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复方苦参注射液治疗胃癌:一项系统评价与Meta分析方案

Compound Kushen Injection for gastric cancer: A protocol of systematic review and meta-analysis.

作者信息

Huang Zhihong, Wei Ping

机构信息

Donggang Branch of The First Hospital of Lanzhou University, Lanzhou, China.

出版信息

Medicine (Baltimore). 2019 Nov;98(45):e17927. doi: 10.1097/MD.0000000000017927.

Abstract

BACKGROUND AND AIMS

In recent years, the clinical research about Compound Kushen Injection (CKI) treatment of Gastric cancer (GC) has been increased, but the conclusion is different. The aim of our study is to objective comment the efficacy and adverse effects of CKI treatment of GC.

METHODS

We will retrieve the Randomized controlled trials from the following 6 electronic databases on their inception to April 2019: PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure, Wangfang and Chinese Biomedical Literature Database. Study selection and data collection will be performed independently by 2 reviewers. Cochrane Risk of Bias tool will be used to assess the risk of bias of included studies. The outcomes included overall response rate, complete response rate, 3-year progression-free survival rate, 3-year overall survival rate, and different types of treatment-related adverse events. We calculated the risk ratios as well as their 95% confidence intervals of these outcomes and pooled the results using RevMan 5.2 software and Stata 14.0 software.

RESULTS

The results will be published in a peer-reviewed journal.

CONCLUSION

The results of this review will be widely disseminated through peer-reviewed publications and conference presentations. This evidence may also provide helpful evidence for clinical practice and health policy-makers for the treatment of GC.

PROSPERO REGISTRATION NUMBER

CRD42019133770.

摘要

背景与目的

近年来,关于复方苦参注射液(CKI)治疗胃癌(GC)的临床研究有所增加,但结论不一。本研究的目的是客观评价CKI治疗GC的疗效和不良反应。

方法

我们将检索以下6个电子数据库从建库至2019年4月的随机对照试验:PubMed、Embase、Cochrane图书馆、中国知网、万方和中国生物医学文献数据库。由2名研究者独立进行研究筛选和数据收集。采用Cochrane偏倚风险工具评估纳入研究的偏倚风险。结局指标包括总缓解率、完全缓解率、3年无进展生存率、3年总生存率以及不同类型的治疗相关不良事件。我们计算这些结局指标的风险比及其95%置信区间,并使用RevMan 5.2软件和Stata 14.0软件汇总结果。

结果

结果将发表在同行评审期刊上。

结论

本综述的结果将通过同行评审出版物和会议报告广泛传播。该证据也可能为GC治疗的临床实践和卫生政策制定者提供有用的证据。

PROSPERO注册号:CRD42019133770。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ec/6855605/604c4b333bca/medi-98-e17927-g002.jpg

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