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Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas
BACKGROUND: To consolidate literature reports of serious late gastrointestinal toxicities after hypofractionated radiation treatment of pancreatic cancer and attempt to derive normal tissue complication probability (NTCP) parameters using the Lyman-Kutcher-Burman model. METHODS: Published reports of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558934/ https://www.ncbi.nlm.nih.gov/pubmed/26337917 http://dx.doi.org/10.1186/s13014-015-0489-2 |
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author | Elhammali, Adnan Patel, Mukund Weinberg, Benjamin Verma, Vivek Liu, Jingxia Olsen, Jeffrey R. Gay, Hiram A. |
author_facet | Elhammali, Adnan Patel, Mukund Weinberg, Benjamin Verma, Vivek Liu, Jingxia Olsen, Jeffrey R. Gay, Hiram A. |
author_sort | Elhammali, Adnan |
collection | PubMed |
description | BACKGROUND: To consolidate literature reports of serious late gastrointestinal toxicities after hypofractionated radiation treatment of pancreatic cancer and attempt to derive normal tissue complication probability (NTCP) parameters using the Lyman-Kutcher-Burman model. METHODS: Published reports of late grade 3 or greater gastrointestinal toxicity after hypofractionated treatment of pancreatic cancer were reviewed. The biologically equivalent dose in 1.8 Gy fractions was calculated using the EQD model. NTCP parameters were calculated using the LKB model assuming 1–5 % of the normal tissue volume was exposed to the prescription dose with α/β ratios of 3 or 4. RESULTS: A total of 16 human studies were examined encompassing a total of 1160 patients. Toxicities consisted of ulcers, hemorrhages, obstructions, strictures, and perforations. Non-hemorrhagic and non-perforated ulcers occurred at a rate of 9.1 % and were the most commonly reported toxicity. Derived NTCP parameter ranges were as follows: n = 0.38–0.63, m = 0.48–0.49, and TD(50) = 35–95 Gy. Regression analysis showed that among various study characteristics, dose was the only significant predictor of toxicity. CONCLUSIONS: Published gastrointestinal toxicity reports after hypofractionated radiotherapy for pancreatic cancer were compiled. Median dose was predictive of late grade ≥ 3 gastrointestinal toxicity. Preliminary NTCP parameters were derived for multiple volume constraints. |
format | Online Article Text |
id | pubmed-4558934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45589342015-09-04 Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas Elhammali, Adnan Patel, Mukund Weinberg, Benjamin Verma, Vivek Liu, Jingxia Olsen, Jeffrey R. Gay, Hiram A. Radiat Oncol Research BACKGROUND: To consolidate literature reports of serious late gastrointestinal toxicities after hypofractionated radiation treatment of pancreatic cancer and attempt to derive normal tissue complication probability (NTCP) parameters using the Lyman-Kutcher-Burman model. METHODS: Published reports of late grade 3 or greater gastrointestinal toxicity after hypofractionated treatment of pancreatic cancer were reviewed. The biologically equivalent dose in 1.8 Gy fractions was calculated using the EQD model. NTCP parameters were calculated using the LKB model assuming 1–5 % of the normal tissue volume was exposed to the prescription dose with α/β ratios of 3 or 4. RESULTS: A total of 16 human studies were examined encompassing a total of 1160 patients. Toxicities consisted of ulcers, hemorrhages, obstructions, strictures, and perforations. Non-hemorrhagic and non-perforated ulcers occurred at a rate of 9.1 % and were the most commonly reported toxicity. Derived NTCP parameter ranges were as follows: n = 0.38–0.63, m = 0.48–0.49, and TD(50) = 35–95 Gy. Regression analysis showed that among various study characteristics, dose was the only significant predictor of toxicity. CONCLUSIONS: Published gastrointestinal toxicity reports after hypofractionated radiotherapy for pancreatic cancer were compiled. Median dose was predictive of late grade ≥ 3 gastrointestinal toxicity. Preliminary NTCP parameters were derived for multiple volume constraints. BioMed Central 2015-09-04 /pmc/articles/PMC4558934/ /pubmed/26337917 http://dx.doi.org/10.1186/s13014-015-0489-2 Text en © Elhammali et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Elhammali, Adnan Patel, Mukund Weinberg, Benjamin Verma, Vivek Liu, Jingxia Olsen, Jeffrey R. Gay, Hiram A. Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas |
title | Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas |
title_full | Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas |
title_fullStr | Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas |
title_full_unstemmed | Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas |
title_short | Late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas |
title_sort | late gastrointestinal tissue effects after hypofractionated radiation therapy of the pancreas |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558934/ https://www.ncbi.nlm.nih.gov/pubmed/26337917 http://dx.doi.org/10.1186/s13014-015-0489-2 |
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