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Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer

Application of textural features analysis to 18F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET) images has been used to characterize intra-tumor uptake heterogeneity and has been shown to reflect disease outcome. A current hypothesis is that (18)F-FDG uptake heterogeneity may refl...

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Autores principales: Tixier, Florent, Groves, Ashley M., Goh, Vicky, Hatt, Mathieu, Ingrand, Pierre, Le Rest, Catherine Cheze, Visvikis, Dimitris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057188/
https://www.ncbi.nlm.nih.gov/pubmed/24926986
http://dx.doi.org/10.1371/journal.pone.0099567
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author Tixier, Florent
Groves, Ashley M.
Goh, Vicky
Hatt, Mathieu
Ingrand, Pierre
Le Rest, Catherine Cheze
Visvikis, Dimitris
author_facet Tixier, Florent
Groves, Ashley M.
Goh, Vicky
Hatt, Mathieu
Ingrand, Pierre
Le Rest, Catherine Cheze
Visvikis, Dimitris
author_sort Tixier, Florent
collection PubMed
description Application of textural features analysis to 18F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET) images has been used to characterize intra-tumor uptake heterogeneity and has been shown to reflect disease outcome. A current hypothesis is that (18)F-FDG uptake heterogeneity may reflect the physiological tracer uptake related to tumor perfusion. The purpose of our study was to investigate the correlations between intra-tumor uptake heterogeneity and vascular parameters derived from dynamic contrast enhanced (DCE) computed tomography (CT) obtained from an integrated (18)F-FDG PET/perfusion CT examination. METHODS: Thirty patients with proven colorectal cancer prospectively underwent integrated (18)F-FDG PET/DCE-CT to assess the metabolic-flow phenotype. Both CT blood flow parametric maps and PET images were analyzed. Correlations between PET heterogeneity and perfusion CT were assessed by Spearman's rank correlation analysis. RESULTS: Blood flow visualization provided by DCE-CT images was significantly correlated with (18)F-FDG PET metabolically active tumor volume as well as with uptake heterogeneity for patients with stage III/IV tumors (|ρ|:0.66 to 0.78; p-value<0.02). CONCLUSION: The positive correlation found with tumor blood flow indicates that intra-tumor heterogeneity of (18)F-FDG PET accumulation reflects to some extent tracer distribution and consequently indicates that (18)F-FDG PET intra-tumor heterogeneity may be associated with physiological processes such as tumor vascularization.
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spelling pubmed-40571882014-06-18 Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer Tixier, Florent Groves, Ashley M. Goh, Vicky Hatt, Mathieu Ingrand, Pierre Le Rest, Catherine Cheze Visvikis, Dimitris PLoS One Research Article Application of textural features analysis to 18F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET) images has been used to characterize intra-tumor uptake heterogeneity and has been shown to reflect disease outcome. A current hypothesis is that (18)F-FDG uptake heterogeneity may reflect the physiological tracer uptake related to tumor perfusion. The purpose of our study was to investigate the correlations between intra-tumor uptake heterogeneity and vascular parameters derived from dynamic contrast enhanced (DCE) computed tomography (CT) obtained from an integrated (18)F-FDG PET/perfusion CT examination. METHODS: Thirty patients with proven colorectal cancer prospectively underwent integrated (18)F-FDG PET/DCE-CT to assess the metabolic-flow phenotype. Both CT blood flow parametric maps and PET images were analyzed. Correlations between PET heterogeneity and perfusion CT were assessed by Spearman's rank correlation analysis. RESULTS: Blood flow visualization provided by DCE-CT images was significantly correlated with (18)F-FDG PET metabolically active tumor volume as well as with uptake heterogeneity for patients with stage III/IV tumors (|ρ|:0.66 to 0.78; p-value<0.02). CONCLUSION: The positive correlation found with tumor blood flow indicates that intra-tumor heterogeneity of (18)F-FDG PET accumulation reflects to some extent tracer distribution and consequently indicates that (18)F-FDG PET intra-tumor heterogeneity may be associated with physiological processes such as tumor vascularization. Public Library of Science 2014-06-13 /pmc/articles/PMC4057188/ /pubmed/24926986 http://dx.doi.org/10.1371/journal.pone.0099567 Text en © 2014 Tixier 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tixier, Florent
Groves, Ashley M.
Goh, Vicky
Hatt, Mathieu
Ingrand, Pierre
Le Rest, Catherine Cheze
Visvikis, Dimitris
Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer
title Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer
title_full Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer
title_fullStr Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer
title_full_unstemmed Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer
title_short Correlation of Intra-Tumor (18)F-FDG Uptake Heterogeneity Indices with Perfusion CT Derived Parameters in Colorectal Cancer
title_sort correlation of intra-tumor (18)f-fdg uptake heterogeneity indices with perfusion ct derived parameters in colorectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057188/
https://www.ncbi.nlm.nih.gov/pubmed/24926986
http://dx.doi.org/10.1371/journal.pone.0099567
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