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A retrospective real-world study of the current treatment pathways for myelofibrosis in the United Kingdom: the REALISM UK study

Last Updated: Wednesday, June 1, 2022

Using medical record data from 200 patients with myelofibrosis in the United Kingdom, researchers determined that, at diagnosis, symptoms and prognostic scores were poorly documented and patient-reported outcome measures were not frequently used. For the majority of patients (53.5%), watch and wait was the first management strategy used, with hydroxycarbamide and ruxolitinib being the most commonly used active treatments. Further, only 5% of patients proceeded to allogeneic transplant.

Therapeutic Advances in Hematology
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British Journal of Haematology

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Significant association of cutaneous adverse events with hydroxyurea: results from a prospective non-interventional study in BCR-ABL1-negative myeloproliferative neoplasms (MPN) - on behalf of the German Study Group-MPN

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Patient outcomes in myeloproliferative neoplasm-related thrombosis: Insights from the National Inpatient Sample

British Journal of Haemtology

Real‐world non‐interventional long‐term post‐authorisation safety study of ruxolitinib in myelofibrosis

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Depressive symptoms and myeloproliferative neoplasms: Understanding the confounding factor in a complex condition

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Developing strategies to reduce the duration of therapy for patients with myeloproliferative neoplasms

European Society for Medical Oncology (ESMO) Congress 2021 Abstract

Final results of a phase II study of tipifarnib in chronic myelomonocytic leukemia (CMML) and other myelodysplastic/myeloproliferative neoplasms (MDS/MPN)

European Society for Medical Oncology (ESMO) Congress 2021 Abstract

Treatment outcomes and antibody immunity to SARS-CoV-2 in patients with hematological malignancies

Annals of Hematology

Evaluation of the need for cytoreduction and its potential carcinogenicity in children and young adults with myeloproliferative neoplasms

Clinical Lymphoma Myeloma and Leukemia

Mortality and causes of death of patients with polycythemia vera: analysis of the REVEAL prospective, observational study

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