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Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation

Treatment-related mortality and morbidity remain a challenge in hematopoietic stem cell transplantation (HSCT). In this retrospective, single-center study, we analyzed endothelial damage as a potential, common denominator and mechanism for the adverse effects. We evaluated the prevalence of key vasc...

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Autores principales: Leimi, Lilli, Jahnukainen, Kirsi, Olkinuora, Helena, Meri, Seppo, Vettenranta, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090633/
https://www.ncbi.nlm.nih.gov/pubmed/35177827
http://dx.doi.org/10.1038/s41409-022-01607-8
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author Leimi, Lilli
Jahnukainen, Kirsi
Olkinuora, Helena
Meri, Seppo
Vettenranta, Kim
author_facet Leimi, Lilli
Jahnukainen, Kirsi
Olkinuora, Helena
Meri, Seppo
Vettenranta, Kim
author_sort Leimi, Lilli
collection PubMed
description Treatment-related mortality and morbidity remain a challenge in hematopoietic stem cell transplantation (HSCT). In this retrospective, single-center study, we analyzed endothelial damage as a potential, common denominator and mechanism for the adverse effects. We evaluated the prevalence of key vascular complications and graft-versus-host disease among 122 pediatric patients with an allogeneic HSCT between 2001 and 2013. The spectrum and frequency of acute adverse events emerging ≤100 days post transplant were graded according to the CTCAE 4.03 and analyzed. We identified a total of 19/122 (15.6%) patients with vascular complications, fulfilling the criteria of capillary leak syndrome, veno-occlusive disease/sinusoidal obstruction syndrome or thrombotic microangiopathy. The patients had a poorer overall survival (77% versus 26%, p < 0.001). Nearly one half (56/122, 45.9%) had at least one, severe (grade 3 or 4) adverse event. Patients with vascular complications had more often edema/effusions (p = 0.023), thrombocytopenia (p = 0.001), gastrointestinal bleeding (p < 0.001), acute kidney injury (p < 0.001), ascites (p < 0.001) or bilirubin increase (p = 0.027). These endotheliopathy-related adverse events appeared early post HSCT, varied in their clinical phenotype and predicted a poor outcome. An unrelated donor but not previous exposure to leukemia or irradiation-based conditioning was identified as a risk factor for vascular complications and endotheliopathy.
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spelling pubmed-90906332022-05-12 Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation Leimi, Lilli Jahnukainen, Kirsi Olkinuora, Helena Meri, Seppo Vettenranta, Kim Bone Marrow Transplant Article Treatment-related mortality and morbidity remain a challenge in hematopoietic stem cell transplantation (HSCT). In this retrospective, single-center study, we analyzed endothelial damage as a potential, common denominator and mechanism for the adverse effects. We evaluated the prevalence of key vascular complications and graft-versus-host disease among 122 pediatric patients with an allogeneic HSCT between 2001 and 2013. The spectrum and frequency of acute adverse events emerging ≤100 days post transplant were graded according to the CTCAE 4.03 and analyzed. We identified a total of 19/122 (15.6%) patients with vascular complications, fulfilling the criteria of capillary leak syndrome, veno-occlusive disease/sinusoidal obstruction syndrome or thrombotic microangiopathy. The patients had a poorer overall survival (77% versus 26%, p < 0.001). Nearly one half (56/122, 45.9%) had at least one, severe (grade 3 or 4) adverse event. Patients with vascular complications had more often edema/effusions (p = 0.023), thrombocytopenia (p = 0.001), gastrointestinal bleeding (p < 0.001), acute kidney injury (p < 0.001), ascites (p < 0.001) or bilirubin increase (p = 0.027). These endotheliopathy-related adverse events appeared early post HSCT, varied in their clinical phenotype and predicted a poor outcome. An unrelated donor but not previous exposure to leukemia or irradiation-based conditioning was identified as a risk factor for vascular complications and endotheliopathy. Nature Publishing Group UK 2022-02-17 2022 /pmc/articles/PMC9090633/ /pubmed/35177827 http://dx.doi.org/10.1038/s41409-022-01607-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Leimi, Lilli
Jahnukainen, Kirsi
Olkinuora, Helena
Meri, Seppo
Vettenranta, Kim
Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
title Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
title_full Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
title_fullStr Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
title_full_unstemmed Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
title_short Early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
title_sort early vascular toxicity after pediatric allogeneic hematopoietic stem cell transplantation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090633/
https://www.ncbi.nlm.nih.gov/pubmed/35177827
http://dx.doi.org/10.1038/s41409-022-01607-8
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