帕妥珠单抗和曲妥珠单抗联合治疗HER-2阳性乳腺癌的临床疗效和安全性荟萃分析

Xiaoyu Zhang, Hui Zhang, Heng Zhang, Yulai Yin, Y. Ren, Xiaoning Kang, Lijun Jin, Jie Bai
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目的:通过荟萃分析,系统评价帕妥珠单抗与曲妥珠单抗联合治疗人表皮生长因子受体2 (HER-2)阳性乳腺癌的临床疗效和安全性。方法:检索PubMed、Embase、Cochrane对照试验中央注册数据库等英文数据库,检索中国国家知识基础设施、万方数据库、中国生物医学文献服务系统等中文数据库,检索比较帕妥珠单抗联合曲妥珠单抗治疗HER-2阳性乳腺癌(实验组)与曲妥珠单抗单独治疗HER-2阳性乳腺癌(对照组)的随机对照试验(RCTs)。文献检索时间为数据库建立至2022年7月。两位审稿人独立筛选文献、提取数据并评估文献质量。meta分析采用Review Manager 5.4软件。结果:meta分析共纳入9项rct,涉及7199例患者。疗效指标结果显示,双靶向治疗HER-2阳性乳腺癌患者的肿瘤进展风险显著低于单抗治疗组[风险比(HR) = 0.68, 95%可信区间(CI) (0.58, 0.79), P0.05],但实验组≥3级腹泻发生率显著高于对照组[相对风险= 2.44,95% CI (1.95, 2.99), P<0.00001]。结论:帕妥珠单抗与曲妥珠单抗联合治疗HER-2阳性乳腺癌患者临床疗效显著,其应用可进一步提高患者的无进展生存期和OS。然而,它也在一定程度上增加了不良反应的风险。因此,在临床实践中,有必要加强对患者相关不良反应的监测和保护。
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Meta-analysis of Clinical Efficacy and Safety of Pertuzumab and Trastuzumab Combined Therapy in HER-2 Positive Breast Cancer
Objective: To systematically evaluate the clinical efficacy and safety of pertuzumab and trastuzumab combined therapy in human epidermal growth factor receptor 2 (HER-2) positive breast cancer through a meta-analysis. Methods: English databases including PubMed, Embase, and the Cochrane Central Register of Controlled Trials, as well as Chinese databases including China National Knowledge Infrastructure, Wanfang Database, and the Chinese Biomedical Literature Service System (Sinomed), were searched for randomized controlled trials (RCTs) comparing pertuzumab and trastuzumab combined therapy (experimental group) with trastuzumab alone (control group) for the treatment of HER-2 positive breast cancer. The literature search time was from the establishment of the database to July 2022. Two reviewers independently screened the literature, extracted data, and assessed the quality of the literature. Meta-analysis was performed using Review Manager 5.4 software. Results: A total of 9 RCTs involving 7199 patients were included in the meta-analysis. The results of the effectiveness indicators showed that the risk of tumor progression in HER-2 positive breast cancer patients receiving dual-targeted therapy was significantly lower than that in patients receiving trastuzumab alone [Hazard ratios (HR) = 0.68, 95% confidence intervals (CI) (0.58, 0.79), P<0.00001]; the overall survival (OS) of HER-2 positive breast cancer patients receiving dual-targeted therapy was significantly longer than that of patients receiving trastuzumab alone [HR=0.73, 95% CI (0.59, 0.88), P<0.0009]. In terms of safety, there was no statistical difference in the incidence of severe adverse events and ≥3 grade neutropenia between the experimental and control groups (P>0.05), but the incidence of ≥3 grade diarrhea in the experimental group was significantly higher than that in the control group [relative risks = 2.44, 95% CI (1.95, 2.99), P<0.00001]. Conclusion: The combined therapy of pertuzumab and trastuzumab has significant clinical efficacy in HER-2 positive breast cancer patients, and its application can further improve patients' progression-free survival and OS. However, it also increases the risk of adverse reactions to a certain extent. Therefore, in clinical practice, it is necessary to strengthen the monitoring and protection of relevant adverse reactions in patients.
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