Thrombocytopenia in patients with myelofibrosis: management options in the era of JAK inhibitor therapy

Myelofibrosis (MF), either appearing de novo (primary MF, PMF) or after a previous diagnosis of essential thrombocythemia or of polycythemia vera, is a progressive disease burdened by symptomatic splenomegaly, debilitating systemic symptoms, ineffective hematopoiesis, and overall reduced survival. P...

Full description

Saved in:
Bibliographic Details
Published inLeukemia & lymphoma Vol. 61; no. 7; pp. 1535 - 1547
Main Authors Benevolo, Giulia, Elli, Elena M., Guglielmelli, Paola, Ricco, Alessandra, Maffioli, Margherita
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 06.06.2020
Subjects
Online AccessGet full text
ISSN1042-8194
1029-2403
1029-2403
DOI10.1080/10428194.2020.1728752

Cover

More Information
Summary:Myelofibrosis (MF), either appearing de novo (primary MF, PMF) or after a previous diagnosis of essential thrombocythemia or of polycythemia vera, is a progressive disease burdened by symptomatic splenomegaly, debilitating systemic symptoms, ineffective hematopoiesis, and overall reduced survival. Patients often present worsening cytopenias, including thrombocytopenia, secondary to progression of the disease as well as to cytoreductive treatment. Patients with MF and thrombocytopenia have few therapeutic options and there is limited information regarding the management of disease in these settings. This article reviews current evidence for the management of patients with MF and thrombocytopenia, in the era of JAK inhibitors.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
ISSN:1042-8194
1029-2403
1029-2403
DOI:10.1080/10428194.2020.1728752