Assessment of chimerism and immunomodulation to prevent post-transplantation relapse in childhood acute myeloblastic leukemia: is it the right approach?

Pediatr Hematol Oncol. 2020 Apr;37(3):259-268. doi: 10.1080/08880018.2020.1717697. Epub 2020 Feb 6.

Abstract

Relapse of acute myeloblastic leukemia (AML) after first allogenic hematopoietic stem-cell transplantation (allo-HSCT) is a fatal complication. Sixty-five children transplanted for AML were included in a prospective national study from June 2005 to July 2008 to explore the feasibility of preemptive immune modulation based on the monitoring of blood chimerism. Relapse occurred in 23 patients (35%). The median time between the last complete chimerism and relapse was 13.5 days (2-138). Prompt discontinuation of cyclosporin and the administration of donor lymphocyte infusions (DLIs) based on chimerism monitoring failed as a preemptive tool, either for detecting relapse or certifying long-term remission.

Keywords: Acute myeloid leukemia; chimerism; donor lymphocyte infusions; immunotherapy; relapse of acute myeloblastic leukemia; stem cell transplantation.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Video-Audio Media

MeSH terms

  • Allografts
  • Child
  • Cyclosporine / administration & dosage*
  • Cyclosporine / adverse effects
  • Female
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Immunomodulation*
  • Leukemia, Myeloid, Acute* / blood
  • Leukemia, Myeloid, Acute* / prevention & control
  • Lymphocyte Transfusion*
  • Male
  • Prospective Studies
  • Recurrence
  • Tissue Donors*
  • Transplantation Chimera / blood*

Substances

  • Cyclosporine