Prognostic significance of myeloperoxidase expression in childhood acute myeloid leukemia

Pediatr Blood Cancer. 2008 Mar;50(3):542-8. doi: 10.1002/pbc.21258.

Abstract

Background: The percentage of myeloperoxidase (MPO)-positive blast cells is associated with prognosis in adult acute myeloid leukemia (AML), but this association is unsubstantiated in pediatric AML.

Procedure: We retrospectively compared cytochemical MPO results with outcome in 154 patients younger than 21 years treated on three consecutive institutional protocols for newly diagnosed AML (1987-2001). Patients with FAB M0 and M7 AML (no MPO expression) or M3 AML (100% MPO expression) and Down's syndrome were excluded.

Results: Median MPO expression was higher in FAB M2 subtype than in other subtypes (P < 0.0001) and differed significantly across cytogenetic risk groups (P = 0.002) with highest MPO expression among those with favorable karyotypes. The percentage of MPO-positive blasts was not significantly associated with the probability of complete remission (P = 0.97), event-free survival (P = 0.72), or survival (P = 0.76) in multivariate analyses that accounted for age, FAB subtype, presenting WBC count, cytogenetic and protocol treatment risk group. In analysis limited to patients with intermediate-risk cytogenetics, higher MPO expression appeared to be associated with improved EFS (P = 0.06) but was not associated with remission induction rate (P = 0.16) or overall survival (P = 0.38).

Conclusions: The percentage of MPO-positive blast cells is related to FAB subtype in pediatric AML but has limited prognostic relevance.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Biomarkers
  • Child
  • Child, Preschool
  • Disease-Free Survival
  • Female
  • Humans
  • Infant
  • Kaplan-Meier Estimate
  • Karyotyping
  • Leukemia, Myeloid / blood*
  • Leukemia, Myeloid / classification
  • Leukemia, Myeloid / genetics
  • Leukemia, Myeloid / mortality
  • Male
  • Myeloid Cells / enzymology*
  • Neoplastic Stem Cells / enzymology*
  • Peroxidase / blood*
  • Prognosis
  • Retrospective Studies
  • Risk
  • Survival Analysis

Substances

  • Biomarkers
  • Peroxidase