Comparison of Hematopoietic Stem Cell Transplantation Results in Patients with β-Thalassemia Major from Three Different Graft Types.
Hematopoietic stem cell transplantation (HSCT)
non-sibling family donor
pediatrics
thalassemia
treosulfan
Journal
Hemoglobin
ISSN: 1532-432X
Titre abrégé: Hemoglobin
Pays: England
ID NLM: 7705865
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
pubmed:
23
1
2021
medline:
18
12
2021
entrez:
22
1
2021
Statut:
ppublish
Résumé
Allogeneic hematopoietic stem cell transplantation (HSCT) is the curative therapy for β-thalassemias that induces severe life-threatening complications. The human leukocyte antigen (HLA) registries and umbilical cord blood banks have carried out diligent searches to find matched unrelated donors (MUDs) for about 70.0% of patients from 2000 onwards. The chance of finding a non-sibling fully matched family donors is higher in some ethnic groups in which consanguineous marriages are common. We have studied and compared transplant complications and outcomes in different graft types (sibling, non-sibling family and unrelated). The non-sibling matched family donor (MFD) group consisted of four mothers, three fathers, five cousins, one paternal uncle and one paternal aunt. There was no significant difference in the mean transfused CD34+ cells, engraftment, median days of neutrophil and platelet recovery were achieved (
Identifiants
pubmed: 33478286
doi: 10.1080/03630269.2021.1872611
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM