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Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy

BACKGROUND AND PURPOSE: Anatomical changes during radiotherapy pose a challenge to robustness of plans. Principal component analysis (PCA) is commonly used to model such changes. We propose a toolbox to evaluate how closely a given PCA model can represent actual deformations seen in the patient and...

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Autores principales: Argota-Perez, Raul, Robbins, Jennifer, Green, Andrew, Herk, Marcel van, Korreman, Stine, Vásquez-Osorio, Eliana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038571/
https://www.ncbi.nlm.nih.gov/pubmed/35493853
http://dx.doi.org/10.1016/j.phro.2022.04.002
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author Argota-Perez, Raul
Robbins, Jennifer
Green, Andrew
Herk, Marcel van
Korreman, Stine
Vásquez-Osorio, Eliana
author_facet Argota-Perez, Raul
Robbins, Jennifer
Green, Andrew
Herk, Marcel van
Korreman, Stine
Vásquez-Osorio, Eliana
author_sort Argota-Perez, Raul
collection PubMed
description BACKGROUND AND PURPOSE: Anatomical changes during radiotherapy pose a challenge to robustness of plans. Principal component analysis (PCA) is commonly used to model such changes. We propose a toolbox to evaluate how closely a given PCA model can represent actual deformations seen in the patient and highlight regions where the model struggles to capture these changes. MATERIALS AND METHODS: We propose to calculate a residual error map from the difference between an actual displacement vector field (DVF) and the closest DVF that the PCA model can produce. This was done by taking the inner product of the DVF with the PCA components from the model. As a global measure of error, the 90th percentile of the residual errors [Formula: see text]) across the whole scan was used. As proof of principle, we demonstrated this approach on both patient-specific cases and a population-based PCA in head and neck (H&N) cancer patients. These models were created using deformation data from deformable registrations between the planning computed tomography and cone-beam computed tomography (CBCTs), and were evaluated against DVFs from registrations of CBCTs not used to create the model. RESULTS: For our example cases, the oropharyngeal and the nasal cavity regions showed the largest local residual error, indicating the PCA models struggle to predict deformations seen in these regions. [Formula: see text] ranged from 0.4 mm to 6.3 mm across the different models. CONCLUSIONS: A method to quantitatively evaluate how well PCA models represent observed anatomical changes was proposed. We demonstrated our approach on H&N PCA models, but it can be applied to other sites.
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spelling pubmed-90385712022-04-27 Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy Argota-Perez, Raul Robbins, Jennifer Green, Andrew Herk, Marcel van Korreman, Stine Vásquez-Osorio, Eliana Phys Imaging Radiat Oncol Original Research Article BACKGROUND AND PURPOSE: Anatomical changes during radiotherapy pose a challenge to robustness of plans. Principal component analysis (PCA) is commonly used to model such changes. We propose a toolbox to evaluate how closely a given PCA model can represent actual deformations seen in the patient and highlight regions where the model struggles to capture these changes. MATERIALS AND METHODS: We propose to calculate a residual error map from the difference between an actual displacement vector field (DVF) and the closest DVF that the PCA model can produce. This was done by taking the inner product of the DVF with the PCA components from the model. As a global measure of error, the 90th percentile of the residual errors [Formula: see text]) across the whole scan was used. As proof of principle, we demonstrated this approach on both patient-specific cases and a population-based PCA in head and neck (H&N) cancer patients. These models were created using deformation data from deformable registrations between the planning computed tomography and cone-beam computed tomography (CBCTs), and were evaluated against DVFs from registrations of CBCTs not used to create the model. RESULTS: For our example cases, the oropharyngeal and the nasal cavity regions showed the largest local residual error, indicating the PCA models struggle to predict deformations seen in these regions. [Formula: see text] ranged from 0.4 mm to 6.3 mm across the different models. CONCLUSIONS: A method to quantitatively evaluate how well PCA models represent observed anatomical changes was proposed. We demonstrated our approach on H&N PCA models, but it can be applied to other sites. Elsevier 2022-04-13 /pmc/articles/PMC9038571/ /pubmed/35493853 http://dx.doi.org/10.1016/j.phro.2022.04.002 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research Article
Argota-Perez, Raul
Robbins, Jennifer
Green, Andrew
Herk, Marcel van
Korreman, Stine
Vásquez-Osorio, Eliana
Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy
title Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy
title_full Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy
title_fullStr Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy
title_full_unstemmed Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy
title_short Evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy
title_sort evaluating principal component analysis models for representing anatomical changes in head and neck radiotherapy
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038571/
https://www.ncbi.nlm.nih.gov/pubmed/35493853
http://dx.doi.org/10.1016/j.phro.2022.04.002
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