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The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model

This study was undertaken to assess the diagnostic value of 2-[(18)F]-fluoro-2-deoxy-D-glucose positron emission tomography with computed tomography ([(18)F]-FDG-PET/CT) in the detection of radiation toxicity in normal bone marrow using Tibet minipigs as a model. Eighteen Tibet minipigs were caged i...

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Detalles Bibliográficos
Autores principales: Chen, Chi, Yan, Li-Meng, Guo, Kun-Yuan, Wang, Yu-Jue, Zou, Fei, Gu, Wei-Wang, Tang, Hua, Li, Yan-Ling, Wu, Shao-Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393352/
https://www.ncbi.nlm.nih.gov/pubmed/22843618
http://dx.doi.org/10.1093/jrr/rrs006
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author Chen, Chi
Yan, Li-Meng
Guo, Kun-Yuan
Wang, Yu-Jue
Zou, Fei
Gu, Wei-Wang
Tang, Hua
Li, Yan-Ling
Wu, Shao-Jie
author_facet Chen, Chi
Yan, Li-Meng
Guo, Kun-Yuan
Wang, Yu-Jue
Zou, Fei
Gu, Wei-Wang
Tang, Hua
Li, Yan-Ling
Wu, Shao-Jie
author_sort Chen, Chi
collection PubMed
description This study was undertaken to assess the diagnostic value of 2-[(18)F]-fluoro-2-deoxy-D-glucose positron emission tomography with computed tomography ([(18)F]-FDG-PET/CT) in the detection of radiation toxicity in normal bone marrow using Tibet minipigs as a model. Eighteen Tibet minipigs were caged in aseptic rooms and randomly divided into six groups. Five groups (n = 3/group) were irradiated with single doses of 2, 5, 8, 11 and 14 Gy of total body irradiation (TBI) using an 8-MV X-ray linear accelerator. These pigs were evaluated with [(18)F]-FDG-PET/CT, and their marrow nucleated cells were counted. The data were initially collected at 6, 24 and 72 h after treatment and were then collected on Days 5–60 post-TBI at 5-day intervals. At 24 and 72 h post-TBI, marrow standardized uptake value (SUV) data showed a dose-dependent decrease in the radiation dose range from 2–8 Gy. Upon long-term observation, SUV and marrow nucleated cell number in the 11-Gy and 14-Gy groups showed a continuous and marked reduction throughout the entire time course, while Kaplan–Meier curves of survival showed low survival. In contrast, the SUVs in the 2-, 5- and 8-Gy groups showed early transient increases followed by a decline from approximately 72 h through Days 5–15 and then normalized or maintained low levels through the endpoint; marrow nucleated cell number and survival curves showed approximately the same trend and higher survival, respectively. Our findings suggest that [(18)F]-FDG-PET/CT may be helpful in quickly assessing the absorbed doses and predicting the prognosis in patients.
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spelling pubmed-33933522013-07-01 The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model Chen, Chi Yan, Li-Meng Guo, Kun-Yuan Wang, Yu-Jue Zou, Fei Gu, Wei-Wang Tang, Hua Li, Yan-Ling Wu, Shao-Jie J Radiat Res Biology This study was undertaken to assess the diagnostic value of 2-[(18)F]-fluoro-2-deoxy-D-glucose positron emission tomography with computed tomography ([(18)F]-FDG-PET/CT) in the detection of radiation toxicity in normal bone marrow using Tibet minipigs as a model. Eighteen Tibet minipigs were caged in aseptic rooms and randomly divided into six groups. Five groups (n = 3/group) were irradiated with single doses of 2, 5, 8, 11 and 14 Gy of total body irradiation (TBI) using an 8-MV X-ray linear accelerator. These pigs were evaluated with [(18)F]-FDG-PET/CT, and their marrow nucleated cells were counted. The data were initially collected at 6, 24 and 72 h after treatment and were then collected on Days 5–60 post-TBI at 5-day intervals. At 24 and 72 h post-TBI, marrow standardized uptake value (SUV) data showed a dose-dependent decrease in the radiation dose range from 2–8 Gy. Upon long-term observation, SUV and marrow nucleated cell number in the 11-Gy and 14-Gy groups showed a continuous and marked reduction throughout the entire time course, while Kaplan–Meier curves of survival showed low survival. In contrast, the SUVs in the 2-, 5- and 8-Gy groups showed early transient increases followed by a decline from approximately 72 h through Days 5–15 and then normalized or maintained low levels through the endpoint; marrow nucleated cell number and survival curves showed approximately the same trend and higher survival, respectively. Our findings suggest that [(18)F]-FDG-PET/CT may be helpful in quickly assessing the absorbed doses and predicting the prognosis in patients. Oxford University Press 2012-07 2012-06-06 /pmc/articles/PMC3393352/ /pubmed/22843618 http://dx.doi.org/10.1093/jrr/rrs006 Text en © The Author 2012. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology. http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Biology
Chen, Chi
Yan, Li-Meng
Guo, Kun-Yuan
Wang, Yu-Jue
Zou, Fei
Gu, Wei-Wang
Tang, Hua
Li, Yan-Ling
Wu, Shao-Jie
The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model
title The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model
title_full The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model
title_fullStr The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model
title_full_unstemmed The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model
title_short The diagnostic value of [(18)F]-FDG-PET/CT in hematopoietic radiation toxicity: a Tibet minipig model
title_sort diagnostic value of [(18)f]-fdg-pet/ct in hematopoietic radiation toxicity: a tibet minipig model
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393352/
https://www.ncbi.nlm.nih.gov/pubmed/22843618
http://dx.doi.org/10.1093/jrr/rrs006
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