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Polycythemia vera and essential thrombocythemia: a nationwide population-based study on treatment patterns, vascular complications and survival
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine.ORCID iD: 0000-0002-9984-3520
Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
Division of Hematology, Department of Medicine, NU Hospital Group, Uddevalla, Sweden.
Umeå University, Faculty of Medicine, Department of Epidemiology and Global Health.ORCID iD: 0000-0001-6206-3099
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2026 (English)In: European Journal of Haematology, ISSN 0902-4441, E-ISSN 1600-0609Article in journal (Refereed) Epub ahead of print
Abstract [en]

Background: Polycythemia vera (PV) and essential thrombocythemia (ET) are associated with a well-recognized increased risk of thrombotic events, bleeding, and all-cause mortality, but the frequency of these outcomes during treatment has rarely been assessed in large cohorts.

Methods: In this nationwide, population-based study, we analyzed 2604 PV and 3141 ET patients using multiple Swedish health care registers, covering 43 612 patient-years. Rates of arterial and venous events, major bleeding, and all-cause mortality (ACM) were evaluated across therapies.

Results: Unexpectedly, 42.3% of low-risk PV patients and 29.7% of very low/low-risk ET patients received hydroxyurea (HU) during follow-up. High-risk PV patients treated with interferon (IFN) exhibited the lowest arterial event rate (2.21 per 100 patient-years). In high-risk ET, patients with IFN therapy experienced the lowest arterial and venous event rates (1.55 and 0.44 per 100 patient-years). Advanced age and leukocytosis at diagnosis independently predicted thrombosis, bleeding, and ACM in both PV and ET. Multivariable analysis showed that HU and IFN were associated with reduced ACM risk; HU also conferred protection against thromboembolism and major bleeding.

Conclusion: This study highlights risk factors associated with complications during treatment in a real-world context and reinforces the role of HU and IFN as first-line therapies in PV and ET.

Place, publisher, year, edition, pages
John Wiley & Sons, 2026.
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Hematology
Identifiers
URN: urn:nbn:se:umu:diva-248998DOI: 10.1111/ejh.70113ISI: 001660804400001PubMedID: 41531010Scopus ID: 2-s2.0-105027651986OAI: oai:DiVA.org:umu-248998DiVA, id: diva2:2034853
Funder
Norrbotten County CouncilVisare NorrThe Swedish Stroke AssociationBlodcancerförbundetSwedish Association of Persons with Neurological DisabilitiesAvailable from: 2026-02-03 Created: 2026-02-03 Last updated: 2026-02-03

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Enblom, AnneliHolmberg, HenrikLiljeholm, MariaSjälander, Anders

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