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Shenqi Fuzheng Injection in the Treatment of Breast Cancer: A Meta-analysis of Randomized Controlled Trials

机译:参芪扶正注射液治疗乳腺癌的Meta分析

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摘要

>Objective: This meta-analysis synthesized the available evidence on the effectiveness and safety of Shenqi Fuzheng injection (SQFZI) combined with chemotherapy for breast cancer. >Method: A comprehensive systematic literature search was conducted to identify the randomized controlled trials (RCTs) on breast cancer treated by SQFZI in several electronic database up to October 29, 2017. The included RCTs were assessed using the Cochrane Collaboration tool; data were extracted and analyzed via RevMan 5.3 and Stata 13.0 software. >Results: A total of 31 eligible RCTs comprising 2543 participants were selected in this present meta-analysis. The results demonstrated that compared with receiving conventional chemotherapy alone, SQFZI treatment combined with chemotherapy was more efficient in improving clinical total effective rate (relative risk [RR] = 1.31, 95% CI 1.19-1.44, P < .00001) and performance status (RR = 2.23, 95% CI 1.88-2.65, P < .00001). Additionally, SQFZI combined with chemotherapy was capable of enhancing immune function and alleviating adverse drug reactions for patients with breast cancer. >Conclusions: The current evidence suggested that using SQFZI as an adjunct treatment to chemotherapy may be preferable for patients with breast cancer compared to chemotherapy alone. Because of the limitations of the quantities and qualities of included RCTs, more well-designed RCTs are needed to further support our conclusion.
机译:>目的:这项荟萃分析综合了参芪扶正注射液(SQFZI)联合化学疗法治疗乳腺癌的有效性和安全性的现有证据。 >方法:进行了全面的系统文献检索,以鉴定截至2017年10月29日在多个电子数据库中使用SQFZI治疗的乳腺癌的随机对照试验(RCT)。使用Cochrane对纳入的RCT进行了评估协作工具;通过RevMan 5.3和Stata 13.0软件提取和分析数据。 >结果:在本荟萃分析中,总共选择了31个合格的RCT,包括2543名参与者。结果表明,与单独接受常规化疗相比,SQFZI治疗联合化疗在改善临床总有效率(相对风险[RR] = 1.31,95%CI 1.19-1.44,P <.00001)方面更有效( RR = 2.23,95%CI 1.88-2.65,P <.00001)。此外,SQFZI联合化学疗法能够增强乳腺癌患者的免疫功能并减轻药物不良反应。 >结论:目前的证据表明,与单纯化疗相比,SQFZI作为乳腺癌的辅助治疗可能更适合乳腺癌患者。由于所包括的随机对照试验的数量和质量的局限性,需要更精心设计的随机对照试验来进一步支持我们的结论。

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