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Hematopoietic Stem Cell Transplantation Outcomes for High-Risk AML: A Report From the Children's Oncology Group

  • Benjamin J. Huang
  • , Lauren K. Meyer
  • , Todd A. Alonzo
  • , Yi Cheng Wang
  • , Adam J. Lamble
  • , Rhonda E. Ries
  • , Weijie Wang
  • , Betsy Hirsch
  • , Gordana Raca
  • , Xiaotu Ma
  • , Alan S. Gamis
  • , Richard Aplenc
  • , E. Anders Kolb
  • , Todd M. Cooper
  • , Katherine Tarlock
  • , Michael R. Loken
  • , Soheil Meshinchi
  • , Joseph H. Chewning
  • , William G. Woods
  • , John T. Horan

Research output: Contribution to journalArticlepeer-review

Abstract

PURPOSEHematopoietic stem cell transplantation (HSCT) is used as consolidation for pediatric patients with high-risk AML in first complete remission (CR1). The definition of high-risk AML has evolved considerably over the past two decades with the successive identification of new unfavorable risk factors. We conducted a cross-study analysis to determine whether HSCT improves the outcomes of patients with contemporarily defined high-risk AML.METHODSWe combined data from AAML0531 and AAML1031, the last two phase III clinical trials completed by the Children's Oncology Group (COG). These two trials established the prognostic importance of measurable residual disease (MRD) and several high-risk cryptic cytogenetic/molecular (CM) alterations, which were applied to reclassify patients in the current COG phase III clinical trial, AAML1831. We compared the outcomes after HSCT in CR1 with those after chemotherapy alone in CR1 in the redefined high-risk group.RESULTSOur study cohort comprised 463 patients with high-risk CM alterations and 72 patients with standard-risk (SR) CM results with positive MRD at end of induction I. In all, 33.9% and 45.8% of these groups underwent HSCT in CR1, respectively. HSCT was associated with decreased relapse and improved disease-free survival (DFS) in both groups. In the high-risk CM group, 5-year DFS was 26.0% (95% CI, 20.6 to 31.6) and 49.8% (95% CI, 41.7 to 57.4; P <.001) in patients receiving chemotherapy alone and HSCT, respectively. In the SR CM and MRD+ groups, DFS was 16.9% (95% CI, 4.3 to 36.7) compared with 50.9% (95% CI, 32.7 to 66.5; P =.032). HSCT was also associated with improvement in outcomes based on multivariable analysis and across subgroups defined by clinical trial and by high-risk CM subtype, with the exception of chromosome 7 or 5 loss.CONCLUSIONHSCT was associated with improved outcomes in pediatric patients with contemporarily defined high-risk AML.

Original languageEnglish (US)
Pages (from-to)1961-1971
Number of pages11
JournalJournal of Clinical Oncology
Volume43
Issue number17
DOIs
StatePublished - Jun 10 2025

Bibliographical note

Publisher Copyright:
© 2025 by American Society of Clinical Oncology.

PubMed: MeSH publication types

  • Journal Article
  • Clinical Trial, Phase III
  • Research Support, N.I.H., Extramural

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