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High-vs low-dose cytarabine combined with interferon alfa in patients with first chronic phase chronic myeloid leukemia. A prospective randomized phase III study

  • W. Deenik
  • , B. van der Holt
  • , G. E.G. Verhoef
  • , A. V.M.B. Schattenberg
  • , L. F. Verdonck
  • , S. M.G.J. Daenen
  • , P. Zachée
  • , P. H.M. Westveer
  • , W. M. Smit
  • , S. Wittebol
  • , H. C. Schouten
  • , B. Löwenberg
  • , G. J. Ossenkoppele
  • , J. J. Cornelissen*
  • *Corresponding author for this work
  • University Hospitals Leuven
  • Radboud University Medical Center
  • Utrecht University
  • University Medical Centre Groningen
  • Antwerp University Hospital
  • Meander Medical Center
  • VU University Medical Center
  • HOVON Data Center
  • University Hospital of Maastricht

Research output: Contribution to journalArticleAcademicpeer-review

8 Citations (Scopus)

Abstract

A prospective randomized phase III study was performed to evaluate whether intensified cytarabine would induce a higher response rate and longer event-free interval as compared to low-dose cytarabine in chronic myeloid leukemia (CML). One hundred and eighteen patients with CML in early chronic phase entered the study. Twenty-eight out of 32 patients assigned to group A received two cycles of a combination of intensified cytarabine and idarubicin followed by interferon alfa (IFN-α) maintenance, 28 patients in group B received standard treatment by a combination of low-dose cytarabine and IFN-α. Forty-nine patients with a human leukocyte antigen-identical sibling donor proceeded to allogeneic stem cell transplantation (allo-SCT) and nine patients were excluded from the analysis. Hematological response was observed in 97% of the patients in group A vs 86% of the patients in group B during the first year of treatment. In group A, 16 patients (50%) achieved a major cytogenetic response, which compared to seven patients (25%) with a major cytogenetic response in group B. With a median follow-up of 58 months (range 34-76), event-free survival was not significantly different between arms A and B. The estimated 5-year survival rate was 56% in the intensified arm and 77% in the low-dose arm (P=0.05). Recipients of allo-SCT showed a 5-year estimated survival rate of 55%. Although intensified cytarabine induced a higher initial percentage of major and complete cytogenetic responses, responses were not sustained by IFN-α maintenance therapy.

Original languageEnglish
Pages (from-to)117-125
Number of pages9
JournalAnnals of Hematology
Volume86
Issue number2
DOIs
Publication statusPublished - 10 Oct 2006

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