Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia

E Waanders, V H J van der Velden, C E van der Schoot, F N van Leeuwen, S V van Reijmersdal, V de Haas, A J Veerman, A Geurts van Kessel, P M Hoogerbrugge, R. Kuiper, J J M van Dongen

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Response to therapy as determined by minimal residual disease (MRD) is currently used for stratification in treatment protocols for pediatric acute lymphoblastic leukemia (ALL). However, the large MRD-based medium risk group (MRD-M; 50-60% of the patients) harbors many relapses. We analyzed MRD in 131 uniformly treated precursor-B-ALL patients and evaluated whether combined MRD and IKZF1 (Ikaros zinc finger-1) alteration status can improve risk stratification. We confirmed the strong prognostic significance of MRD classification, which was independent of IKZF1 alterations. Notably, 8 of the 11 relapsed cases in the large MRD-M group (n=81; 62%) harbored an IKZF1 alteration. Integration of both MRD and IKZF1 status resulted in a favorable outcome group (n=104; 5 relapses) and a poor outcome group (n=27; 19 relapses), and showed a stronger prognostic value than each of the established risk factors alone (hazard ratio (95%CI): 24.98 (8.29-75.31)). Importantly, whereas MRD and IKZF1 status alone identified only 46 and 54% of the relapses, respectively, their integrated use allowed prediction of 79% of all the relapses with 93% specificity. Because of the unprecedented sensitivity in upfront relapse prediction, the combined parameters have high potential for future risk stratification, particularly for patients originally classified as non-high risk, such as the large group of MRD-M patients.

Original languageEnglish
Pages (from-to)254-8
Number of pages5
JournalLeukemia
Volume25
Issue number2
DOIs
Publication statusPublished - Feb 2011
Externally publishedYes

Keywords

  • Child
  • Gene Rearrangement
  • Humans
  • Ikaros Transcription Factor/genetics
  • Kaplan-Meier Estimate
  • Mutation
  • Neoplasm, Residual/pathology
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma/mortality
  • Predictive Value of Tests
  • Recurrence
  • Risk Assessment
  • Sensitivity and Specificity

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