞滨的选择取决于药物的毒性和患者的耐受性。