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Adding the temporal domain to PET radiomic features

BACKGROUND: Radiomic features, extracted from positron emission tomography, aim to characterize tumour biology based on tracer intensity, tumour geometry and/or tracer uptake heterogeneity. Currently, radiomic features are derived from static images. However, temporal changes in tracer uptake might...

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Autores principales: Noortman, Wyanne A., Vriens, Dennis, Slump, Cornelis H., Bussink, Johan, Meijer, Tineke W. H., de Geus-Oei, Lioe-Fee, van Velden, Floris H. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510999/
https://www.ncbi.nlm.nih.gov/pubmed/32966313
http://dx.doi.org/10.1371/journal.pone.0239438
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author Noortman, Wyanne A.
Vriens, Dennis
Slump, Cornelis H.
Bussink, Johan
Meijer, Tineke W. H.
de Geus-Oei, Lioe-Fee
van Velden, Floris H. P.
author_facet Noortman, Wyanne A.
Vriens, Dennis
Slump, Cornelis H.
Bussink, Johan
Meijer, Tineke W. H.
de Geus-Oei, Lioe-Fee
van Velden, Floris H. P.
author_sort Noortman, Wyanne A.
collection PubMed
description BACKGROUND: Radiomic features, extracted from positron emission tomography, aim to characterize tumour biology based on tracer intensity, tumour geometry and/or tracer uptake heterogeneity. Currently, radiomic features are derived from static images. However, temporal changes in tracer uptake might reveal new aspects of tumour biology. This study aims to explore additional information of these novel dynamic radiomic features compared to those derived from static or metabolic rate images. METHODS: Thirty-five patients with non-small cell lung carcinoma underwent dynamic [(18)F]FDG PET/CT scans. Spatial intensity, shape and texture radiomic features were derived from volumes of interest delineated on static PET and parametric metabolic rate PET. Dynamic grey level cooccurrence matrix (GLCM) and grey level run length matrix (GLRLM) features, assessing the temporal domain unidirectionally, were calculated on eight and sixteen time frames of equal length. Spearman’s rank correlations of parametric and dynamic features with static features were calculated to identify features with potential additional information. Survival analysis was performed for the non-redundant temporal features and a selection of static features using Kaplan-Meier analysis. RESULTS: Three out of 90 parametric features showed moderate correlations with corresponding static features (ρ≥0.61), all other features showed high correlations (ρ>0.7). Dynamic features are robust independent of frame duration. Five out of 22 dynamic GLCM features showed a negligible to moderate correlation with any static feature, suggesting additional information. All sixteen dynamic GLRLM features showed high correlations with static features, implying redundancy. Log-rank analyses of Kaplan-Meier survival curves for all features dichotomised at the median were insignificant. CONCLUSION: This study suggests that, compared to static features, some dynamic GLCM radiomic features show different information, whereas parametric features provide minimal additional information. Future studies should be conducted in larger populations to assess whether there is a clinical benefit of radiomics using the temporal domain over traditional radiomics.
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spelling pubmed-75109992020-10-01 Adding the temporal domain to PET radiomic features Noortman, Wyanne A. Vriens, Dennis Slump, Cornelis H. Bussink, Johan Meijer, Tineke W. H. de Geus-Oei, Lioe-Fee van Velden, Floris H. P. PLoS One Research Article BACKGROUND: Radiomic features, extracted from positron emission tomography, aim to characterize tumour biology based on tracer intensity, tumour geometry and/or tracer uptake heterogeneity. Currently, radiomic features are derived from static images. However, temporal changes in tracer uptake might reveal new aspects of tumour biology. This study aims to explore additional information of these novel dynamic radiomic features compared to those derived from static or metabolic rate images. METHODS: Thirty-five patients with non-small cell lung carcinoma underwent dynamic [(18)F]FDG PET/CT scans. Spatial intensity, shape and texture radiomic features were derived from volumes of interest delineated on static PET and parametric metabolic rate PET. Dynamic grey level cooccurrence matrix (GLCM) and grey level run length matrix (GLRLM) features, assessing the temporal domain unidirectionally, were calculated on eight and sixteen time frames of equal length. Spearman’s rank correlations of parametric and dynamic features with static features were calculated to identify features with potential additional information. Survival analysis was performed for the non-redundant temporal features and a selection of static features using Kaplan-Meier analysis. RESULTS: Three out of 90 parametric features showed moderate correlations with corresponding static features (ρ≥0.61), all other features showed high correlations (ρ>0.7). Dynamic features are robust independent of frame duration. Five out of 22 dynamic GLCM features showed a negligible to moderate correlation with any static feature, suggesting additional information. All sixteen dynamic GLRLM features showed high correlations with static features, implying redundancy. Log-rank analyses of Kaplan-Meier survival curves for all features dichotomised at the median were insignificant. CONCLUSION: This study suggests that, compared to static features, some dynamic GLCM radiomic features show different information, whereas parametric features provide minimal additional information. Future studies should be conducted in larger populations to assess whether there is a clinical benefit of radiomics using the temporal domain over traditional radiomics. Public Library of Science 2020-09-23 /pmc/articles/PMC7510999/ /pubmed/32966313 http://dx.doi.org/10.1371/journal.pone.0239438 Text en © 2020 Noortman et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Noortman, Wyanne A.
Vriens, Dennis
Slump, Cornelis H.
Bussink, Johan
Meijer, Tineke W. H.
de Geus-Oei, Lioe-Fee
van Velden, Floris H. P.
Adding the temporal domain to PET radiomic features
title Adding the temporal domain to PET radiomic features
title_full Adding the temporal domain to PET radiomic features
title_fullStr Adding the temporal domain to PET radiomic features
title_full_unstemmed Adding the temporal domain to PET radiomic features
title_short Adding the temporal domain to PET radiomic features
title_sort adding the temporal domain to pet radiomic features
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510999/
https://www.ncbi.nlm.nih.gov/pubmed/32966313
http://dx.doi.org/10.1371/journal.pone.0239438
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