Rearrangement in the breakpoint cluster region and the clinical course in Philadelphia-negative chronic myelogenous leukemia

Ann Intern Med. 1986 Nov;105(5):673-9. doi: 10.7326/0003-4819-105-5-673.

Abstract

We have followed one patient with Philadelphia (Ph)-negative chronic myelogenous leukemia and identified an additional four patients from the literature who showed the rearrangement in the breakpoint cluster region (bcr) on chromosome 22 characteristic of Ph-positive chronic myelogenous leukemia. The clinical course of these five patients was similar to that of Ph-positive patients, with easily controlled leukocyte counts, a prolonged benign phase, and prolonged survival. Furthermore, we have shown, for the first time, that bcr rearrangement in Ph-negative chronic myelogenous leukemia can result in expression of the aberrant 210-kilodalton bcr-abl fusion protein, which has been strongly implicated in Ph-positive leukemogenesis. Research data pertaining to possible cytogenetic mechanisms leading to production of p210bcr-abl in the absence of the Ph chromosome are reviewed. Molecular analysis provides an important tool for classifying and predicting prognosis of some patients with Ph-negative chronic myelogenous leukemia.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Human, Pair 11 / ultrastructure*
  • Chromosomes, Human, Pair 22 / ultrastructure*
  • Chromosomes, Human, Pair 9 / ultrastructure*
  • Fusion Proteins, bcr-abl
  • Humans
  • Leukemia, Myeloid / genetics*
  • Leukemia, Myeloid, Acute / genetics
  • Male
  • Middle Aged
  • Oncogenes
  • Philadelphia Chromosome
  • Protein-Tyrosine Kinases / genetics
  • Recombinant Fusion Proteins / genetics
  • Translocation, Genetic*

Substances

  • Recombinant Fusion Proteins
  • Protein-Tyrosine Kinases
  • Fusion Proteins, bcr-abl