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抗 HER2 靶向治疗转移性 HR 阳性和 HER2 阳性乳腺癌的疗效和安全性:一项贝叶斯网状 Meta 分析。

Efficacy and Safety of Anti-HER2 Targeted Therapy for Metastatic HR-Positive and HER2-Positive Breast Cancer: A Bayesian Network Meta-Analysis.

机构信息

Department of Epidemiology and Health Statistics, School of Public Health, Southeast University, Nanjing 210009, China.

出版信息

Curr Oncol. 2023 Sep 15;30(9):8444-8463. doi: 10.3390/curroncol30090615.

DOI:10.3390/curroncol30090615
PMID:37754530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10528081/
Abstract

Despite the development of HER2-targeted drugs, achieving favorable outcomes for patients with HR+/HER2+MBC remains challenging. This study utilized Bayesian Network Meta-analysis to compare the efficacy and safety of anti-HER2 combination regimens. The primary analysis focused on progression-free survival (PFS), while secondary analyses included objective response rate, overall survival (OS) and the incidence rate of grade 3/4 adverse events (AEs). A comprehensive search across seven databases identified 25 randomized controlled trials for inclusion in this meta-analysis. For patients eligible for endocrinotherapy, our findings revealed that dual-target combined endocrine therapy, such as Her2-mAb+Her2-mAb+Endo (HR = 0.38; 95%CrI: 0.16-0.88) and Her2-mAb+Her2-tki+Endo (HR = 0.45; 95%CrI: 0.23-0.89), significantly improved PFS compared to endocrine therapy alone. According to the surface under the cumulative ranking curves (SUCRAs), Her2-mAb+Her2-mAb+Endo and Her2-mAb+Her2-tki+Endo ranked highest in terms of PFS and OS, respectively. For patients unsuitable for endocrine therapy, anti-HER2 dual-target combined chemotherapy, such as Her2-mAb+Her2-mAb+Chem (HR = 0.76; 95%CrI: 0.6-0.96) and Her2-mAb+Her2-tki+Chem (HR = 0.48; 95%CrI: 0.29-0.81), demonstrated significant improvements in PFS compared to Her2-mAb+Chem. The results were the same when compared with Her2-tki+Chem. According to the SUCRAs, Her2-mAb+Her2-tki+Chem and Her2-mAb+Her2-mAb+Chem ranked highest for PFS and OS, respectively. Subgroup analyses consistently supported these overall findings, indicating that dual-target therapy was the optimal approach irrespective of treatment line.

摘要

尽管已经开发出针对 HER2 的药物,但对于 HR+/HER2+MBC 患者,要获得良好的治疗效果仍然具有挑战性。本研究采用贝叶斯网络荟萃分析比较了抗 HER2 联合方案的疗效和安全性。主要分析侧重于无进展生存期(PFS),次要分析包括客观缓解率、总生存期(OS)和 3/4 级不良事件(AE)的发生率。通过对七个数据库的全面检索,共纳入 25 项随机对照试验进行荟萃分析。对于适合内分泌治疗的患者,我们的研究结果表明,双重靶向联合内分泌治疗,如 Her2-mAb+Her2-mAb+Endo(HR=0.38;95%CI:0.16-0.88)和 Her2-mAb+Her2-tki+Endo(HR=0.45;95%CI:0.23-0.89),与单纯内分泌治疗相比,显著改善了 PFS。根据累积排序曲线下面积(SUCRA),Her2-mAb+Her2-mAb+Endo 和 Her2-mAb+Her2-tki+Endo 在 PFS 和 OS 方面排名最高。对于不适合内分泌治疗的患者,抗 HER2 双重靶向联合化疗,如 Her2-mAb+Her2-mAb+Chem(HR=0.76;95%CI:0.6-0.96)和 Her2-mAb+Her2-tki+Chem(HR=0.48;95%CI:0.29-0.81),与 Her2-mAb+Chem 相比,PFS 显著改善。与 Her2-tki+Chem 相比也是如此。根据 SUCRA,Her2-mAb+Her2-tki+Chem 和 Her2-mAb+Her2-mAb+Chem 在 PFS 和 OS 方面排名最高。亚组分析一致支持这些总体结果,表明无论治疗线如何,双重靶向治疗都是最佳选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/151a/10528081/c03b65ee93bc/curroncol-30-00615-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/151a/10528081/d310c4f8958d/curroncol-30-00615-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/151a/10528081/c03b65ee93bc/curroncol-30-00615-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/151a/10528081/d310c4f8958d/curroncol-30-00615-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/151a/10528081/3fa53153d49c/curroncol-30-00615-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/151a/10528081/6cf4bf9a8d3a/curroncol-30-00615-g003.jpg
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