Suppr超能文献

CDK4/6 和 PI3K/AKT/mTOR 抑制剂作为激素受体阳性、HER-2 阴性转移性乳腺癌绝经后患者二线治疗的疗效和安全性:一项网络荟萃分析。

Efficacy and safety of CDK4/6 and PI3K/AKT/mTOR inhibitors as second-line treatment in postmenopausal patients with hormone receptor-positive, HER-2-negative metastatic breast cancer: a network meta-analysis.

机构信息

Department of Obstetrics and Gynecology, Ditmanson Medical Foundation Chiayi Christian Hospital, Chiayi, Taiwan.

Department of Radiation Oncology, An Nan Hospital, China Medical University, Tainan, Taiwan.

出版信息

Expert Opin Drug Saf. 2021 Aug;20(8):949-957. doi: 10.1080/14740338.2021.1931116. Epub 2021 Aug 11.

Abstract

BACKGROUND

We compared the efficacy and safety of combinations of cyclin-dependent kinase 4/6 (CDK4/6) inhibitors and PI3K/AKT/mTOR inhibitors as second-line treatment in postmenopausal women with HR, HER2 metastatic breast cancer.

METHODS

We searched the Medline, Embase, and Cochrane Library electronic databases for phase II/III randomized trials evaluating CDK4/6 and PI3K/AKT/mTOR inhibitors plus fulvestrant. We compared the results with a network meta-analysis. Study quality was assessed following the GRADE approach. Outcomes of interest were progression-free survival, overall response rate, overall survival and G3-4 adverse drug events (ADEs).

RESULTS

Eight RCTs were identified in the network meta-analysis. PFS was significantly improved by treatment with abemaciclib plus fulvestrant and ribociclib plus fulvestrant compared to pictilisib plus fulvestrant. The ORR following treatment with abemaciclib plus fulvestrant, ribociclib plus fulvestrant, palbociclib plus fulvestrant, buparlisib plus fulvestrant, and alpelisib plus fulvestrant significantly differed from that observed following treatment with placebo plus fulvestrant. In terms of OS, compared with placebo plus fulvestrant, abemaciclib plus fulvestrant, ribociclib plus fulvestrant, and buparlisib plus fulvestrant had a significant difference. The risks of ADEs were similar among three CDK4/6 inhibitors.

CONCLUSION

As second-line treatment, three CDK4/6 inhibitors showed superior clinical efficacy compared to other PI3K/AKT/mTOR inhibitors with comparable safety profiles.

摘要

背景

我们比较了 CDK4/6(细胞周期蛋白依赖性激酶 4/6)抑制剂和 PI3K/AKT/mTOR 抑制剂联合作为 HR、HER2 转移性乳腺癌绝经后妇女二线治疗的疗效和安全性。

方法

我们检索了 Medline、Embase 和 Cochrane 图书馆电子数据库中的 II/III 期随机临床试验,评估了 CDK4/6 和 PI3K/AKT/mTOR 抑制剂联合氟维司群的疗效。我们将结果与网络荟萃分析进行了比较。采用 GRADE 方法评估研究质量。主要观察终点为无进展生存期、总缓解率、总生存期和 G3-4 级不良药物事件(AE)。

结果

网络荟萃分析共纳入 8 项 RCT。与 pictilisib 联合氟维司群相比,abemaciclib 联合氟维司群和 ribociclib 联合氟维司群显著改善了 PFS。abemaciclib 联合氟维司群、ribociclib 联合氟维司群、palbociclib 联合氟维司群、buparlisib 联合氟维司群和 alpelisib 联合氟维司群治疗的 ORR 显著高于安慰剂联合氟维司群。在 OS 方面,与安慰剂联合氟维司群相比,abemaciclib 联合氟维司群、ribociclib 联合氟维司群和 buparlisib 联合氟维司群有显著差异。三种 CDK4/6 抑制剂的 AE 风险相似。

结论

作为二线治疗,三种 CDK4/6 抑制剂与其他 PI3K/AKT/mTOR 抑制剂相比具有更好的临床疗效,且安全性相当。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验