N-ras mutation in acute myeloid leukemia: incidence, prognostic significance and value as a marker of minimal residual disease

Pathology. 1993 Jan;25(1):57-62. doi: 10.3109/00313029309068903.

Abstract

The polymerase chain reaction (PCR) and allele specific oligonucleotide (ASO) hybridization have been used to investigate the incidence of N-ras mutation in acute myeloid leukemia (AML). The prognostic significance of these mutations and their value as markers of minimal residual disease have also been assessed. Mutated N-ras alleles were detected in 9 of 69 AML patients (13%). No significant difference in survival or remission duration was found between those patients with an N-ras mutation and those without. Four patients with N-ras mutations at presentation were followed through disease progression. The results showed no consistent pattern of association between the presence of an N-ras mutation and disease state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Female
  • Genes, ras / genetics*
  • Genetic Markers
  • Humans
  • Incidence
  • Leukemia, Myeloid, Acute / drug therapy
  • Leukemia, Myeloid, Acute / epidemiology
  • Leukemia, Myeloid, Acute / genetics*
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Prognosis
  • Recurrence
  • Remission Induction
  • Retrospective Studies

Substances

  • Genetic Markers