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Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes
Despite the well‐known benefits of positron emission tomography (PET) imaging in lung cancer diagnosis and staging, the poor spatial resolution of PET has limited its use in radiotherapy planning. Methods used for segmenting tumor from normal tissue, such as threshold boundaries using a fraction of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723457/ https://www.ncbi.nlm.nih.gov/pubmed/16421501 http://dx.doi.org/10.1120/jacmp.v6i4.2156 |
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author | Chetty, Indrin J. Fernando, Shaneli Kessler, Marc L. Mcshan, Daniel L. Brooks, Cassandra Ten Haken, Randall K. (Spring) Kong, Feng‐Ming |
author_facet | Chetty, Indrin J. Fernando, Shaneli Kessler, Marc L. Mcshan, Daniel L. Brooks, Cassandra Ten Haken, Randall K. (Spring) Kong, Feng‐Ming |
author_sort | Chetty, Indrin J. |
collection | PubMed |
description | Despite the well‐known benefits of positron emission tomography (PET) imaging in lung cancer diagnosis and staging, the poor spatial resolution of PET has limited its use in radiotherapy planning. Methods used for segmenting tumor from normal tissue, such as threshold boundaries using a fraction of the standardized uptake value (SUV), are subject to uncertainties. The issue of respiratory motion in the thorax confounds the problem of accurate target definition. In this work, we evaluate how changing the PET‐defined target volume by varying the threshold value in the segmentation process impacts target and normal lung tissue doses. For each of eight lung cancer patients we retrospectively generated multiple PET‐target volumes; each target volume corresponds to those voxels with intensities above a given threshold level, defined by a percentage of the maximum voxel intensity. PET‐defined targets were compared to those from CT; CT targets comprise a composite volume generated from breath‐hold inhale and exhale datasets; the CT dataset therefore also includes the extents of tumor motion. Treatment plans using Monte Carlo dose calculation were generated for all targets; the dose uniformity was approximately [Formula: see text] within the internal target volume (ITV) (formed by a uniform 8‐mm expansion of the composite gross target volume (GTV)). In all cases differences were observed in the generalized equivalent uniform doses (gEUDs) to the targets and in the mean lung doses (MLDs) and normal tissue complication probabilities (NTCPs) to the normal lung tissues. The magnitudes of the dose differences were found to depend on the target volume, location, and amount of irradiated normal lung tissue, and in many instances were clinically meaningful (greater than a single 2 Gy fraction). For those patients studied, results indicate that accurate dosimetry using PET volumes is highly dependent on accurate target segmentation. Further study with correlation to clinical outcome will be helpful in determining how to apply these various PET and CT volumes in treatment planning, to potentially improve local tumor control and reduce normal tissue toxicities. PACS number: 87.52.Tf |
format | Online Article Text |
id | pubmed-5723457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57234572018-04-02 Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes Chetty, Indrin J. Fernando, Shaneli Kessler, Marc L. Mcshan, Daniel L. Brooks, Cassandra Ten Haken, Randall K. (Spring) Kong, Feng‐Ming J Appl Clin Med Phys Radiation Oncology Physics Despite the well‐known benefits of positron emission tomography (PET) imaging in lung cancer diagnosis and staging, the poor spatial resolution of PET has limited its use in radiotherapy planning. Methods used for segmenting tumor from normal tissue, such as threshold boundaries using a fraction of the standardized uptake value (SUV), are subject to uncertainties. The issue of respiratory motion in the thorax confounds the problem of accurate target definition. In this work, we evaluate how changing the PET‐defined target volume by varying the threshold value in the segmentation process impacts target and normal lung tissue doses. For each of eight lung cancer patients we retrospectively generated multiple PET‐target volumes; each target volume corresponds to those voxels with intensities above a given threshold level, defined by a percentage of the maximum voxel intensity. PET‐defined targets were compared to those from CT; CT targets comprise a composite volume generated from breath‐hold inhale and exhale datasets; the CT dataset therefore also includes the extents of tumor motion. Treatment plans using Monte Carlo dose calculation were generated for all targets; the dose uniformity was approximately [Formula: see text] within the internal target volume (ITV) (formed by a uniform 8‐mm expansion of the composite gross target volume (GTV)). In all cases differences were observed in the generalized equivalent uniform doses (gEUDs) to the targets and in the mean lung doses (MLDs) and normal tissue complication probabilities (NTCPs) to the normal lung tissues. The magnitudes of the dose differences were found to depend on the target volume, location, and amount of irradiated normal lung tissue, and in many instances were clinically meaningful (greater than a single 2 Gy fraction). For those patients studied, results indicate that accurate dosimetry using PET volumes is highly dependent on accurate target segmentation. Further study with correlation to clinical outcome will be helpful in determining how to apply these various PET and CT volumes in treatment planning, to potentially improve local tumor control and reduce normal tissue toxicities. PACS number: 87.52.Tf John Wiley and Sons Inc. 2005-11-22 /pmc/articles/PMC5723457/ /pubmed/16421501 http://dx.doi.org/10.1120/jacmp.v6i4.2156 Text en © 2005 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 | Radiation Oncology Physics Chetty, Indrin J. Fernando, Shaneli Kessler, Marc L. Mcshan, Daniel L. Brooks, Cassandra Ten Haken, Randall K. (Spring) Kong, Feng‐Ming Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes |
title | Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes |
title_full | Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes |
title_fullStr | Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes |
title_full_unstemmed | Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes |
title_short | Monte Carlo‐based lung cancer treatment planning incorporating PET‐defined target volumes |
title_sort | monte carlo‐based lung cancer treatment planning incorporating pet‐defined target volumes |
topic | Radiation Oncology Physics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723457/ https://www.ncbi.nlm.nih.gov/pubmed/16421501 http://dx.doi.org/10.1120/jacmp.v6i4.2156 |
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