Durable engraftment and correction of hematological abnormalities in children with congenital amegakaryocytic thrombocytopenia following myeloablative umbilical cord blood transplantation

Pediatr Transplant. 2015 Nov;19(7):753-7. doi: 10.1111/petr.12577. Epub 2015 Sep 14.

Abstract

The use of HSCT is the only potentially curative treatment for CAMT, but access is limited by the availability of suitable donors. We report five consecutive patients with CAMT who received MAC and partially HLA-mismatched, UCBT (unrelated, n = 4). Median times to neutrophil (>500/μL) and platelet (≥20 000 and ≥50 000/μL) engraftment were 19, 57, and 70 days, respectively. Acute GvHD, grade II, developed in one patient, who subsequently developed limited chronic GvHD. At median follow-up of 14 yr, all patients are alive with sustained donor cell engraftment. To our knowledge, this is the largest single-center series of UCBT for patients with this disease and suggests that UCBT is a successful curative option for patients with CAMT.

Keywords: congenital amegakaryocytic thrombocytopenia; cord blood transplantation; hematopoietic stem cell transplantation; thrombocytopenia.

Publication types

  • Clinical Trial

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Congenital Bone Marrow Failure Syndromes
  • Cord Blood Stem Cell Transplantation*
  • Female
  • Follow-Up Studies
  • Graft vs Host Disease
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Thrombocytopenia / blood
  • Thrombocytopenia / therapy*
  • Transplantation Conditioning*
  • Treatment Outcome

Supplementary concepts

  • Congenital amegakaryocytic thrombocytopenia