Thrombosis is the most common adverse event in patients with
polycythemia vera (PV) and
essential thrombocythemia (ET). Little is known about the use of nonvitamin K antagonist oral
anticoagulants (NOACs) in patients with myeloproliferative
neoplasms. We sought to evaluate the efficacy and safety of
NOAC in a cohort of patients with PV and ET, who experienced
venous thromboembolism (VTE). We enrolled 48 consecutive patients with PV (70.8%) and ET [median age 67.0 (interquartile range, 58.5-72.0) years], who experienced VTE. Patients received
apixaban (39.6%),
rivaroxaban (33.3%), or
dabigatran (27.1%). During a median follow-up of 30 (interquartile range, 20.5-41.5) months, recurrent thrombotic events and
bleeding were recorded. Four thrombotic events (3.3 per 100 patient-years) were reported. Three
deep vein thrombosis episodes (2.5 per 100 patient-years) were experienced by 2 patients with PV, who received
apixaban (5 mg bid) and
dabigatran (150 mg bid), and 1 patient with ET, who received
dabigatran (150 mg bid). One
ischemic stroke occurred in a patient with PV on
rivaroxaban (20 mg/d). There was 1 major
bleeding (0.8 per 100 patient-years) in a patient with ET on
dabigatran (150 mg bid) and 3 clinically relevant nonmajor
bleeding (2.5 per 100 patient-years): 2 on
rivaroxaban (20 mg/d) and 1 on
apixaban (5 mg bid). We did not observe significant differences related to the type of
NOAC. Three deaths (2.5 per 100 patient-years) unrelated to either VTE or
bleeding were recorded. This study shows that NOACs may be effective and safe as
secondary prevention of VTE in patients with myeloproliferative
neoplasms.