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Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors

Substantial disagreement exists over appropriate PET segmentation techniques for non‐small cell lung cancer. Currently, no segmentation algorithm explicitly considers tumor motion in determining tumor borders. We developed an automatic PET segmentation model as a function of target volume, motion ex...

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Autores principales: Riegel, Adam C., Bucci, M. Kara, Mawlawi, Osama R., Ahmad, Moiz, Luo, Dershan, Chandler, Adam, Pan, Tinsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711243/
https://www.ncbi.nlm.nih.gov/pubmed/24423860
http://dx.doi.org/10.1120/jacmp.v15i1.4600
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author Riegel, Adam C.
Bucci, M. Kara
Mawlawi, Osama R.
Ahmad, Moiz
Luo, Dershan
Chandler, Adam
Pan, Tinsu
author_facet Riegel, Adam C.
Bucci, M. Kara
Mawlawi, Osama R.
Ahmad, Moiz
Luo, Dershan
Chandler, Adam
Pan, Tinsu
author_sort Riegel, Adam C.
collection PubMed
description Substantial disagreement exists over appropriate PET segmentation techniques for non‐small cell lung cancer. Currently, no segmentation algorithm explicitly considers tumor motion in determining tumor borders. We developed an automatic PET segmentation model as a function of target volume, motion extent, and source‐to‐background ratio (the VMSBR model). The purpose of this work was to apply the VMSBR model and six other segmentation algorithms to a sample of lung tumors. PET and 4D CT were performed in the same imaging session for 23 patients (24 tumors) for radiation therapy planning. Internal target volumes (ITVs) were autosegmented on maximum intensity projection (MIP) of cine CT. ITVs were delineated on PET using the following methods: 15%, 35%, and 42% of maximum activity concentration, standardized uptake value (SUV) of 2.5 g/mL, 15% of mean activity concentration plus background, a linear function of mean SUV, and the VMSBR model. Predicted threshold values from each method were compared to measured optimal threshold values, and resulting volume magnitudes were compared to cine‐CT‐derived ITV Correlation between predicted and measured threshold values ranged from slopes of 0.29 for the simplest single‐threshold techniques to 0.90 for the VMSBR technique. [Formula: see text] values ranged from 0.07 for the simplest single‐threshold techniques to 0.86 for the VMSBR technique. The VMSBR segmentation technique that included volume, motion, and source‐to‐background ratio, produced accurate ITVs in patients when compared with cine‐CT‐derived ITV. PACS number: 87.57.nm
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spelling pubmed-57112432018-04-02 Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors Riegel, Adam C. Bucci, M. Kara Mawlawi, Osama R. Ahmad, Moiz Luo, Dershan Chandler, Adam Pan, Tinsu J Appl Clin Med Phys Radiation Oncology Physics Substantial disagreement exists over appropriate PET segmentation techniques for non‐small cell lung cancer. Currently, no segmentation algorithm explicitly considers tumor motion in determining tumor borders. We developed an automatic PET segmentation model as a function of target volume, motion extent, and source‐to‐background ratio (the VMSBR model). The purpose of this work was to apply the VMSBR model and six other segmentation algorithms to a sample of lung tumors. PET and 4D CT were performed in the same imaging session for 23 patients (24 tumors) for radiation therapy planning. Internal target volumes (ITVs) were autosegmented on maximum intensity projection (MIP) of cine CT. ITVs were delineated on PET using the following methods: 15%, 35%, and 42% of maximum activity concentration, standardized uptake value (SUV) of 2.5 g/mL, 15% of mean activity concentration plus background, a linear function of mean SUV, and the VMSBR model. Predicted threshold values from each method were compared to measured optimal threshold values, and resulting volume magnitudes were compared to cine‐CT‐derived ITV Correlation between predicted and measured threshold values ranged from slopes of 0.29 for the simplest single‐threshold techniques to 0.90 for the VMSBR technique. [Formula: see text] values ranged from 0.07 for the simplest single‐threshold techniques to 0.86 for the VMSBR technique. The VMSBR segmentation technique that included volume, motion, and source‐to‐background ratio, produced accurate ITVs in patients when compared with cine‐CT‐derived ITV. PACS number: 87.57.nm John Wiley and Sons Inc. 2014-01-06 /pmc/articles/PMC5711243/ /pubmed/24423860 http://dx.doi.org/10.1120/jacmp.v15i1.4600 Text en © 2014 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
Riegel, Adam C.
Bucci, M. Kara
Mawlawi, Osama R.
Ahmad, Moiz
Luo, Dershan
Chandler, Adam
Pan, Tinsu
Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors
title Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors
title_full Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors
title_fullStr Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors
title_full_unstemmed Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors
title_short Defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors
title_sort defining internal target volume using positron emission tomography for radiation therapy planning of moving lung tumors
topic Radiation Oncology Physics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711243/
https://www.ncbi.nlm.nih.gov/pubmed/24423860
http://dx.doi.org/10.1120/jacmp.v15i1.4600
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