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Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT

BACKGROUND: To determine PET/CT and PET/MR reproducibility and PET/MR repeatability of fluorine 18 fluorodeoxyglucose (FDG) uptake measurements in tumors in cancer patients. METHODS: This IRB approved prospective study was performed between October 2015 and February 2016 in consecutive patients who...

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Autores principales: Groshar, David, Bernstine, Hanna, Goldberg, Natalia, Nidam, Meital, Stein, Dan, Abadi-Korek, Ifat, Domachevsky, Liran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381130/
https://www.ncbi.nlm.nih.gov/pubmed/28381292
http://dx.doi.org/10.1186/s40644-017-0113-9
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author Groshar, David
Bernstine, Hanna
Goldberg, Natalia
Nidam, Meital
Stein, Dan
Abadi-Korek, Ifat
Domachevsky, Liran
author_facet Groshar, David
Bernstine, Hanna
Goldberg, Natalia
Nidam, Meital
Stein, Dan
Abadi-Korek, Ifat
Domachevsky, Liran
author_sort Groshar, David
collection PubMed
description BACKGROUND: To determine PET/CT and PET/MR reproducibility and PET/MR repeatability of fluorine 18 fluorodeoxyglucose (FDG) uptake measurements in tumors in cancer patients. METHODS: This IRB approved prospective study was performed between October 2015 and February 2016 in consecutive patients who performed same day PET/CT and two sequential PET/MR. Thirty three patients with visible tumors (N = 63) were included. SUV for body weight (SUV) and lean body mass (SUL) were obtained. Volume of interest (VOI) with a threshold of 40% was used and SUV/L’s, metabolic tumor volume (MTV) and tumor to liver ratio (T/L) were calculated. Measurements were plotted in a scattered diagram to visually identify correlation, a regression line was drawn and the equation of the line was calculated. Bland-Altman plots expressed as percentages were constructed to assess the agreement between measurements. The maximal clinically acceptable limits range was defined as ±30%. RESULTS: Lesional SUV’s, SUL’s and MTV corrected to body weight (BW) and lean body mass (LBM) demonstrated strong positive linear correlation between PET/CT and PET/MR and between two sequential PET/MR. The 95% limits of agreement ranged from -27.7 to 17.5 with a mean of -5.1 and -27.6 to 17.9 with a mean of -4.9 for SUVpeak and SULpeak, respectively for sequential PET/MR. Other PET metrics demonstrated limits range that is above ±30% between PET/CT and PET/MR and between two sequential PET/MR. CONCLUSION: PET/MR SUV/L peak has a clinically acceptable repeatability performance and can be used to evaluate the response to treatment.
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spelling pubmed-53811302017-04-10 Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT Groshar, David Bernstine, Hanna Goldberg, Natalia Nidam, Meital Stein, Dan Abadi-Korek, Ifat Domachevsky, Liran Cancer Imaging Research Article BACKGROUND: To determine PET/CT and PET/MR reproducibility and PET/MR repeatability of fluorine 18 fluorodeoxyglucose (FDG) uptake measurements in tumors in cancer patients. METHODS: This IRB approved prospective study was performed between October 2015 and February 2016 in consecutive patients who performed same day PET/CT and two sequential PET/MR. Thirty three patients with visible tumors (N = 63) were included. SUV for body weight (SUV) and lean body mass (SUL) were obtained. Volume of interest (VOI) with a threshold of 40% was used and SUV/L’s, metabolic tumor volume (MTV) and tumor to liver ratio (T/L) were calculated. Measurements were plotted in a scattered diagram to visually identify correlation, a regression line was drawn and the equation of the line was calculated. Bland-Altman plots expressed as percentages were constructed to assess the agreement between measurements. The maximal clinically acceptable limits range was defined as ±30%. RESULTS: Lesional SUV’s, SUL’s and MTV corrected to body weight (BW) and lean body mass (LBM) demonstrated strong positive linear correlation between PET/CT and PET/MR and between two sequential PET/MR. The 95% limits of agreement ranged from -27.7 to 17.5 with a mean of -5.1 and -27.6 to 17.9 with a mean of -4.9 for SUVpeak and SULpeak, respectively for sequential PET/MR. Other PET metrics demonstrated limits range that is above ±30% between PET/CT and PET/MR and between two sequential PET/MR. CONCLUSION: PET/MR SUV/L peak has a clinically acceptable repeatability performance and can be used to evaluate the response to treatment. BioMed Central 2017-04-05 /pmc/articles/PMC5381130/ /pubmed/28381292 http://dx.doi.org/10.1186/s40644-017-0113-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Groshar, David
Bernstine, Hanna
Goldberg, Natalia
Nidam, Meital
Stein, Dan
Abadi-Korek, Ifat
Domachevsky, Liran
Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT
title Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT
title_full Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT
title_fullStr Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT
title_full_unstemmed Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT
title_short Reproducibility and repeatability of same-day two sequential FDG PET/MR and PET/CT
title_sort reproducibility and repeatability of same-day two sequential fdg pet/mr and pet/ct
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381130/
https://www.ncbi.nlm.nih.gov/pubmed/28381292
http://dx.doi.org/10.1186/s40644-017-0113-9
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