Assessment of minimal residual disease in acute promyelocytic leukaemia with t(15;17) by chromosome painting

Eur J Haematol. 1995 Jul;55(1):10-3. doi: 10.1111/j.1600-0609.1995.tb00226.x.

Abstract

To detect the minimal residual disease (MRD) in acute promyelocytic leukaemia patients treated with all-trans retinoic acid, we compared the sensitivity of metaphase fluorescence in situ hybridization (FISH) with conventional analysis of G-banded metaphases. 5 out of 6 patients studied at diagnosis showed the t(15;17) translocation. 4 out of 5 patients carrying t(15;17) achieved complete remission and conventional cytogenetic conversion. In 3 cases the whole chromosome painting (WCP) probe 17 discovered one normal chromosome 17 and two fragments indicative of t(15;17) persistence. The FISH-WCP technique seems to be highly sensitive and recommendable in monitoring leukaemias with specific chromosome rearrangements.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Chromosome Banding
  • Chromosomes, Human, Pair 17 / genetics
  • Female
  • Humans
  • In Situ Hybridization
  • Leukemia, Promyelocytic, Acute / diagnosis*
  • Leukemia, Promyelocytic, Acute / drug therapy
  • Leukemia, Promyelocytic, Acute / genetics
  • Male
  • Middle Aged
  • Neoplasm, Residual
  • Translocation, Genetic
  • Tretinoin / therapeutic use

Substances

  • Tretinoin