Deletion of <i>IKZF1</i> and Prognosis in Acute Lymphoblastic Leukemia

Charles G. Mullighan(St. Jude Children's Research Hospital), Xiaoping Su, Jinghui Zhang(Center for Information Technology), Ina Radtke, Letha A. Phillips, Christopher B. Miller, Jing Ma, Wei Liu, Cheng Cheng, Brenda A. Schulman(National Institutes of Health), Richard C. Harvey(New Mexico Cancer Center), I‐Ming Chen(University of New Mexico), Robert Clifford(Laboratory of Molecular Genetics), William L. Carroll(New York University), Gregory H. Reaman(Children's National), W. Paul Bowman(Cook Children's Medical Center), Meenakshi Devidas(Children's Oncology Group), Daniela S. Gerhard(Office of Public Health Genomics), Wenjian Yang, Mary V. Relling, Sheila Shurtleff, Dario Campana(St. Jude Children's Research Hospital), Michael J. Borowitz, Ching‐Hon Pui(St. Jude Children's Research Hospital), Malcolm A. Smith, Stephen P. Hunger(Children's Hospital Colorado), Cheryl L. Willman(University of New Mexico), James R. Downing
New England Journal of Medicine
January 7, 2009
Cited by 1,442Open Access
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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.


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