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Depth dose perturbation by a hydrogel fiducial marker in a proton beam

The purpose of this study was to evaluate proton depth dose perturbation caused by a radio‐opaque hydrogel fiducial marker. Electronic proton stopping powers in the hydrogel were calculated for energies 0.5–250 MeV, and Monte Carlo simulations were generated of hydrogel vs. gold markers placed at va...

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Detalles Bibliográficos
Autores principales: Zhang, Miao, Reyhan, Meral, Kim, Leonard H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689967/
https://www.ncbi.nlm.nih.gov/pubmed/25679167
http://dx.doi.org/10.1120/jacmp.v16i1.5090
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author Zhang, Miao
Reyhan, Meral
Kim, Leonard H.
author_facet Zhang, Miao
Reyhan, Meral
Kim, Leonard H.
author_sort Zhang, Miao
collection PubMed
description The purpose of this study was to evaluate proton depth dose perturbation caused by a radio‐opaque hydrogel fiducial marker. Electronic proton stopping powers in the hydrogel were calculated for energies 0.5–250 MeV, and Monte Carlo simulations were generated of hydrogel vs. gold markers placed at various water phantom depths in a generic proton beam. Across the studied energy range, the gel/water stopping power ratio was 1.0146 to 1.0160. In the Monte Carlo simulation, the hydrogel marker caused no discernible perturbation of the proton percent depth‐dose (PDD) curve. In contrast, the gold marker caused dose reductions of as much as 20% and dose shadowing regions as long as 6.5 cm. In contrast to gold markers, the radio‐opaque hydrogel marker causes negligible proton depth dose perturbation. This factor may be taken into consideration for image‐guided proton therapy at facilities with suitable imaging modalities. PACS number: 87.55.Qr
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spelling pubmed-56899672018-04-02 Depth dose perturbation by a hydrogel fiducial marker in a proton beam Zhang, Miao Reyhan, Meral Kim, Leonard H. J Appl Clin Med Phys Technical Notes The purpose of this study was to evaluate proton depth dose perturbation caused by a radio‐opaque hydrogel fiducial marker. Electronic proton stopping powers in the hydrogel were calculated for energies 0.5–250 MeV, and Monte Carlo simulations were generated of hydrogel vs. gold markers placed at various water phantom depths in a generic proton beam. Across the studied energy range, the gel/water stopping power ratio was 1.0146 to 1.0160. In the Monte Carlo simulation, the hydrogel marker caused no discernible perturbation of the proton percent depth‐dose (PDD) curve. In contrast, the gold marker caused dose reductions of as much as 20% and dose shadowing regions as long as 6.5 cm. In contrast to gold markers, the radio‐opaque hydrogel marker causes negligible proton depth dose perturbation. This factor may be taken into consideration for image‐guided proton therapy at facilities with suitable imaging modalities. PACS number: 87.55.Qr John Wiley and Sons Inc. 2015-01-08 /pmc/articles/PMC5689967/ /pubmed/25679167 http://dx.doi.org/10.1120/jacmp.v16i1.5090 Text en © 2015 The Authors. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Notes
Zhang, Miao
Reyhan, Meral
Kim, Leonard H.
Depth dose perturbation by a hydrogel fiducial marker in a proton beam
title Depth dose perturbation by a hydrogel fiducial marker in a proton beam
title_full Depth dose perturbation by a hydrogel fiducial marker in a proton beam
title_fullStr Depth dose perturbation by a hydrogel fiducial marker in a proton beam
title_full_unstemmed Depth dose perturbation by a hydrogel fiducial marker in a proton beam
title_short Depth dose perturbation by a hydrogel fiducial marker in a proton beam
title_sort depth dose perturbation by a hydrogel fiducial marker in a proton beam
topic Technical Notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689967/
https://www.ncbi.nlm.nih.gov/pubmed/25679167
http://dx.doi.org/10.1120/jacmp.v16i1.5090
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