Abstract

Myeloproliferative neoplasms (MPNs) are characterized by an increased risk of thrombosis and bleeding. Vitamin K antagonists (VKAs) are the historic anticoagulant recommended for use in MPNs. Direct oral anticoagulants (DOACs) are being increasingly used in general and cancer populations. However, DOAC safety and efficacy in MPN patients remains unclear. We characterized real-world practice patterns of DOAC use in MPN patients and evaluated thrombosis and bleeding risk. We conducted a retrospective cohort study of 133 MPN patients prescribed DOACs for venous thromboembolism (VTE), atrial fibrillation, or arterial thromboembolism (ATE). Practice patterns including duration of anticoagulation, dosing, and concomitant use of antiplatelet/cytoreductive agents, were heterogeneous among MPN patients. The 1-year cumulative incidence of thrombosis and bleeding on DOAC was 5.5% (1.5–9.5%) and 12.3% (6.4–18.2%) respectively. In comparison, reported bleeding rates in MPN patients on DOAC and VKAs are 1–3%. On multivariable analysis, prior history of thrombosis, use of dabigatran or edoxaban, and younger age were significantly associated with a higher risk of recurrent thrombosis, while leukocytosis was associated with a higher risk of bleeding on DOAC. The higher-than-expected bleeding rate found in our study indicates the continued need for rigorous evaluation of DOACs in this population.

Highlights

  • Myeloproliferative neoplasms (MPNs) are clonal stem cell disorders and include polycythemia vera (PV), essential thrombocythemia (ET), and myelofibrosis (MF)

  • We evaluated patient characteristics, practice patterns, and thrombosis/bleeding outcomes in a retrospective cohort of 133 MPN patients treated with Direct oral anticoagulants (DOACs)

  • The indications for DOAC use were primarily venous thromboembolism (VTE) followed by atrial fibrillation, with 10% of patients treated for arterial events including stroke

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Summary

Introduction

Myeloproliferative neoplasms (MPNs) are clonal stem cell disorders and include polycythemia vera (PV), essential thrombocythemia (ET), and myelofibrosis (MF). Irrespective of JAK2 V617F driver mutation status, all MPN patients are characterized by dysregulated Janus kinase (JAK)/signal transducer and activator of transcription (STAT) activation, which further contributes to chronic inflammation and cytokine expression [7]. These factors lead to the hypercoagulable state seen in MPN patients, with the highest incidence of thrombotic events seen in PV (5.5% patients per year), followed by ET (1–3% patients per year) and MF (2% patients per year) [8,9,10]. Thrombosis is the leading cause of morbidity and mortality in PV and ET [11]

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