Post-transplantation cyclophosphamide and antithymocyte globulin in 8/10 HLA-mismatched unrelated donor transplantation: the analysis on behalf of the transplant complications working party of the EBMT
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
40830235
DOI
10.1038/s41409-025-02678-z
PII: 10.1038/s41409-025-02678-z
Knihovny.cz E-zdroje
- MeSH
- antilymfocytární sérum * terapeutické užití farmakologie aplikace a dávkování MeSH
- cyklofosfamid * terapeutické užití farmakologie MeSH
- dospělí MeSH
- hematologické nádory terapie mortalita MeSH
- HLA antigeny MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- nemoc štěpu proti hostiteli * prevence a kontrola mortalita MeSH
- nepříbuzný dárce * MeSH
- příprava pacienta k transplantaci * metody MeSH
- registrace MeSH
- senioři MeSH
- transplantace hematopoetických kmenových buněk * metody MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antilymfocytární sérum * MeSH
- cyklofosfamid * MeSH
- HLA antigeny MeSH
Allogeneic hematopoietic cell transplantation (alloHCT) from 8/10 HLA-matched unrelated donor is performed in a minority of patients. There is little data on its outcomes and consequently, guidelines on optimal transplantation procedures are lacking. The Transplant complications working party of the EBMT performed a registry study comparing approaches to graft-versus-host disease (GVHD) prophylaxis in recipients of alloHCT from 8/10 HLA-mismatched unrelated donors (8/10 MMUD). The analysis included 450 adult patients with hematological malignancies receiving a first alloHCT between 2015 and 2021, GVHD prophylaxis strategies included ATG in 318 and PTCy in 132 patients. AlloHCT from 8/10 MMUD resulted in 21.1% non-relapse mortality, 28.5% cumulative incidence of relapse, 55.7% overall survival (OS), 50.4% progression-free-survival and 39.8% GVHD-relapse-free survival (GRFS). PTCy decreased the risk of grade II-IV (HR 0.63, 95%CI 0.40-0.99) and III-IV acute GVHD (HR 0.31, 95%CI 0.13-0.74), improved OS (HR 0.63, 95%CI 0.41-0.95) and GRFS (HR 0.65, 95%CI 0.47-0.91). No other differences between the groups were documented. Transplantation from female donors to male recipients increased the incidence of extensive chronic GVHD (HR 2.39, 95%CI 1.10-5.19) and decreased PFS (HR 1.49, 95%CI 1.01-2.20). AlloHCT from 8/10 HLA-matched unrelated donor is feasible and the use of PTCy in GVHD prophylaxis improves outcomes.
Comprehensive Cancer Center Faculty of Life Sciences and Medicine King's College London London UK
Department of Hematology Rijeka University Hospital Centre Rijeka Croatia
Essen University Hospital Essen Germany
Hannover Medical School Hannover Germany
Institute of Hematology and Blood Transfusion Prague Czech Republic
Ospedale Infantile Regina Margherita Torino Italy
Ospedale San Gerardo Monza Italy
Programme de Transplantation and Therapie Cellulaire Marseille France
RM Gorbacheva Research Institute Pavlov University St Petersburg Russia
S S C 5 D Trapianto di Cellule Staminali Torino Italy
Saint Louis Hospital BMT Unit Paris France
Tor Vergata University of Rome Rome Italy
Transplant Complications Working Party of EBMT Paris France
Universitaet Tuebingen Tuebingen Germany
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