Effectiveness and safety of Pingxiao capsule as adjuvant therapy in treatment of breast cancer: a systematic review and Meta-analysis.

Yang Yuqing, Chen Yuhuan, L I Chunxiao, Ling Xiao, Wang Panpan, Guo Jing, Zhang Yingying
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Abstract

Objective: To systematically review the effectiveness and safety of Pingxiao capsule adjuvant chemotherapy in the treatment of breast cancer.

Methods: A total of 8 databases including the Cochrane Library, PubMed, EMBASE, Engineering Index, Chinese Biomedical Literature Database, Wanfang database, China National Knowledge Infrastructure Database, and China Science and Technology Journal Database were searched for the Randomized Controlled Trials (RCTs) of Pingxiao capsule combined with chemotherapy in the treatment of breast cancer published before June 2022. Two researchers independently screened the literature, extracted data, and evaluated the risk of bias. R language was used for estimating risks of bias of included studies, data analysis, and plotting.

Results: A total of 15 RCTs involving 1272 patients were included in this study. Meta-analysis results indicated that compared with chemotherapy alone, Pingxiao capsule combined with chemotherapy could significantly improve breast cancer patients' objective response rate of breast cancer patients [rate ratio () = 1.35, 95% confidence interval () (1.12, 1.63), = 0.0017], the disease control rate [=1.16, 95% (1.08, 1.25), < 0.0001], the quality of life [ =1.42, 95% (1.16, 1.74), = 0.007], and the level of the immune cells [CD3+: standardized mean difference () =1.42, 95% (0.76, 2.09), < 0.001; CD4+: =1.18, 95% (0.70, 1.66), < 0.001]. In addition, Pingxiao capsule combined with chemotherapy can also significantly reduce CD8+ level ( < 0.0001) and reduce the symptoms of decreased white blood cell count [ = 0.62, 95% (0.39, 0.85), < 0.0001], and the occurrence of adverse reactions such as gastrointestinal adverse reactions and limb pain ( < 0.05).

Conclusions: Pingxiao capsule can significantly improve the efficacy of chemotherapy, the quality of life and immune function of patients, and reduce the clinical side effects caused by chemotherapy. However, high-quality randomized clinical trials with large samples are required for further verification of these results.

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平消胶囊辅助治疗癌症的有效性和安全性:系统评价和Meta-analysis。
目的:系统评价平消胶囊辅助化疗治疗癌症的有效性和安全性。方法:共8个数据库,包括Cochrane图书馆、PubMed、EMBASE、工程索引、中国生物医学文献数据库、万方数据库、中国国家知识基础设施数据库,检索2022年6月前发表的平消胶囊联合化疗治疗癌症的随机对照试验(RCTs)。两名研究人员对文献进行了独立筛选,提取了数据,并评估了偏倚的风险。R语言用于评估纳入研究、数据分析和绘图的偏倚风险。结果:本研究共纳入15项随机对照试验,涉及1272名患者。Meta-analysis结果表明,与单纯化疗相比,平消胶囊联合化疗可显著提高癌症患者对癌症患者的客观缓解率[比率()=1.35,95%置信区间()(1.12,1.63),=0.0017],疾病控制率[=1.16,95%(1.08,1.25),<0.0001],生活质量[=1.42,95%(1.16,1.74),=0.007]和免疫细胞水平[CD3+:标准化平均差()=1.42,95%CI(0.76,2.09),<0.001;CD4+:=1.18,95%(0.70,1.66),<0.001]。此外,平消胶囊联合化疗还可显著降低CD8+水平(<0.0001),减轻白细胞计数下降的症状[=0.62,95%(0.39,0.85),<0.001],以及胃肠道不良反应和肢体疼痛等不良反应的发生(<0.005),提高患者的生活质量和免疫功能,减少化疗引起的临床副作用。然而,需要用大样本进行高质量的随机临床试验来进一步验证这些结果。
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