Post-transplantation cyclophosphamide-based haploidentical versus Atg-based unrelated donor allogeneic stem cell transplantation for patients younger than 60 years with hematological malignancies: a single-center experience of 209 patients.
Acute Disease
Adult
Allografts
Antilymphocyte Serum
/ administration & dosage
Chronic Disease
Cyclophosphamide
/ administration & dosage
Disease-Free Survival
Female
Graft vs Host Disease
/ etiology
Hematologic Neoplasms
/ mortality
Hematopoietic Stem Cell Transplantation
Humans
Incidence
Male
Middle Aged
Survival Rate
Unrelated Donors
Journal
Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
10
08
2018
accepted:
20
10
2018
revised:
10
10
2018
pubmed:
8
11
2018
medline:
29
7
2020
entrez:
8
11
2018
Statut:
ppublish
Résumé
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is limited by availability of HLA-matched sibling donors (MSDs). The alternative use of unrelated donors (UDs) is currently challenged by haploidentical-related donors (HRDs). We retrospectively analyzed 209 consecutive patients younger than 60 years undergoing allo-HSCT from UDs (n = 128) or HRDs (n = 81). Cumulative incidences of grade 3-4 acute (17 vs. 2%, p = 0.003) and 2-year moderate and severe chronic (20 vs. 2%, p < 0.001) GVHD were significantly higher with UD. Progression-free survival (PFS) was significantly better with HRD (51 vs. 69%, p = 0.019), without significant difference in the cumulative incidence of relapse (CIR), non-relapse mortality (NRM), and overall survival (OS). Multivariate analyses confirmed the lower risk of acute and chronic GVHD (grade 2-4, HR = 0.43, p = 0.005; grade 3-4, HR = 0.20, p = 0.017; all grades, HR = 0.43, p = 0.012; moderate or severe, HR = 0.12, p = 0.004), better PFS (HR = 0.61, p = 0.046), and GRFS (HR = 0.47, p = 0.001) with HRD. This was confirmed in match-paired analysis. In the absence of MSDs, HRD could be considered as a suitable alternative for patients younger than 60 years.
Identifiants
pubmed: 30401970
doi: 10.1038/s41409-018-0387-y
pii: 10.1038/s41409-018-0387-y
doi:
Substances chimiques
Antilymphocyte Serum
0
Cyclophosphamide
8N3DW7272P
Types de publication
Clinical Trial
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM