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The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy

PURPOSE: To compare treatment plans for interstitial high dose rate (HDR) liver brachytherapy with (192)Ir calculated according to current-standard TG-43U1 protocol with model-based dose calculation following TG-186 protocol. METHODS: We retrospectively evaluated dose volume histogram (DVH) paramete...

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Autores principales: Duque, Anna Sophie, Corradini, Stefanie, Kamp, Florian, Seidensticker, Max, Streitparth, Florian, Kurz, Christopher, Walter, Franziska, Parodi, Katia, Verhaegen, Frank, Ricke, Jens, Belka, Claus, Fonseca, Gabriel Paiva, Landry, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063719/
https://www.ncbi.nlm.nih.gov/pubmed/32151255
http://dx.doi.org/10.1186/s13014-020-01492-9
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author Duque, Anna Sophie
Corradini, Stefanie
Kamp, Florian
Seidensticker, Max
Streitparth, Florian
Kurz, Christopher
Walter, Franziska
Parodi, Katia
Verhaegen, Frank
Ricke, Jens
Belka, Claus
Fonseca, Gabriel Paiva
Landry, Guillaume
author_facet Duque, Anna Sophie
Corradini, Stefanie
Kamp, Florian
Seidensticker, Max
Streitparth, Florian
Kurz, Christopher
Walter, Franziska
Parodi, Katia
Verhaegen, Frank
Ricke, Jens
Belka, Claus
Fonseca, Gabriel Paiva
Landry, Guillaume
author_sort Duque, Anna Sophie
collection PubMed
description PURPOSE: To compare treatment plans for interstitial high dose rate (HDR) liver brachytherapy with (192)Ir calculated according to current-standard TG-43U1 protocol with model-based dose calculation following TG-186 protocol. METHODS: We retrospectively evaluated dose volume histogram (DVH) parameters for liver, organs at risk (OARs) and clinical target volumes (CTVs) of 20 patient cases diagnosed with hepatocellular carcinoma (HCC) or metastatic colorectal cancer (mCRC). Dose calculations on a homogeneous water geometry (TG-43U1 surrogate) and on a computed tomography (CT) based geometry (TG-186) were performed using Monte Carlo (MC) simulations. The CTs were segmented based on a combination of assigning TG-186 recommended tissues to fixed Hounsfield Unit (HU) ranges and using organ contours delineated by physicians. For the liver, V(5Gy) and V(10Gy) were analysed, and for OARs the dose to 1 cubic centimeter (D(1cc)). Target coverage was assessed by calculating V(150), V(100), V(95) and V(90) as well as D(95) and D(90). For every DVH parameter, median, minimum and maximum values of the deviations of TG-186 from TG-43U1 were analysed. RESULTS: TG-186-calculated dose was found to be on average lower than dose calculated with TG-43U1. The deviation of highest magnitude for liver parameters was -6.2% of the total liver volume. For OARs, the deviations were all smaller than or equal to -0.5 Gy. Target coverage deviations were as high as -1.5% of the total CTV volume and -3.5% of the prescribed dose. CONCLUSIONS: In this study we found that TG-43U1 overestimates dose to liver tissue compared to TG-186. This finding may be of clinical importance for cases where dose to the whole liver is the limiting factor.
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spelling pubmed-70637192020-03-13 The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy Duque, Anna Sophie Corradini, Stefanie Kamp, Florian Seidensticker, Max Streitparth, Florian Kurz, Christopher Walter, Franziska Parodi, Katia Verhaegen, Frank Ricke, Jens Belka, Claus Fonseca, Gabriel Paiva Landry, Guillaume Radiat Oncol Research PURPOSE: To compare treatment plans for interstitial high dose rate (HDR) liver brachytherapy with (192)Ir calculated according to current-standard TG-43U1 protocol with model-based dose calculation following TG-186 protocol. METHODS: We retrospectively evaluated dose volume histogram (DVH) parameters for liver, organs at risk (OARs) and clinical target volumes (CTVs) of 20 patient cases diagnosed with hepatocellular carcinoma (HCC) or metastatic colorectal cancer (mCRC). Dose calculations on a homogeneous water geometry (TG-43U1 surrogate) and on a computed tomography (CT) based geometry (TG-186) were performed using Monte Carlo (MC) simulations. The CTs were segmented based on a combination of assigning TG-186 recommended tissues to fixed Hounsfield Unit (HU) ranges and using organ contours delineated by physicians. For the liver, V(5Gy) and V(10Gy) were analysed, and for OARs the dose to 1 cubic centimeter (D(1cc)). Target coverage was assessed by calculating V(150), V(100), V(95) and V(90) as well as D(95) and D(90). For every DVH parameter, median, minimum and maximum values of the deviations of TG-186 from TG-43U1 were analysed. RESULTS: TG-186-calculated dose was found to be on average lower than dose calculated with TG-43U1. The deviation of highest magnitude for liver parameters was -6.2% of the total liver volume. For OARs, the deviations were all smaller than or equal to -0.5 Gy. Target coverage deviations were as high as -1.5% of the total CTV volume and -3.5% of the prescribed dose. CONCLUSIONS: In this study we found that TG-43U1 overestimates dose to liver tissue compared to TG-186. This finding may be of clinical importance for cases where dose to the whole liver is the limiting factor. BioMed Central 2020-03-09 /pmc/articles/PMC7063719/ /pubmed/32151255 http://dx.doi.org/10.1186/s13014-020-01492-9 Text en © The Author(s) 2020 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
Duque, Anna Sophie
Corradini, Stefanie
Kamp, Florian
Seidensticker, Max
Streitparth, Florian
Kurz, Christopher
Walter, Franziska
Parodi, Katia
Verhaegen, Frank
Ricke, Jens
Belka, Claus
Fonseca, Gabriel Paiva
Landry, Guillaume
The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy
title The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy
title_full The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy
title_fullStr The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy
title_full_unstemmed The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy
title_short The dosimetric impact of replacing the TG-43 algorithm by model based dose calculation for liver brachytherapy
title_sort dosimetric impact of replacing the tg-43 algorithm by model based dose calculation for liver brachytherapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063719/
https://www.ncbi.nlm.nih.gov/pubmed/32151255
http://dx.doi.org/10.1186/s13014-020-01492-9
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