Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia

N Engl J Med. 2009 Jan 29;360(5):470-80. doi: 10.1056/NEJMoa0808253. Epub 2009 Jan 7.

Abstract

Background: Despite best current therapy, up to 20% of pediatric patients with acute lymphoblastic leukemia (ALL) have a relapse. Recent genomewide analyses have identified a high frequency of DNA copy-number abnormalities in ALL, but the prognostic implications of these abnormalities have not been defined.

Methods: We studied a cohort of 221 children with high-risk B-cell-progenitor ALL with the use of single-nucleotide-polymorphism microarrays, transcriptional profiling, and resequencing of samples obtained at diagnosis. Children with known very-high-risk ALL subtypes (i.e., BCR-ABL1-positive ALL, hypodiploid ALL, and ALL in infants) were excluded from this cohort. A copy-number abnormality was identified as a predictor of poor outcome, and it was then tested in an independent validation cohort of 258 patients with B-cell-progenitor ALL.

Results: More than 50 recurring copy-number abnormalities were identified, most commonly involving genes that encode regulators of B-cell development (in 66.8% of patients in the original cohort); PAX5 was involved in 31.7% and IKZF1 in 28.6% of patients. Using copy-number abnormalities, we identified a predictor of poor outcome that was validated in the independent validation cohort. This predictor was strongly associated with alteration of IKZF1, a gene that encodes the lymphoid transcription factor IKAROS. The gene-expression signature of the group of patients with a poor outcome revealed increased expression of hematopoietic stem-cell genes and reduced expression of B-cell-lineage genes, and it was similar to the signature of BCR-ABL1-positive ALL, another high-risk subtype of ALL with a high frequency of IKZF1 deletion.

Conclusions: Genetic alteration of IKZF1 is associated with a very poor outcome in B-cell-progenitor ALL.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • B-Lymphocytes / metabolism
  • Child
  • Cohort Studies
  • DNA Mutational Analysis
  • Drug Resistance, Neoplasm / genetics*
  • Gene Deletion*
  • Gene Expression
  • Gene Expression Profiling
  • Genotype
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • Ikaros Transcription Factor / genetics*
  • Mutation, Missense
  • PAX5 Transcription Factor / genetics
  • Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / drug therapy
  • Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Prognosis
  • Recurrence
  • Trans-Activators / genetics
  • Treatment Outcome

Substances

  • EBF1 protein, human
  • IKZF1 protein, human
  • PAX5 Transcription Factor
  • PAX5 protein, human
  • Trans-Activators
  • Ikaros Transcription Factor