Xue Zhengbiao, Liao Song, Fan Haiye, Shen Yu, Nie Zhi
Department of Critical Care Medicine, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Intensive Care Medicine Department, Dayu County People's Hospital, Ganzhou, Jiangxi, China.
Clin Appl Thromb Hemost. 2025 Jan-Dec;31:10760296251335967. doi: 10.1177/10760296251335967. Epub 2025 Apr 15.
BackgroundAtrial fibrillation (AF) is a leading cause of stroke, necessitating effective anticoagulation. While direct oral anticoagulants (DOACs) have improved stroke prevention, bleeding risks remain a concern. Factor XI/XIa inhibitors, targeting the intrinsic coagulation pathway, offer potential for reduced bleeding, although questions remain regarding their efficacy. This systematic review evaluates the efficacy and safety of Factor XI/XIa inhibitors compared to DOACs in AF patients.MethodsWe conducted a systematic review of randomized controlled trials (RCTs) comparing Factor XI/XIa inhibitors with DOACs in AF patients, identified through PubMed and Embase up to January 2025. Data were synthesized narratively due to heterogeneity in study designs and outcomes.ResultsThree RCTs (AZALEA-TIMI 71, OCEANIC-AF, PACIFIC-AF) involving 16 852 patients were included. Factor XI/XIa inhibitors (abelacimab and asundexian) demonstrated significant reductions in bleeding compared to DOACs. In AZALEA-TIMI 71, abelacimab reduced major or clinically relevant non-major bleeding by 62%-69% versus rivaroxaban. In PACIFIC-AF, asundexian reduced bleeding by 50%-84% compared to apixaban. However, OCEANIC-AF showed asundexian was inferior in stroke prevention, with a 3.8-fold higher risk of stroke or systemic embolism compared to apixaban, leading to early trial termination. Abelacimab showed a trend toward higher ischemic stroke rates abelacimab (150 mg: 1.21 vs 0.59 events/100 person-years; and 90 mg: 1.24 vs 0.59 events/100 person-years), though not statistically significant.ConclusionFactor XI/XIa inhibitors significantly reduce bleeding risk in AF patients compared to DOACs, but their thrombotic efficacy remains uncertain. While promising, further research is needed to optimize their use.
背景
心房颤动(AF)是中风的主要原因,因此需要有效的抗凝治疗。虽然直接口服抗凝剂(DOACs)改善了中风预防,但出血风险仍然令人担忧。靶向内源性凝血途径的因子XI/XIa抑制剂有可能减少出血,尽管其疗效仍存在疑问。本系统评价评估了在房颤患者中,与DOACs相比,因子XI/XIa抑制剂的疗效和安全性。
方法
我们对截至2025年1月通过PubMed和Embase检索到的比较因子XI/XIa抑制剂与DOACs在房颤患者中的随机对照试验(RCTs)进行了系统评价。由于研究设计和结果的异质性,数据采用叙述性综合分析。
结果
纳入了三项RCTs(AZALEA-TIMI 71、OCEANIC-AF、PACIFIC-AF),共16852例患者。与DOACs相比,因子XI/XIa抑制剂(阿贝西单抗和阿孙德西安)显示出血显著减少。在AZALEA-TIMI 71中,与利伐沙班相比,阿贝西单抗使主要或临床相关非主要出血减少了62%-69%。在PACIFIC-AF中,与阿哌沙班相比,阿孙德西安使出血减少了50%-84%。然而,OCEANIC-AF显示阿孙德西安在预防中风方面较差,与阿哌沙班相比,中风或全身性栓塞风险高3.8倍,导致试验提前终止。阿贝西单抗显示缺血性中风发生率有升高趋势(150mg:1.21比0.59事件/100人年;90mg:1.24比0.59事件/100人年),但无统计学意义。
结论
与DOACs相比,因子XI/XIa抑制剂显著降低房颤患者的出血风险,但其血栓形成疗效仍不确定。虽然前景广阔,但仍需进一步研究以优化其使用。