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新型 Xa 因子抑制剂依度沙班与华法林治疗心房颤动患者的比较评估:心房颤动-溶栓治疗心肌梗死 48 次新一代 Xa 因子有效抗凝试验(ENGAGE AF-TIMI 48)的设计和原理。

Evaluation of the novel factor Xa inhibitor edoxaban compared with warfarin in patients with atrial fibrillation: design and rationale for the Effective aNticoaGulation with factor xA next GEneration in Atrial Fibrillation-Thrombolysis In Myocardial Infarction study 48 (ENGAGE AF-TIMI 48).

机构信息

TIMI Study Group, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Am Heart J. 2010 Oct;160(4):635-41. doi: 10.1016/j.ahj.2010.06.042.

Abstract

BACKGROUND

Vitamin K antagonists have been the standard oral antithrombotic used for more than a half century for prevention and treatment of thromboembolism. Their limitations include multiple food and drug interactions and need for frequent monitoring and dose adjustments. Edoxaban is a selective and direct factor Xa inhibitor that may provide effective, safe, and more convenient anticoagulation.

STUDY DESIGN

ENGAGE AF-TIMI 48 is a phase 3, randomized, double-blind, double-dummy, multinational, noninferiority design megatrial comparing 2 exposure strategies of edoxaban to warfarin. Approximately 20,500 subjects will be randomized to edoxaban high exposure (60 mg daily, adjusted for drug clearance), edoxaban low exposure (30 mg daily, adjusted for drug clearance), or warfarin titrated to an international normalized ratio of 2.0 to 3.0. The edoxaban strategies provide for dynamic dose reductions in subjects with anticipated increased drug exposure. Blinded treatment is maintained through the use of sham international normalized ratios in patients receiving edoxaban. Eligibility criteria include electrical documentation of atrial fibrillation ≤12 months and a CHADS(2) score ≥2. Randomization is stratified by CHADS(2) score and anticipated drug exposure. The primary objective is to determine whether edoxaban is noninferior to warfarin for the prevention of stroke and systemic embolism. The primary safety end point is modified International Society on Thrombosis and Haemostasis major bleeding. Recruitment began in November 2008. The expected median follow-up is 24 months.

CONCLUSIONS

ENGAGE AF-TIMI 48 is a phase 3 comparison of the novel oral factor Xa inhibitor edoxaban to warfarin for the prevention of thromboembolism in patients with atrial fibrillation.

摘要

背景

维生素 K 拮抗剂作为标准的口服抗血栓药物,已经在预防和治疗血栓栓塞方面使用了半个多世纪。其局限性包括多种食物和药物相互作用,需要频繁监测和剂量调整。依度沙班是一种选择性和直接的 Xa 因子抑制剂,可能提供有效的、安全的、更方便的抗凝治疗。

研究设计

ENGAGE AF-TIMI 48 是一项 3 期、随机、双盲、双模拟、多国、非劣效性设计的大型临床试验,比较了依度沙班与华法林的 2 种暴露策略。大约 20500 名受试者将被随机分配到依度沙班高暴露组(每日 60mg,根据药物清除率调整剂量)、依度沙班低暴露组(每日 30mg,根据药物清除率调整剂量)或华法林组(调整至国际标准化比值为 2.0 至 3.0)。依度沙班的策略为预计药物暴露增加的受试者提供动态剂量减少。接受依度沙班治疗的患者通过使用模拟国际标准化比值保持盲法治疗。入选标准包括 12 个月内心房颤动的电记录和 CHADS(2)评分≥2 分。随机分组根据 CHADS(2)评分和预计药物暴露分层。主要目的是确定依度沙班是否不劣于华法林预防卒中和全身性栓塞。主要安全性终点为改良国际血栓与止血学会大出血。招募于 2008 年 11 月开始。预计中位随访时间为 24 个月。

结论

ENGAGE AF-TIMI 48 是一项 3 期临床试验,比较了新型口服 Xa 因子抑制剂依度沙班与华法林预防心房颤动患者血栓栓塞。

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