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Claire N. Harrison

Researcher at Guy's and St Thomas' NHS Foundation Trust

Publications -  511
Citations -  24605

Claire N. Harrison is an academic researcher from Guy's and St Thomas' NHS Foundation Trust. The author has contributed to research in topics: Ruxolitinib & Myelofibrosis. The author has an hindex of 66, co-authored 424 publications receiving 19843 citations. Previous affiliations of Claire N. Harrison include St Thomas' Hospital & National Health Service.

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Safety and efficacy of fedratinib, a selective oral inhibitor of Janus kinase‐2 (JAK2), in patients with myelofibrosis and low pretreatment platelet counts

TL;DR: Evaluated data indicate that fedratinib 400 mg/day is safe and effective in patients with myelofibrosis and low pretreatment platelet counts, and no initial fedrat inib dose adjustment is required for these patients.
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The Medical Research Council PT1 Trial in Essential Thrombocythemia.

TL;DR: The MRC PT1 trial demonstrates that, compared to Hu+asp, Ag+asp is associated with an excess rate of arterial thrombosis, major hemorrhage and myelofibrotic transformation but decreased venous thromBosis, and suggest that Hu should remain first-line therapy in patients with ET at high risk for vascular events.
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Aspirin in low-risk essential thrombocythemia, not so simple after all?

TL;DR: It is concluded that antiplatelet therapy reduces the incidence of enous thrombosis in JAK2-positive patients and the rate of arterial hrombotic events in patients with associated cardiovascular risk factors; n the remaining low-risk patients observation may be an adequate ption.
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Pacritinib Is a Potent ACVR1 Inhibitor with Significant Anemia Benefit in Patients with Myelofibrosis

TL;DR: Pacritinib is a potent ACVR1 inhibitor with a clinically important impact on transfusion independence in patients with myelofibrosis (MF) as discussed by the authors , which has been postulated that inhibition of activin A receptor, type I (ACVR1), which mediates hepcidin production, is able to overcome the JAK2 inhibitor class effect on anemia.