Polycythemia vera: Current pharmacotherapy and future directions

Benjamin Hensley, Holly Geyer, Ruben Mesa

Research output: Contribution to journalReview article

13 Scopus citations

Abstract

Introduction: In the past, management of polycythemia vera (PV) was built upon a cornerstone of control over erythrocytosis, through therapeutic phlebotomy, as well as the use of low-dose aspirin. Historically, selected patients were managed with additional cytoreductive therapies to decrease the risk of vascular events, with the recognition that these therapies likely did not impede progression. Areas covered: Recent clinical trials have demonstrated, in a randomized fashion, that optimal control of the hematocrit to target levels < 45% are important for decreasing the risk of vascular events. We are identifying that our historical set of cytoreductive agents, such as hydroxyurea, may be replaced in the future. The first candidate is pegylated interferon alpha-2a, which is demonstrating the ability to control vascular events and control extended hematopoiesis, while potentially having impact on fibrotic progression and Janus kinase 2 (JAK2) V1617F mutant allele burden. Ruxolitinib, as well as other JAK2 inhibitors in development, are demonstrating that this class of agents is making a very meaningful impact on the risk of vascular events in PV, controlling expanded hematopoiesis, as well as helping with symptomatic burden. Expert opinion: Future goals include attaining a better understanding of the specific roles of JAK inhibitor therapy and whether their use in combination with standard therapies offers greater efficacy than single agents alone.

Original languageEnglish (US)
Pages (from-to)609-617
Number of pages9
JournalExpert Opinion on Pharmacotherapy
Volume14
Issue number5
DOIs
StatePublished - Apr 1 2013

Keywords

  • JAK2 inhibitors
  • Myeloproliferative neoplasms
  • Polycythemia vera
  • Ruxolitinib

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)

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