CD34+ selected peripheral blood Stem Cell Boost (SCB) for Poor Graft Function (PGF) or mixed chimerism in pediatric patients, after hematopoietic stem cell transplantation: Results of a retrospective multicenter study

Pediatr Transplant. 2021 Aug;25(5):e13909. doi: 10.1111/petr.13909. Epub 2020 Nov 3.

Abstract

Background: PGF is historically associated with high morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT).

Methods: In this study, we report our multicenter experience on stem cell boost (SCB) for PGF, or incomplete donor engraftment, in 16 pediatric patients. Donors were HLA-matched siblings (n = 4), unrelated donors (n = 11), or haploidentical family members (n = 1). Ten patients had two-lineage cytopenia, 5 had one-lineage cytopenia, and 1 had poor immunological reconstitution together with a low percentage of donor cell engraftment. A median of 6.6x106 selected CD34+/Kg was infused after 194 days from allo-HSCT (48-607).

Results: In 4 out of 5 patients, one-lineage cytopenia was resolved, while among the 10 patients with two-lineage cytopenia, 4 resolved both cytopenia, 5 resolved one-lineage, and one did not respond. All patients reverted their mixed chimera to full donor chimera. OS was 56%, transplant-related mortality (TRM) 32%, and RI 12%. The main causes of failure were related to infections with 4 out of 7 deaths caused by this.

Conclusions: SCB may rescue over 50% of patients with PGF after allo-HSCT. An earlier treatment may reduce the infectious complications and improve survival.

Keywords: pediatric patients; stem cell boost.

Publication types

  • Multicenter Study

MeSH terms

  • Adolescent
  • Antigens, CD34 / immunology*
  • Child
  • Child, Preschool
  • Chimerism*
  • Female
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Infant
  • Italy
  • Leukemia / immunology*
  • Leukemia / therapy*
  • Leukopenia / immunology*
  • Leukopenia / therapy*
  • Male
  • Retrospective Studies
  • Transplantation Conditioning

Substances

  • Antigens, CD34