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

B Benjamin J. Huang (2Division of Oncology, Department of Pediatrics, University of California San Francisco, San Francisco, CA) L Lauren K. Meyer T Todd A. Alonzo (Univ. of Southern California Keck School of Medicine, Los Angeles, CA) Y Yi-Cheng Wang A Adam J. Lamble R Rhonda E. Ries W Weijie Wang B Betsy Hirsch (7University of Minnesota Cancer Center, Minneapolis, United States) G Gordana Raca (8Children's Hospital Los Angeles, Los Angeles, United States) X Xiaotu Ma (1Department of Computational Biology, St. Jude Children’s Research Hospital, Memphis, TN) A Alan S. Gamis R Richard Aplenc E E. Anders Kolb T Todd M. Cooper (25Cancer and Blood Disorders Center, Seattle Children’s Hospital, Seattle, WA) K Katherine Tarlock (3Seattle Children's Hospital, Division of Hematology and Oncology, Seattle, United States) M Michael R. Loken (Hematologics, Inc, Seattle, WA) S Soheil Meshinchi J Joseph H. Chewning (12Division of Pediatric Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL) W William G. Woods J John T. Horan

Abstract

PURPOSE Hematopoietic 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. METHODS We 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. RESULTS Our 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. CONCLUSION HSCT was associated with improved outcomes in pediatric patients with contemporarily defined high-risk AML.

Article Details

Volume / Issue Vol. 43, Issue 17
Published June 10, 2025
Pages 1961-1971
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

B

Benjamin J. Huang

2Division of Oncology, Department of Pediatrics, University of California San Francisco, San Francisco, CA

L

Lauren K. Meyer

T

Todd A. Alonzo

Univ. of Southern California Keck School of Medicine, Los Angeles, CA

Y

Yi-Cheng Wang

A

Adam J. Lamble

R

Rhonda E. Ries

W

Weijie Wang

B

Betsy Hirsch

7University of Minnesota Cancer Center, Minneapolis, United States

G

Gordana Raca

8Children's Hospital Los Angeles, Los Angeles, United States

X

Xiaotu Ma

1Department of Computational Biology, St. Jude Children’s Research Hospital, Memphis, TN

A

Alan S. Gamis

R

Richard Aplenc

E

E. Anders Kolb

T

Todd M. Cooper

25Cancer and Blood Disorders Center, Seattle Children’s Hospital, Seattle, WA

K

Katherine Tarlock

3Seattle Children's Hospital, Division of Hematology and Oncology, Seattle, United States

M

Michael R. Loken

Hematologics, Inc, Seattle, WA

S

Soheil Meshinchi

J

Joseph H. Chewning

12Division of Pediatric Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL

W

William G. Woods

J

John T. Horan