Biological drivers of clinical phenotype in myelofibrosis Review


Authors: Mascarenhas, J.; Gleitz, H. F. E.; Chifotides, H. T.; Harrison, C. N.; Verstovsek, S.; Vannucchi, A. M.; Rampal, R. K.; Kiladjian, J. J.; Vainchenker, W.; Hoffman, R.; Schneider, R. K.; List, A. F.
Review Title: Biological drivers of clinical phenotype in myelofibrosis
Abstract: Myelofibrosis (MF) is a myeloproliferative disorder that exhibits considerable biological and clinical heterogeneity. At the two ends of the disease spectrum are the myelodepletive or cytopenic phenotype and the myeloproliferative phenotype. The cytopenic phenotype has a high prevalence in primary MF (PMF) and is characterized by low blood counts. The myeloproliferative phenotype is typically associated with secondary MF (SMF), mild anemia, minimal need for transfusion support, and normal to mild thrombocytopenia. Differences in somatic driver mutations and allelic burden, as well as the acquisition of non-driver mutations further influences these phenotypic differences, prognosis, and response to therapies such as JAK2 inhibitors. The outcome of patients with the cytopenic phenotype are comparatively worse and frequently pose a challenge to treat given the inherent exacerbation of cytopenias. Recent data indicate that an innate immune deregulated state that hinges on the myddosome-IRAK-NFκB axis favors the cytopenic myelofibrosis phenotype and offers opportunity for novel treatment approaches. We will review the biological and clinical features of the MF disease spectrum and associated treatment considerations. © 2022, The Author(s).
Keywords: treatment outcome; treatment response; myeloproliferative disorders; myelofibrosis; gene mutation; genetics; myeloproliferative disorder; janus kinase 2; myeloid metaplasia; review; primary myelofibrosis; interferon; phenotype; allele; disease association; anemia; thrombocytopenia; prevalence; immunoglobulin enhancer binding protein; cytokine; biological activity; ligand; blood transfusion; blood cell count; immunity; cytopenia; disease exacerbation; myeloid differentiation factor 88; toll like receptor; rna degradation; humans; prognosis; human; interleukin 1 receptor associated kinase
Journal Title: Leukemia
Volume: 37
Issue: 2
ISSN: 0887-6924
Publisher: Nature Publishing Group  
Date Published: 2023-02-01
Start Page: 255
End Page: 264
Language: English
DOI: 10.1038/s41375-022-01767-y
PUBMED: 36434065
PROVIDER: scopus
PMCID: PMC9898039
DOI/URL:
Notes: Review -- Export Date: 1 March 2023 -- Source: Scopus
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  1. Raajit Kumar Rampal
    342 Rampal
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