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New England Journal of Medicine· 2013Q1· Clinical trial

Edoxaban versus Warfarin for the Treatment of Symptomatic Venous Thromboembolism

The Hokusai-VTE Investigators

Short summary

Once-daily edoxaban, an oral factor Xa inhibitor, proved non-inferior to warfarin for treating venous thromboembolism and significantly reduced bleeding events.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Edoxaban was non-inferior to warfarin for efficacy in treating venous thromboembolism (3.2% vs. 3.5% recurrence).
  • Edoxaban demonstrated superiority in safety, causing significantly less bleeding (8.5% vs. 10.3%).
  • In patients with pulmonary embolism and right ventricular dysfunction, edoxaban showed a 48% reduction in recurrent VTE compared to warfarin.
  • The study included over 8,000 patients with deep-vein thrombosis or pulmonary embolism.

AI-generated from the title and abstract; the full text is not read.

Abstract

BACKGROUND: Whether the oral factor Xa inhibitor edoxaban can be an alternative to warfarin in patients with venous thromboembolism is unclear. METHODS: In a randomized, double-blind, noninferiority study, we randomly assigned patients with acute venous thromboembolism, who had initially received heparin, to receive edoxaban at a dose of 60 mg once daily, or 30 mg once daily (e.g., in the case of patients with creatinine clearance of 30 to 50 ml per minute or a body weight below 60 kg), or to receive warfarin. Patients received the study drug for 3 to 12 months. The primary efficacy outcome was recurrent symptomatic venous thromboembolism. The principal safety outcome was major or clinically relevant nonmajor bleeding. RESULTS: A total of 4921 patients presented with deep-vein thrombosis, and 3319 with a pulmonary embolism. Among patients receiving warfarin, the time in the therapeutic range was 63.5%. Edoxaban was noninferior to warfarin with respect to the primary efficacy outcome, which occurred in 130 patients in the edoxaban group (3.2%) and 146 patients in the warfarin group (3.5%) (hazard ratio, 0.89; 95% confidence interval [CI], 0.70 to 1.13; P<0.001 for noninferiority). The safety outcome occurred in 349 patients (8.5%) in the edoxaban group and 423 patients (10.3%) in the warfarin group (hazard ratio, 0.81; 95% CI, 0.71 to 0.94; P=0.004 for superiority). The rates of other adverse events were similar in the two groups. A total of 938 patients with pulmonary embolism had right ventricular dysfunction, as assessed by measurement of N-terminal pro-brain natriuretic peptide levels; the rate of recurrent venous thromboembolism in this subgroup was 3.3% in the edoxaban group and 6.2% in the warfarin group (hazard ratio, 0.52; 95% CI, 0.28 to 0.98). CONCLUSIONS: Edoxaban administered once daily after initial treatment with heparin was noninferior to high-quality standard therapy and caused significantly less bleeding in a broad spectrum of patients with venous thromboembolism, including those with severe pulmonary embolism. (Funded by Daiichi-Sankyo; Hokusai-VTE ClinicalTrials.gov number, NCT00986154.).

The authors' abstract, as published at the source. New England Journal of Medicine, 2013 · DOI ↗

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Field: Internal Medicine

Internal MedicineMedicine