Department of Cardiac, Thoracic, and Vascular Sciences, Unit of Angiology, University Hospital of Padua, Padua, Italy.
Department of Internal Medicine, General Medicine Unit, Thrombotic and Haemorrhagic Disorders Unit, University Hospital of Padua, Padua, Italy.
Clin Transl Sci. 2021 Jan;14(1):335-342. doi: 10.1111/cts.12876. Epub 2020 Oct 10.
Edoxaban is used for venous thromboembolism (VTE) treatment. Real-life data are lacking about its use in long-term therapy. We aimed to assess the efficacy and the safety of edoxaban for long-term VTE treatment in a real-life setting. Patients with VTE included in the Registro Informatizado Enfermedad TromboEmbólica (RIETE) registry, receiving edoxaban 60 or 30 mg daily were prospectively followed up to validate the benefit of using different dosages. The main outcome was the composite of VTE recurrences or major bleeding in patients with or without criteria for dose reduction. Multivariable analysis to identify predictors for the composite outcome was performed. From October 2015 to November 2019, 562 patients received edoxaban for long-term therapy. Most (94%) of the 416 patients not meeting criteria for dose reduction received 60 mg daily, and 92 patients meeting criteria (63%) received 30 mg daily. During treatment, two patients developed recurrent VTE, six had major bleeding and nine died (2 from fatal bleeding). Among patients not meeting criteria for dose reduction, those receiving 30 mg daily had a higher rate of the composite event (hazard ratio (HR) 8.37; 95% confidence interval (CI) 1.12-42.4) and a significant higher mortality rate (HR 31.1; 95% CI 4.63-262) than those receiving 60 mg. Among patients meeting criteria for dose reduction, those receiving 60 mg daily had no events, and a nonsignificantly higher mortality rate (HR 5.04; 95% CI 0.54-133) than those receiving 30 mg daily. In conclusion, edoxaban seems to be effective and safe for long-term VTE treatment in real life. Criteria for dose reduction should be reformulated.
依度沙班用于治疗静脉血栓栓塞症(VTE)。关于其在长期治疗中的应用,实际数据较为缺乏。我们旨在评估依度沙班在真实环境下用于 VTE 长期治疗的疗效和安全性。在注册登记处(RIETE)登记的 VTE 患者,每天接受 60 或 30mg 依度沙班治疗,并前瞻性随访以验证不同剂量的获益。主要结局是无剂量减少标准或有剂量减少标准的患者中 VTE 复发或大出血的复合结局。进行多变量分析以确定复合结局的预测因素。从 2015 年 10 月至 2019 年 11 月,562 例患者接受依度沙班长期治疗。416 例无剂量减少标准的患者中,大多数(94%)接受 60mg 每日治疗,92 例符合标准的患者(63%)接受 30mg 每日治疗。在治疗期间,有 2 例患者出现 VTE 复发,6 例患者出现大出血,9 例患者死亡(2 例死于致命性出血)。在无剂量减少标准的患者中,接受 30mg 每日治疗的患者复合事件发生率更高(风险比(HR)8.37;95%置信区间(CI)1.12-42.4),死亡率显著更高(HR 31.1;95% CI 4.63-262),高于接受 60mg 每日治疗的患者。在有剂量减少标准的患者中,接受 60mg 每日治疗的患者无事件发生,死亡率略高(HR 5.04;95% CI 0.54-133),高于接受 30mg 每日治疗的患者。总之,依度沙班在真实世界中用于 VTE 长期治疗似乎是有效且安全的。应重新制定剂量减少标准。