| Literature DB >> 32417942 |
Douglas Tremblay1, Myron Schwartz2, Richard Bakst3, Rahul Patel4, Thomas Schiano2, Marina Kremyanskaya1, Ronald Hoffman1, John Mascarenhas5.
Abstract
Myelofibrosis (MF) is a chronic myeloproliferative neoplasm which can lead to massive splenomegaly secondary to extramedullary hematopoiesis. Patients frequently exhibit debilitating symptoms including pain and early satiety, in addition to cellular sequestration causing severe cytopenias. JAK 1/2 inhibitors, such as ruxolitinib and fedratinib, are the mainstay of therapy and produce significant and durable reductions in spleen volume. However, many patients are not eligible for JAK 2 inhibitor therapy or become refractory to treatment over time. Novel therapies are in development that can reduce the degree of splenomegaly for some of these patients. However, splenectomy, splenic irradiation, and partial splenic artery embolization remain valuable therapeutic options in select patients. In this review, we will discuss currently available pharmacologic therapies and describe promising drugs currently in development. We will also delve into the efficacy and safety concerns of splenectomy, splenic irradiation, and partial splenic artery embolization. Finally, we will propose a treatment algorithm to help guide clinicians in the management of symptomatic splenomegaly in patients with MF.Entities:
Keywords: JAK inhibitor; Myelofibrosis; Splenectomy; Splenic artery embolization; Splenic irradiation; Splenomegaly
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Year: 2020 PMID: 32417942 PMCID: PMC7809704 DOI: 10.1007/s00277-020-04069-4
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673