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Delayed renal dysfunction after total body irradiation in pediatric malignancies

The purpose of this study was to retrospectively evaluate the incidence of delayed renal dysfunction after total body irradiation (TBI) in long-term survivors of TBI/hematopoietic stem cell transplantation (HSCT). Between 1989 and 2006, 24 pediatric patients underwent TBI as part of the conditioning...

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Autores principales: Watanabe Nemoto, Miho, Isobe, Koichi, Togasaki, Gentaro, Kanazawa, Aki, Kurokawa, Marie, Saito, Makoto, Harada, Rintaro, Kobayashi, Hiroyuki, Ito, Hisao, Uno, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202299/
https://www.ncbi.nlm.nih.gov/pubmed/24914103
http://dx.doi.org/10.1093/jrr/rru041
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author Watanabe Nemoto, Miho
Isobe, Koichi
Togasaki, Gentaro
Kanazawa, Aki
Kurokawa, Marie
Saito, Makoto
Harada, Rintaro
Kobayashi, Hiroyuki
Ito, Hisao
Uno, Takashi
author_facet Watanabe Nemoto, Miho
Isobe, Koichi
Togasaki, Gentaro
Kanazawa, Aki
Kurokawa, Marie
Saito, Makoto
Harada, Rintaro
Kobayashi, Hiroyuki
Ito, Hisao
Uno, Takashi
author_sort Watanabe Nemoto, Miho
collection PubMed
description The purpose of this study was to retrospectively evaluate the incidence of delayed renal dysfunction after total body irradiation (TBI) in long-term survivors of TBI/hematopoietic stem cell transplantation (HSCT). Between 1989 and 2006, 24 pediatric patients underwent TBI as part of the conditioning regimen for HSCT at Chiba University Hospital. Nine patients who survived for more than 5 years were enrolled in this study. No patient had any evidence of renal dysfunction prior to the transplant according to their baseline creatinine levels. The median age at the time of diagnosis was 6 years old (range: 1–17 years old). The follow-up period ranged from 79–170 months (median: 140 months). Renal dysfunction was assessed using the estimated glomerular filtration rate (eGFR). The TBI dose ranged from 8–12 Gy delivered in 3–6 fractions over 2–3 d. The patients were treated with linear accelerators in the supine position, and the radiation was delivered to isocentric right–left and left–right fields via the extended distance technique. The kidneys and the liver were not shielded except in one patient with a left adrenal neuroblastoma. No patient required hemodialysis. The eGFR of four patients (44.4%) progressively decreased. The remaining patients did not demonstrate any eGFR deterioration. Only one patient developed hypertension. By evaluating the changes in eGFR, renal dysfunction among long-term survivors of TBI/HSCT could be detected. Our results suggested that the TBI schedule of 12 Gy in 6 fractions over three consecutive days affects renal function.
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spelling pubmed-42022992014-10-23 Delayed renal dysfunction after total body irradiation in pediatric malignancies Watanabe Nemoto, Miho Isobe, Koichi Togasaki, Gentaro Kanazawa, Aki Kurokawa, Marie Saito, Makoto Harada, Rintaro Kobayashi, Hiroyuki Ito, Hisao Uno, Takashi J Radiat Res Oncology The purpose of this study was to retrospectively evaluate the incidence of delayed renal dysfunction after total body irradiation (TBI) in long-term survivors of TBI/hematopoietic stem cell transplantation (HSCT). Between 1989 and 2006, 24 pediatric patients underwent TBI as part of the conditioning regimen for HSCT at Chiba University Hospital. Nine patients who survived for more than 5 years were enrolled in this study. No patient had any evidence of renal dysfunction prior to the transplant according to their baseline creatinine levels. The median age at the time of diagnosis was 6 years old (range: 1–17 years old). The follow-up period ranged from 79–170 months (median: 140 months). Renal dysfunction was assessed using the estimated glomerular filtration rate (eGFR). The TBI dose ranged from 8–12 Gy delivered in 3–6 fractions over 2–3 d. The patients were treated with linear accelerators in the supine position, and the radiation was delivered to isocentric right–left and left–right fields via the extended distance technique. The kidneys and the liver were not shielded except in one patient with a left adrenal neuroblastoma. No patient required hemodialysis. The eGFR of four patients (44.4%) progressively decreased. The remaining patients did not demonstrate any eGFR deterioration. Only one patient developed hypertension. By evaluating the changes in eGFR, renal dysfunction among long-term survivors of TBI/HSCT could be detected. Our results suggested that the TBI schedule of 12 Gy in 6 fractions over three consecutive days affects renal function. Oxford University Press 2014-09 2014-06-08 /pmc/articles/PMC4202299/ /pubmed/24914103 http://dx.doi.org/10.1093/jrr/rru041 Text en © The Author 2014. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Oncology
Watanabe Nemoto, Miho
Isobe, Koichi
Togasaki, Gentaro
Kanazawa, Aki
Kurokawa, Marie
Saito, Makoto
Harada, Rintaro
Kobayashi, Hiroyuki
Ito, Hisao
Uno, Takashi
Delayed renal dysfunction after total body irradiation in pediatric malignancies
title Delayed renal dysfunction after total body irradiation in pediatric malignancies
title_full Delayed renal dysfunction after total body irradiation in pediatric malignancies
title_fullStr Delayed renal dysfunction after total body irradiation in pediatric malignancies
title_full_unstemmed Delayed renal dysfunction after total body irradiation in pediatric malignancies
title_short Delayed renal dysfunction after total body irradiation in pediatric malignancies
title_sort delayed renal dysfunction after total body irradiation in pediatric malignancies
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202299/
https://www.ncbi.nlm.nih.gov/pubmed/24914103
http://dx.doi.org/10.1093/jrr/rru041
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