Edoxaban for the Long-Term Therapy of Venous Thromboembolism: Should the Criteria for Dose Reduction be Revised?


Journal

Clinical and translational science
ISSN: 1752-8062
Titre abrégé: Clin Transl Sci
Pays: United States
ID NLM: 101474067

Informations de publication

Date de publication:
01 2021
Historique:
received: 21 02 2020
accepted: 08 08 2020
pubmed: 11 10 2020
medline: 26 10 2021
entrez: 10 10 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33038286
doi: 10.1111/cts.12876
pmc: PMC7877832
doi:

Substances chimiques

Anticoagulants 0
Pyridines 0
Thiazoles 0
edoxaban NDU3J18APO

Banques de données

ClinicalTrials.gov
['NCT02832245']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

335-342

Informations de copyright

© 2020 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of the American Society of Clinical Pharmacology & Therapeutics.

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Auteurs

Giuseppe Camporese (G)

Department of Cardiac, Thoracic, and Vascular Sciences, Unit of Angiology, University Hospital of Padua, Padua, Italy.

Paolo Simioni (P)

Department of Internal Medicine, General Medicine Unit, Thrombotic and Haemorrhagic Disorders Unit, University Hospital of Padua, Padua, Italy.

Pierpaolo Di Micco (P)

Department of Internal Medicine and Emergency Room, Ospedale Buon Consiglio Fatebenefratelli, Naples, Italy.

Carmen Fernández-Capitán (C)

Department of Internal Medicine, Hospital Universitario La Paz, Madrid, Spain.

Agustina Rivas (A)

Department of Pneumonology, Hospital Universitario Araba, Álava, Spain.

Carme Font (C)

Department of Medical Oncology, Hospital Clínic, Barcelona, Spain.

Joan Carles Sahuquillo (JC)

Department of Internal Medicine, Hospital Municipal de Badalona, Barcelona, Spain.

Paula Villares (P)

Department of Internal Medicine, Hospital de Madrid Norte Sanchinarro, Madrid, Spain.

Paolo Prandoni (P)

Department of Cardiovascular Sciences, Vascular Medicine Unit, University of Padua, Padua, Italy.

Manuel Monreal (M)

Department of Internal Medicine, Hospital Germans Trias i Pujol, Universidad Autónoma de Barcelona, Barcelona, Spain.

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