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Comparative efficacy of everolimus plus exemestane versus fulvestrant for hormone-receptor-positive advanced breast cancer following progression/ recurrence after endocrine therapy: A network meta-analysis

机译:依维莫司加依西美坦与氟维司群对内分泌治疗后进展/复发后激素受体阳性晚期乳腺癌的比较疗效:网络荟萃分析

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Postmenopausal women with advanced breast cancer recurring/progressing on or after initial (adjuvant or first-line) endocrine therapy may be treated multiple times with one of several endocrine or combinatorial targeted treatment options before initiating chemotherapy. In the absence of direct head-to-head comparisons of these treatment options, an indirect comparison can inform treatment choice. This network meta-analysis compared the efficacy of everolimus plus exemestane with that of fulvestrant 250 and 500 mg in the advanced breast cancer setting following adjuvant or first-line endocrine therapy. The reported hazard ratios (HRs) for progression-free survival (PFS) or time to progression from six studies that formed a network to compare everolimus plus exemestane (BOLERO-2 trial) with fulvestrant were analyzed by means of a Bayesian network meta-analysis. In the primary comparison (PFS analysis based on the local review of disease progression from BOLERO-2 with the data from the other studies), everolimus plus exemestane appeared to be more efficacious than both fulvestrant 250 mg (HR = 0.47; 95 % credible interval [CrI] 0.38-0.58) and 500 mg (HR = 0.59; 95 % CrI 0.45-0.77). Similar results were obtained in an alternate comparison based on central review of disease progression from BOLERO-2 with the data from the other studies (HR = 0.40; 95 % CrI 0.31-0.51 and HR = 0.50; 95 % CrI 0.37-0.67, respectively), and in a subgroup analysis of patients who had received prior aromatase inhibitor therapy (HR = 0.47; 95 % CrI 0.38-0.58 and HR = 0.55; 95 % CrI 0.40-0.76, respectively). These results suggest that everolimus plus exemestane may be more efficacious than fulvestrant in patients with advanced breast cancer who progress on or after adjuvant or first-line therapy with a nonsteroidal aromatase inhibitor.
机译:初次(辅助或一线)内分泌治疗后或之后复发/进展的晚期乳腺癌的绝经后妇女可以在开始化疗之前用几种内分泌或组合靶向治疗方案中的一种进行多次治疗。在没有直接比较这些治疗方案的情况下,间接比较可以告知治疗选择。该网络荟萃分析比较了依维莫司加依西美坦与氟维司群250和500 mg在晚期乳腺癌患者中在辅助或一线内分泌治疗后的疗效。通过贝叶斯网络荟萃分析分析了六项研究的报告的无进展生存期(PFS)或进展时间的危险比(HRs),该研究形成了将依维莫司加依西美坦与氟维司群进行比较的网络(BOLERO-2试验) 。在主要比较中(PFS分析基于对BOLERO-2疾病进展的局部评估以及其他研究的数据),依维莫司加依西美坦似乎比两种氟维司群250 mg更有效(HR = 0.47; 95%可信区间[CrI] 0.38-0.58)和500 mg(HR = 0.59; 95%CrI 0.45-0.77)。在对来自BOLERO-2疾病进展的集中评估以及其他研究的数据的替代比较中获得了相似的结果(HR = 0.40; 95%CrI 0.31-0.51和HR = 0.50; 95%CrI 0.37-0.67 ),并在接受亚芳香酶抑制剂治疗的患者中进行亚组分析(分别为HR = 0.47; 95%CrI 0.38-0.58和HR = 0.55; 95%CrI 0.40-0.76)。这些结果表明,依维莫司加依西美坦比氟维司群比在非甾体芳香酶抑制剂辅助治疗或一线治疗后进展的晚期乳腺癌患者中更有效。

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