替吉奥与卡培他滨对比治疗进展期胃癌的临床应用Meta分析Meta analysis of S-1 versus Capecitabine for therapy advanced gastric cancer in clinical application
程国良;刘新灵;王维;程刚;
CHENG Guoliang;LIU Xinling;WANG Wei;CHENG Gang;School of Pharmacy,Shenyang Pharmaceutical University;National Chiral Pharmaceutical Engineering Technology Research Center;
摘要(Abstract):
目的通过Meta分析方法探讨替吉奥与卡培他滨对比治疗进展期胃癌的有效性和安全性。方法在Pubmed、Web of science、EBSCO、循证医学图书馆(Cochrane Library)、中国生物医学文献数据库(China Biology Medicine,CBM)、中国期刊全文数据库(China National Knowledge Infrastructure,CNKI)、维普数据库、万方数据库检索国内外研究替吉奥与卡培他滨单药或联合用药对比治疗进展期胃癌的随机对照临床试验,应用Open Meta analyst和Stata 12. 0软件对统计数据进行Meta分析。结果符合纳入和排除标准的文章共27篇,共1 945名患者。Meta分析结果显示,替吉奥组较卡培他滨组的客观缓解率更优(OR=1. 399,95%CI:1. 164-1. 681,P <0. 001),但亚组(替吉奥单药或联合奥沙利铂用药组)之间无统计学差异。两组总生存期和治疗失败时间均无统计学差异;但替吉奥组手足综合征和胃肠道不良反应发生率较低。结论替吉奥相较于卡培他滨在治疗进展期胃癌时的疗效和安全性有优势。
Objective To explore the efficacy and safety of S-1 and Capecitabine of treating advanced gastric cancer in clinical application with Meta analysis. Methods Systematically reviewing the clinical study about S-1 and Capecitabine for the treatment of advanced gastric cancer in the database of PubMed,Web of science,EBSCO,Cochrane Library,CNKI,CBM,VIP and Wanfang. Statistical analysis was completed in Open Meta analysis and Stata 12. 0. Results 1945 patients in 27 studies were included,which satisfied the included and excluded criteria. The results of Meta analysis showed that the response rate of S-1 was better than Capecitabine( OR = 1. 399,95% CI: 1. 164-1. 681,P < 0. 001),but there were statistical difference between subgroup analysis. And the overall survival and time to progression were both similar,but the side effects of HFS and gastrointestinal adverse events in the group of S-1 were less than the group of Capecitabine. Conclusion S-1 can be recommended as the dominant treatment for advanced gastric cancer for more efficacy and less side effects.
关键词(KeyWords):
替吉奥;卡培他滨;胃癌;Meta分析
S-1;Capecitabine;advanced gastric cancer;Meta analysis
基金项目(Foundation):
作者(Authors):
程国良;刘新灵;王维;程刚;
CHENG Guoliang;LIU Xinling;WANG Wei;CHENG Gang;School of Pharmacy,Shenyang Pharmaceutical University;National Chiral Pharmaceutical Engineering Technology Research Center;
DOI: 10.14066/j.cnki.cn21-1349/r.2018.11.011
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- 程国良
- 刘新灵
- 王维
- 程刚
CHENG Guoliang- LIU Xinling
- WANG Wei
- CHENG Gang
- School of Pharmacy
- Shenyang Pharmaceutical University
- National Chiral Pharmaceutical Engineering Technology Research Center
- 程国良
- 刘新灵
- 王维
- 程刚
CHENG Guoliang- LIU Xinling
- WANG Wei
- CHENG Gang
- School of Pharmacy
- Shenyang Pharmaceutical University
- National Chiral Pharmaceutical Engineering Technology Research Center