Post-transplantation cyclophosphamide GvHD prophylaxis after hematopoietic stem cell transplantation from 9/10 or 10/10 HLA-matched unrelated donors for acute leukemia
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32409688
DOI
10.1038/s41375-020-0863-4
PII: 10.1038/s41375-020-0863-4
Knihovny.cz E-zdroje
- MeSH
- akutní lymfatická leukemie mortalita patologie terapie MeSH
- akutní myeloidní leukemie mortalita patologie terapie MeSH
- cyklofosfamid terapeutické užití MeSH
- dospělí MeSH
- homologní transplantace MeSH
- imunosupresiva terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- lokální recidiva nádoru mortalita patologie terapie MeSH
- míra přežití MeSH
- mladiství MeSH
- mladý dospělý MeSH
- následné studie MeSH
- nemoc štěpu proti hostiteli farmakoterapie etiologie mortalita patologie MeSH
- nepříbuzný dárce * MeSH
- příprava pacienta k transplantaci MeSH
- prognóza MeSH
- retrospektivní studie MeSH
- senioři MeSH
- testování histokompatibility MeSH
- transplantace hematopoetických kmenových buněk škodlivé účinky 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
- cyklofosfamid MeSH
- imunosupresiva MeSH
HLA-matching largely contributes to unrelated donor hematopoietic cell transplantation (UD-HCT) success but, due to the selective deletion of alloreactive T-cells, post-transplantation cyclophosphamide (PTCy) could modulate its negative impact on outcomes. We retrospectively compared acute leukemia patients receiving 10/10 or 9/10 HLA allele-matched UD-HCT with PTCy-GvHD prophylaxis between 2010 and 2017, reported to EBMT registry. The 100-day incidence of grade ≥2 and grade ≥3 aGvHD were comparable for 10/10 and 9/10 UD (28% versus 28%, p = 0.8 and 10% versus 8%, p = 0.5, respectively). The 2-year cGvHD and extensive cGvHD were similar between 10/10 and 9/10 UD (35% versus 44%, p = 0.2 and 21% versus 20%, p = 0.6, respectively). The 2-year nonrelapse mortality was 20% after 10/10 and 16% after 9/10 UD-HCT (p = 0.1). Relapse incidence at 2-year was 24% for 10/10 and 28% for 9/10 UD-HCT (p = 0.4). Leukemia-free survival at 2-year was the same for 10/10 and 9/10 UD (56 and 56%, p = 0.6, respectively), with comparable overall survival (62 and 59%, p = 0.9, respectively). Multivariate analysis showed no effect of HLA-matching on outcomes. An advanced disease status and patient disability remained the most important factors portending a worse survival. PTCy could alleviate the detrimental effect of HLA-allele mismatching in UD-HCT, potentially expanding the donor pool for acute leukemia patients.
Acute Leukemia Working Party of EBMT Paris France
Asklepios Klinik St George Lohmühlenstrasse Hamburg Germany
Cellular Therapy and Immunobiology Working Party Marseille France
Centre d'Investigations Cliniques en Biothérapies Institut Paoli Calmette Marseille Marseille France
Department of Hematology University Medical Center Amsterdam Netherlands
Department of Pediatric Hematology and Oncology IRCCS Bambino Gesù Children's Hospital Rome Italy
Department of Stem cell Transplantation University Hospital Eppendorf Hamburg Germany
Erasmus MC Daniel den Hoed Cancer Centre Rotterdam Netherlands
German Cancer Consortium Heidelberg Germany
Hematology and Bone Marrow Transplantation Unit IRCCS San Raffaele Scientific Institute Milano Italy
Hôpital Saint Antoine Paris University UPMC INSERM U938 Paris France
Hospital Clinic Institute of Hematology and Oncology Barcelona Spain
Institute for Experimental Cellular Therapy Essen University Hospital Essen Germany
Institute of Hematology and Blood Transfusion Prague Czech Republic
Service d'Hématologie Clinique et Thérapie Cellulaire Hôpital Saint Antoine AP HP Paris France
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