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Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma

Quantitative parametric images of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse gliomas could be used to improve glioma grading, tumour delineation or the assessment of the uptake distribution of this positron emission tomography tracer. In this study, several parametric images and tumour-...

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Autores principales: Koopman, Thomas, Verburg, Niels, Pouwels, Petra JW, Wesseling, Pieter, Hoekstra, Otto S, De Witt Hamer, Philip C, Lammertsma, Adriaan A, Yaqub, Maqsood, Boellaard, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074601/
https://www.ncbi.nlm.nih.gov/pubmed/31122112
http://dx.doi.org/10.1177/0271678X19851878
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author Koopman, Thomas
Verburg, Niels
Pouwels, Petra JW
Wesseling, Pieter
Hoekstra, Otto S
De Witt Hamer, Philip C
Lammertsma, Adriaan A
Yaqub, Maqsood
Boellaard, Ronald
author_facet Koopman, Thomas
Verburg, Niels
Pouwels, Petra JW
Wesseling, Pieter
Hoekstra, Otto S
De Witt Hamer, Philip C
Lammertsma, Adriaan A
Yaqub, Maqsood
Boellaard, Ronald
author_sort Koopman, Thomas
collection PubMed
description Quantitative parametric images of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse gliomas could be used to improve glioma grading, tumour delineation or the assessment of the uptake distribution of this positron emission tomography tracer. In this study, several parametric images and tumour-to-normal maps were compared in terms of accuracy of region averages (when compared to results from nonlinear regression of a reversible two-tissue compartment plasma input model) and image noise using 90 min of dynamic scan data acquired in seven patients with diffuse glioma. We included plasma input methods (the basis function implementation of the single-tissue compartment model, spectral analysis and Logan graphical analysis) and reference tissue methods (basis function implementations of the simplified reference tissue model, variations of the multilinear reference tissue model and non-invasive Logan graphical analysis) as well as tumour-to-normal ratio maps at three intervals. (Non-invasive) Logan graphical analysis provided volume of distribution maps and distribution volume ratio maps with the lowest level of noise, while the basis function implementations provided the best accuracy. Tumour-to-normal ratio maps provided better results if later interval times were used, i.e. 60–90 min instead of 20–40 min, leading to lower bias (2.9% vs. 10.8%, respectively) and less noise (12.8% vs. 14.4%).
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spelling pubmed-70746012020-03-24 Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma Koopman, Thomas Verburg, Niels Pouwels, Petra JW Wesseling, Pieter Hoekstra, Otto S De Witt Hamer, Philip C Lammertsma, Adriaan A Yaqub, Maqsood Boellaard, Ronald J Cereb Blood Flow Metab Original Articles Quantitative parametric images of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse gliomas could be used to improve glioma grading, tumour delineation or the assessment of the uptake distribution of this positron emission tomography tracer. In this study, several parametric images and tumour-to-normal maps were compared in terms of accuracy of region averages (when compared to results from nonlinear regression of a reversible two-tissue compartment plasma input model) and image noise using 90 min of dynamic scan data acquired in seven patients with diffuse glioma. We included plasma input methods (the basis function implementation of the single-tissue compartment model, spectral analysis and Logan graphical analysis) and reference tissue methods (basis function implementations of the simplified reference tissue model, variations of the multilinear reference tissue model and non-invasive Logan graphical analysis) as well as tumour-to-normal ratio maps at three intervals. (Non-invasive) Logan graphical analysis provided volume of distribution maps and distribution volume ratio maps with the lowest level of noise, while the basis function implementations provided the best accuracy. Tumour-to-normal ratio maps provided better results if later interval times were used, i.e. 60–90 min instead of 20–40 min, leading to lower bias (2.9% vs. 10.8%, respectively) and less noise (12.8% vs. 14.4%). SAGE Publications 2019-05-24 2020-04 /pmc/articles/PMC7074601/ /pubmed/31122112 http://dx.doi.org/10.1177/0271678X19851878 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Koopman, Thomas
Verburg, Niels
Pouwels, Petra JW
Wesseling, Pieter
Hoekstra, Otto S
De Witt Hamer, Philip C
Lammertsma, Adriaan A
Yaqub, Maqsood
Boellaard, Ronald
Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma
title Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma
title_full Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma
title_fullStr Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma
title_full_unstemmed Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma
title_short Quantitative parametric maps of O-(2-[(18)F]fluoroethyl)-L-tyrosine kinetics in diffuse glioma
title_sort quantitative parametric maps of o-(2-[(18)f]fluoroethyl)-l-tyrosine kinetics in diffuse glioma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074601/
https://www.ncbi.nlm.nih.gov/pubmed/31122112
http://dx.doi.org/10.1177/0271678X19851878
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