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.
Expert Opin Drug Saf. 2021 Aug;20(8):949-957. doi: 10.1080/14740338.2021.1931116. Epub 2021 Aug 11.
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.
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).
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.
As second-line treatment, three CDK4/6 inhibitors showed superior clinical efficacy compared to other PI3K/AKT/mTOR inhibitors with comparable safety profiles.
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。
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)。
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。
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。