Modulation of JAK2 V617F allele burden dynamics by hydroxycarbamide in polycythaemia vera and essential thrombocythaemia patients

Br J Haematol. 2011 Feb;152(4):413-9. doi: 10.1111/j.1365-2141.2010.08467.x. Epub 2011 Jan 10.

Abstract

The modulation of JAK2 V617F allele burden dynamics was prospectively analysed in 47 patients (26 polycythaemia vera [PV] and 21 essential thrombocythaemia [ET]) treated with first-line hydroxyurea (HU) and compared with the JAK2 V617F dynamics of a control group of 45 PV and ET patients. A partial molecular response (PMR), according to European Leukaemia Net criteria, was observed in 27/47 (57%) patients. Median time to PMR was 14 months (3-66) with a probability of PMR at 3 years of 57%. A significant decrease in JAK2 V617F allele load was observed at 36 months both in PV and ET patients, being the reduction in PV higher than in ET patients (P = 0·01). A haematocrit ≥0·45 L/L was associated with a higher probability of attaining a PMR (HR:3·4; 95%CI:1·02-11·6, P = 0·04). Control group showed a slight increase of JAK2 V617F allele burden over time. The reduction in the mutated allele load comparing treated patients versus controls was highly significant both in PV and ET, demonstrating a clear effect of HU on the JAK2 V617F allele burden. In conclusion, first-line HU can attain PMR in more than 50% of newly diagnosed PV and ET patients, with a continuous decrease of the JAK2 V617F allele burden in PV patients during treatment.

Publication types

  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • Female
  • Follow-Up Studies
  • Genetic Load
  • Humans
  • Hydroxyurea / pharmacology*
  • Hydroxyurea / therapeutic use
  • Janus Kinase 2 / genetics*
  • Male
  • Middle Aged
  • Nucleic Acid Synthesis Inhibitors / pharmacology*
  • Nucleic Acid Synthesis Inhibitors / therapeutic use
  • Polycythemia Vera / drug therapy
  • Polycythemia Vera / genetics*
  • Prospective Studies
  • Thrombocythemia, Essential / drug therapy
  • Thrombocythemia, Essential / genetics*
  • Treatment Outcome

Substances

  • Nucleic Acid Synthesis Inhibitors
  • JAK2 protein, human
  • Janus Kinase 2
  • Hydroxyurea