AI Article Synopsis

  • * The only definitive cure for MF is allogenic stem cell transplantation, but this option is not available to most patients, leaving a significant gap in treatment for MF-related anemia.
  • * Current and potential treatments for anemia in MF include various drugs like luspatercept, momelotinib, and imetelstat, among others, with some strategies exploring combination therapies, particularly with ruxolitinib, to improve outcomes.

Article Abstract

Myelofibrosis (MF) is a clonal hematologic malignancy with progressive bone marrow fibrosis. Clinical manifestations of MF include splenomegaly, constitutional symptoms, and anemia, whose pathogenesis is multifactorial and largely due to ineffective erythropoiesis and is clinically associated with poor quality of life and reduced overall survival. The only curative treatment for MF is allogenic stem cell transplantation; however, few patients are eligible. Disease management strategies for MF-related anemia have limited effectiveness, and Janus kinase (JAK) inhibitors may induce or worsen related anemia. Thus, there is a significant unmet need for the treatment of patients with MF-related anemia. This review summarizes current and emerging treatments for anemia in MF, including luspatercept and KER-050 (transforming growth factor-β ligand traps), momelotinib and pacritinib (JAK inhibitors), pelabresib (a bromodomain extra-terminal domain inhibitor), PRM-151 (an antifibrotic agent), imetelstat (a telomerase inhibitor), and navitoclax (a BCL-2/BCL-xL inhibitor). Therapeutic combinations with ruxolitinib may offer another treatment approach.

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Source
http://dx.doi.org/10.1016/j.critrevonc.2022.103862DOI Listing

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