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. 2022 Feb 7;6(1):e12657.
doi: 10.1002/rth2.12657. eCollection 2022 Jan.

Thrombosis in myeloproliferative neoplasms during cytoreductive and antithrombotic drug treatment

Affiliations

Thrombosis in myeloproliferative neoplasms during cytoreductive and antithrombotic drug treatment

Tiziano Barbui et al. Res Pract Thromb Haemost. .

Abstract

A state-of-the-art lecture titled "Myeloproliferative Neoplasm-associated Thrombosis" was presented at the ISTH congress in 2021. We summarize here the main points of the lecture with two purposes: to report the incidence rates of major thrombosis in polycythemia vera and essential thrombocythemia and to discuss to what extent cytoreductive therapy and antithrombotic drugs have reduced the incidence of these events. Unfortunately, the incidence rate of thrombosis remains high, ranging between 2 and 5/100 person-years. It is likely that new drugs such as interferon and ruxolitinib can be more efficacious given their cytoreductive and anti-inflammatory activities. Despite prophylaxis with vitamin K antagonists and direct oral anticoagulants after venous thrombosis in either common sites or splanchnic or cerebral sites, the incidence rate is still elevated, as high as 4 to 5/100 person-years. Future studies with new drugs or new strategies should consider thrombosis as the primary endpoint or surrogate biomarkers only if previously validated.

Keywords: antithrombotic drugs; cytoreduction; epidemiology; myeloproliferative neoplasm; thrombosis.

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Figures

FIGURE 1
FIGURE 1
Incidence of thrombosis under hydroxyurea (HU) treatment in polycythemia vera (PV) (A: incidence rate; B: cumulative incidence) and in essential thrombocythemia (ET) (C: cumulative incidence)
FIGURE 2
FIGURE 2
Incidence rate of thrombosis under pegylated interferon‐α (Peg‐INF‐α) treatment in polycythemia vera (PV) and essential thrombocythemia (ET)

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