Hematopoietic Cell Transplantation in the Treatment of Pediatric Acute Myelogenous Leukemia and Myelodysplastic Syndromes: Guidelines from the American Society of Transplantation and Cellular Therapy

Katherine Tarlock, Maria Luisa Sulis, Joseph H. Chewning, Jessica A. Pollard, Todd Cooper, Alan Gamis, Shalini Shenoy, Matthew Kutny, John Horan, Soheil Meshinchi, Jaap Jan Boelens, Marie Bleakley, Paul A. Carpenter, E. Anders Kolb

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

The role of allogeneic hematopoietic stem cell transplantation (HCT) in the treatment of acute myelogenous leukemia (AML) in children is reviewed and critically evaluated in this evidence-based review. Specific criteria were used for searching the published literature, grading the quality and strength of evidence, and assigning the strength of treatment recommendations. Genomic characterization and response to therapy have been critical in the risk stratification of pediatric AML. Although some children are cured with chemotherapy alone, allogeneic HCT offers a survival benefit in selected patients with certain unfavorable risk features and is the standard of care for children who relapse following initial treatment with chemotherapy. Important aspects of HCT include recipient characteristics, donor source, and preparative regimen. The goals of HCT are to reduce incidence of relapse, enhance graft-versus-leukemia (GVL) effects, and minimize graft-versus-host disease. Relapse following HCT remains a significant cause of treatment failure, and interventions pre- and post-HCT, especially those that may augment GVL, are an important focus of ongoing investigations.

Original languageEnglish
Pages (from-to)530-545
Number of pages16
JournalTransplantation and Cellular Therapy
Volume28
Issue number9
DOIs
StatePublished - Sep 2022

Keywords

  • Acute myelogenous leukemia
  • Bone marrow transplantation
  • Chemotherapy
  • Children
  • Cytomolecular
  • Disease status
  • Hematopoietic stem cell transplantation
  • Leukemia risk
  • Measurable residual disease
  • Mutations
  • Pediatric
  • Relapse
  • Therapy

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