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To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL

Thyroid disorders are well-studied after allogeneic haematopoietic stem cell transplantation (HSCT) following total body irradiation (TBI)-based conditioning, occurring in 15–30% of paediatric survivors. The toxic effect of TBI is known but data on the role of immunological dysregulation (ID) and ch...

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Autores principales: Zubarovskaya, Natalia, Bauer, Dorothea, Ronceray, Leila, Poetschger, Ulrike, Kurzmann, Paulina, Lender, Carina, Kuzmina, Zoya, Lawitschka, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809136/
https://www.ncbi.nlm.nih.gov/pubmed/35127596
http://dx.doi.org/10.3389/fped.2021.798974
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author Zubarovskaya, Natalia
Bauer, Dorothea
Ronceray, Leila
Poetschger, Ulrike
Kurzmann, Paulina
Lender, Carina
Kuzmina, Zoya
Lawitschka, Anita
author_facet Zubarovskaya, Natalia
Bauer, Dorothea
Ronceray, Leila
Poetschger, Ulrike
Kurzmann, Paulina
Lender, Carina
Kuzmina, Zoya
Lawitschka, Anita
author_sort Zubarovskaya, Natalia
collection PubMed
description Thyroid disorders are well-studied after allogeneic haematopoietic stem cell transplantation (HSCT) following total body irradiation (TBI)-based conditioning, occurring in 15–30% of paediatric survivors. The toxic effect of TBI is known but data on the role of immunological dysregulation (ID) and chronic graft-versus-host-disease (cGvHD) are scarce. We studied functional and structural thyroid disorders in 97 paediatric ALL patients after TBI-based HSCT, assessing their correlation with patient/transplant characteristics including cGvHD, prolonged immunosuppression and ID. The 10- and 15-year cumulative incidence (CI) of functional disorders was 50 and 60%. Univariate analysis revealed TBI in 6 vs. 8 fractions (p = 0.01), an interval between ALL diagnosis and HSCT <1 year (p = 0.038), and the application of ATG (p = 0.044) as risk factors. The 10- and 15-year CI of structural disorders was 60 and 80%. No correlation between patient/transplant characteristics and structural disorders was observed. cGvHD, prolonged immunosuppression and additional radiotherapy were not associated with any thyroid disease. We observed a significant correlation between ID and the development of thyroid dysfunction in patients with structural changes (10-year CI: 77% for patients with ID vs. 56% without ID, p = 0.02). The impact of our results on thyroid follow-up evaluations and the significance of hormonal replacement therapy are discussed.
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spelling pubmed-88091362022-02-03 To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL Zubarovskaya, Natalia Bauer, Dorothea Ronceray, Leila Poetschger, Ulrike Kurzmann, Paulina Lender, Carina Kuzmina, Zoya Lawitschka, Anita Front Pediatr Pediatrics Thyroid disorders are well-studied after allogeneic haematopoietic stem cell transplantation (HSCT) following total body irradiation (TBI)-based conditioning, occurring in 15–30% of paediatric survivors. The toxic effect of TBI is known but data on the role of immunological dysregulation (ID) and chronic graft-versus-host-disease (cGvHD) are scarce. We studied functional and structural thyroid disorders in 97 paediatric ALL patients after TBI-based HSCT, assessing their correlation with patient/transplant characteristics including cGvHD, prolonged immunosuppression and ID. The 10- and 15-year cumulative incidence (CI) of functional disorders was 50 and 60%. Univariate analysis revealed TBI in 6 vs. 8 fractions (p = 0.01), an interval between ALL diagnosis and HSCT <1 year (p = 0.038), and the application of ATG (p = 0.044) as risk factors. The 10- and 15-year CI of structural disorders was 60 and 80%. No correlation between patient/transplant characteristics and structural disorders was observed. cGvHD, prolonged immunosuppression and additional radiotherapy were not associated with any thyroid disease. We observed a significant correlation between ID and the development of thyroid dysfunction in patients with structural changes (10-year CI: 77% for patients with ID vs. 56% without ID, p = 0.02). The impact of our results on thyroid follow-up evaluations and the significance of hormonal replacement therapy are discussed. Frontiers Media S.A. 2022-01-19 /pmc/articles/PMC8809136/ /pubmed/35127596 http://dx.doi.org/10.3389/fped.2021.798974 Text en Copyright © 2022 Zubarovskaya, Bauer, Ronceray, Poetschger, Kurzmann, Lender, Kuzmina and Lawitschka. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Zubarovskaya, Natalia
Bauer, Dorothea
Ronceray, Leila
Poetschger, Ulrike
Kurzmann, Paulina
Lender, Carina
Kuzmina, Zoya
Lawitschka, Anita
To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL
title To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL
title_full To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL
title_fullStr To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL
title_full_unstemmed To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL
title_short To Lighten the Burden of Cure: Thyroid Disease in Long-Term Survivors After TBI Conditioning for Paediatric ALL
title_sort to lighten the burden of cure: thyroid disease in long-term survivors after tbi conditioning for paediatric all
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809136/
https://www.ncbi.nlm.nih.gov/pubmed/35127596
http://dx.doi.org/10.3389/fped.2021.798974
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