Abemaciclib increases the risk of venous thromboembolism in breast cancer: Integrate meta-analysis, pharmacovigilance database analysis, and in vitro validation

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL
Manqi Hua , Fei Xiong , Shan Chong , Zhuo Zhang , Qianxin Liu , Jingyi Hou , Zhiqi Zhang , Zhichun Gu , Xiangli Cui , Yimin Cui , Ling Xu , Qian Xiang
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引用次数: 0

Abstract

Background

Recently, cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) have emerged as a novel treatment strategy for breast cancer. However, increasing reports of CDK4/6i-associated venous thromboembolism (VTE) have garnered attention. This study assessed CDK4/6i-associated VTE in breast cancer, and examined the effect of CDK4/6i on platelet/coagulation function for the first time in vitro.

Methods

PubMed and Embase databases were searched for studies published from the establishment of the database to December 31, 2022 for randomized controlled trials (RCTs) and real-world studies of CDK4/6i in patients with breast cancer, and the data obtained from the included studies were used for meta-analysis. A disproportionality analysis by extracting adverse drug reaction signals of CDK4/6i-associated VTE from the FDA Adverse Event Reporting System (FAERS) database was also conducted. Additionally, the in vitro effect of CDK4/6i on platelet function was assessed based on platelet aggregation tests and flow cytometry, and coagulation function was assessed based on the blood clotting function test.

Findings

A total of 16,903 patients in 13 RCTs and 6,490 patients in 9 real-world studies were included in the meta-analysis. In RCTs, VTE occurred in 193 (2.1 %) and 55 (0.7 %) patients in the CDK4/6i and control groups, respectively. In real-world studies, the aggregate incidence rate of VTE was 4.2 % (95 % CI: 2.1, 6.3). The meta-analysis of RCTs revealed that abemaciclib (Odds ratio [OR]: 4.40 [95 % CI: 2.74,7.05], p < 0.001) and palbociclib (OR: 2.35 [95 % CI: 1.34, 4.12], p < 0.01) significantly increased the risk of VTE in patients with breast cancer compared to placebo. FAERS database analysis revealed that abemaciclib (reporting odds ratio [ROR]: 1.63 [95 % CI: 1.36, 1.97]; IC025: 0.67) and ribociclib (ROR: 1.17 [95 % CI: 1.0, 1.39]; IC025: 0.18) demonstrated a significantly increased signal of VTE. Similarly, findings from in vitro experiments demonstrated that abemaciclib enhanced agonist-induced platelet activation, especially when collagen was used as the inducer, and this effect became more prominent with increasing its concentration.

Interpretation

Use of abemaciclib may increase the risk of VTE in patients with breast cancer, which may be partially attributed to the effect of abemaciclib on platelet function. Close monitoring of VTE occurrence is highly recommended while using abemaciclib, especially in patients at a high risk of VTE.

Abemaciclib 会增加乳腺癌患者的静脉血栓栓塞风险:整合荟萃分析、药物警戒数据库分析和体外验证
背景最近,细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6i)已成为乳腺癌的一种新型治疗策略。然而,越来越多关于CDK4/6i相关静脉血栓栓塞症(VTE)的报道引起了人们的关注。本研究评估了CDK4/6i相关的乳腺癌VTE,并首次在体外检测了CDK4/6i对血小板/凝血功能的影响。方法在PubMed和Embase数据库中检索了自数据库建立至2022年12月31日期间发表的关于CDK4/6i治疗乳腺癌患者的随机对照试验(RCT)和真实世界研究,并对纳入的研究数据进行了荟萃分析。通过从美国食品药品管理局不良事件报告系统(FAERS)数据库中提取与CDK4/6i相关的VTE的药物不良反应信号,还进行了比例失调分析。此外,还根据血小板聚集试验和流式细胞术评估了 CDK4/6i 对血小板功能的体外影响,并根据凝血功能试验评估了凝血功能。在 RCT 研究中,CDK4/6i 组和对照组分别有 193 例(2.1%)和 55 例(0.7%)患者发生 VTE。在真实世界研究中,VTE的总发生率为4.2%(95% CI:2.1, 6.3)。RCT荟萃分析显示,与安慰剂相比,abemaciclib(Odds ratio [OR]:4.40 [95 % CI:2.74,7.05],p < 0.001)和palbociclib(OR:2.35 [95 % CI:1.34,4.12],p < 0.01)显著增加了乳腺癌患者发生VTE的风险。FAERS数据库分析显示,abemaciclib(报告几率比[ROR]:1.63 [95 % CI:1.36, 1.97];IC025:0.67)和ribociclib(ROR:1.17 [95 % CI:1.0, 1.39];IC025:0.18)显示VTE信号显著增加。同样,体外实验结果表明,阿贝昔单抗增强了激动剂诱导的血小板活化,尤其是当使用胶原蛋白作为诱导剂时,这种效应随着浓度的增加而变得更加突出。强烈建议在使用阿柏西尼期间密切监测VTE的发生,尤其是VTE高风险患者。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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