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Br J Haematol ; 190(3): 437-441, 2020 08.
Article in English | MEDLINE | ID: mdl-32108327

ABSTRACT

Myeloproliferative Neoplasm (MPN), unclassifiable (MPN-U) is a heterogeneous disease with regards to both clinical phenotype and disease course. Patients may initially be asymptomatic or present with leucocytosis or thrombocytosis, anaemia, progressive splenomegaly, constitutional symptom, thromboses or accelerated/blastic phase disease. Treatment strategies are variable and there are no widely accepted consensus management guidelines for MNU-U. Allogeneic Haematopoietic Cell Transplantation (allo-HCT) remains the only curative strategy yet outcomes, to date, are not well defined. We hereby report on the largest retrospective study of patients with MPN-U undergoing allo-HCT, highlighting the potentially curative role and providing clinicians with robust engraftment, GvHD and outcome data to facilitate patient discussion.


Subject(s)
Hematopoietic Stem Cell Transplantation , Myeloproliferative Disorders/therapy , Adult , Aged , Databases, Factual , Female , Follow-Up Studies , Humans , Incidence , Kaplan-Meier Estimate , Male , Middle Aged , Mutation , Myeloproliferative Disorders/genetics , Myeloproliferative Disorders/mortality , Recurrence , Retrospective Studies , Risk , Societies, Scientific , Transplantation Conditioning , Transplantation, Homologous , Treatment Outcome , Young Adult
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