Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia

Anthony V. Moorman, Sue M. Richards, Mary Martineau, Kan Luk Cheung, Hazel M. Robinson, G. Reza Jalali, Zoë J. Broadfield, Rachel L. Harris, Kerry E. Taylor, Brenda E.S. Gibson, Ian M. Hann, Frank G.H. Hill, Sally E. Kinsey, Tim O.B. Eden, Christopher D. Mitchell, Christine J. Harrison

Research output: Contribution to journalArticlepeer-review

Abstract

High hyperdiploidy (HeH) (51 to 65 chromosomes) is found in one third of children with acute lymphoblastic leukemia and is associated with a good prognosis. Cytogenetic features may further refine this prognosis and identify patients with a poor outcome. We examined the effect of sex, age, individual trisomies, modal number, and structural abnormalities on survival among 700 children with HeH. Univariate analysis showed that age. sex, +4, +10, +18, and a high modal number were associated with survival. Multivariate analysis however, revealed that only age, sex, +4, and +18 were independent indicators. Hazard scores for predicting relapse and mortality were constructed. Three risk groups with 5-year event-free survival (EFS) rates of 86%, 75%, and 50% (P < .0001) were identified. The high-risk group comprised boys older than 9 years, boys aged 1 through 9 years without +18, and girls older than 9 years without +18, while girls aged 1 through 9 years with +18 had the best EFS. In terms of mortality, those younger than age 10 years with both +4 and +18 had an improved survival (96% vs 84% at 5 years, P < .0001). These findings confirm that the outcome of children with HeH is heterogeneous and that specific trisomies can identify patients with the greatest and least risk of treatment failure.

Original languageEnglish (US)
Pages (from-to)2756-2762
Number of pages7
JournalBlood
Volume102
Issue number8
DOIs
StatePublished - Oct 15 2003
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

Fingerprint Dive into the research topics of 'Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia'. Together they form a unique fingerprint.

Cite this