Solid organ transplantation after hematopoietic stem cell transplantation in childhood: A multicentric retrospective survey
Language English Country United States Media print-electronic
Document type Journal Article, Multicenter Study
PubMed
30586230
DOI
10.1111/ajt.15240
PII: S1600-6135(22)09124-9
Knihovny.cz E-resources
- Keywords
- bone marrow/hematopoietic stem cell transplantation, clinical research/practice, graft-vs-host disease (GVHD), heart failure/injury, kidney failure/injury, liver disease, lung (allograft) function/dysfunction, organ transplantation in general, pediatrics,
- MeSH
- Allografts MeSH
- Autografts MeSH
- Child MeSH
- Cohort Studies MeSH
- Infant MeSH
- Humans MeSH
- Survival Rate MeSH
- Adolescent MeSH
- Graft vs Host Disease etiology surgery MeSH
- Child, Preschool MeSH
- Proportional Hazards Models MeSH
- Surveys and Questionnaires MeSH
- Retrospective Studies MeSH
- Hematopoietic Stem Cell Transplantation adverse effects MeSH
- Liver Transplantation MeSH
- Kidney Transplantation MeSH
- Organ Transplantation * adverse effects mortality MeSH
- Lung Transplantation MeSH
- Heart Transplantation MeSH
- Treatment Outcome MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Geographicals
- Europe epidemiology MeSH
We report data obtained from a retrospective multicenter pediatric survey on behalf of the European Society for Blood and Marrow Transplantation (EBMT). Information on solid organ transplantation (SOT) performed in pediatric recipients of either autologous or allogeneic hematopoietic stem cell transplantation (HSCT) between 1984 and 2016 was collected in 20 pediatric EBMT Centers (25.6%). Overall, we evaluated data on 44 SOTs following HSCT including 20 liver (LTx), 12 lung (LuTx), 6 heart (HTx), and 6 kidney (KTx) transplantations. The indication for SOT was organ failure related to intractable graft-vs-host disease in 16 children (36.3%), acute or chronic HSCT-related toxicity in 18 (40.9%), and organ dysfunction related to the underlying disease in 10 (22.8%). The median follow-up was 10.9 years (95% confidence interval: 1.7-29.5). The overall survival rate at 1 and 5 years after SOT was 85.7% and 80.4%, respectively: it was 74% and 63.2% after LTx, 83.2% after HTx, and 100% equally after LuTx and KTx. This multicenter survey confirms that SOT represents a promising option in children with severe organ failure occurring after HSCT. Additional studies are needed to further establish the effectiveness of SOT after HSCT and to better understand the mechanism underlying this encouraging success.
Department of Pediatric Oncology and Hematology Hospital Universitario Vall d'Hebron Barcelona Spain
Department of Pediatrics Jena University Hospital Jena Germany
Department of Pediatrics University Medical Center Ulm Germany
Department Pediatric Hematology Oncology Hemostaseology Universitätsklinikum Leipzig Leipzig Germany
Dipartimento di Onco Ematologia Pediatrica IRCSS Ospedale Pediatrico Bambino Gesù Rome Italy
European Society for Blood and Marrow Transplantation Pediatric Disease Working Party Paris France
Hematopoietic Stem Cell Transplantation Unit Hematology Oncology Istituto G Gaslini Genova Italy
Instute Portugues Oncologia Lisboa Lisboa Portugal
Pediatric Hematology and Oncology University Hospital Münster Muenster Germany
Pediatric Hematopoietic Transplant Unit Sant Pau Hospital Barcelona Spain
Service of Pediatric Hematology Oncology Hôpital Armand Trousseau Paris France
St Anna Children's Hospital Medical University of Vienna Vienna Austria
Unidad de Hematología y Oncología Pediátrica Hospital Universitario La Paz Madrid Spain
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