High molecular response rate of polycythemia vera patients treated with pegylated interferon alpha-2a.

نویسندگان

  • Jean-Jacques Kiladjian
  • Bruno Cassinat
  • Pascal Turlure
  • Nathalie Cambier
  • Murielle Roussel
  • Sylvia Bellucci
  • Marie-Laurence Menot
  • Gerald Massonnet
  • Jean-Luc Dutel
  • Kamel Ghomari
  • Philippe Rousselot
  • Marie-Jose Grange
  • Yasmina Chait
  • William Vainchenker
  • Nathalie Parquet
  • Lina Abdelkader-Aljassem
  • Jean-François Bernard
  • Jean-Didier Rain
  • Sylvie Chevret
  • Christine Chomienne
  • Pierre Fenaux
چکیده

V617F JAK2 mutation is a reliable molecular marker of polycythemia vera (PV), potentially useful to monitor the effect of treatments in this disease. In a phase 2 study of pegylated (peg) IFN-alpha-2a in PV, we performed prospective sequential quantitative evaluation of the percentage of mutated JAK2 allele (%V617F) by real-time polymerase chain reaction (PCR). The %V617F decreased in 24 (89%) of 27 treated patients, from a mean of 49% to a mean of 27% (mean decrease of 44%; P < .001), and no evidence for a plateau was observed. In one patient, mutant JAK2 was no longer detectable after 12 months. In 3 patients homozygous for the mutation, reappearance of 50% of wild-type allele was observed during treatment. The results seem to confirm the hypothesis that IFN-alpha preferentially targets the malignant clone in PV and show that %V617F assessment using a quantitative method may provide the first tool to monitor minimal residual disease in PV. This trial was registered at www.clinicaltrials.gov as #NCT00241241.

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عنوان ژورنال:
  • Blood

دوره 108 6  شماره 

صفحات  -

تاریخ انتشار 2006