Treatment of Primary Myelofibrosis (PMF)

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The page below is a sample from the LabCE course Myeloproliferative Neoplasms. Access the complete course and earn ASCLS P.A.C.E.-approved continuing education credits by subscribing online.

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Treatment of Primary Myelofibrosis (PMF)

Since the cause of PMF is primarily idiopathic, treatment is targeted toward the symptoms that are being displayed. If a patient is currently asymptomatic, then treatment is reserved until symptoms become evident. Some of these symptomatic treatments include:
  • Blood transfusions for severe anemia
  • Platelet transfusions for thrombocytopenia caused by splenomegaly
  • Immunosuppressant drugs such as hydroxyurea or busulfan to suppress bone marrow's overproduction of cells
The FDA has approved two drugs, ruxolitinib and fedratinib, to treat patients with intermediate or high-risk myelofibrosis. These drugs inhibit the JAK 1 and 2 enzymes.
2. “Primary Myelofibrosis.” NORD (National Organization for Rare Disorders), 24 June 2020, https://rarediseases.org/rare-diseases/primary-myelofibrosis/.