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Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography?

Correct staging is the most crucial for the treatment outcome in cancer management. Molecular imaging with (18)F-fluoroestradiol (FES) positron emission tomography-computed tomography (PET-CT) targets estrogen receptor (ER) and may have a higher incremental value in diagnosis by aiding specificity....

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Autores principales: Gupta, Manoj, Datta, Anupama, Choudhury, Partha S., Dsouza, Maria, Batra, Ullas, Mishra, Anil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436319/
https://www.ncbi.nlm.nih.gov/pubmed/28553180
http://dx.doi.org/10.4103/1450-1147.203071
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author Gupta, Manoj
Datta, Anupama
Choudhury, Partha S.
Dsouza, Maria
Batra, Ullas
Mishra, Anil
author_facet Gupta, Manoj
Datta, Anupama
Choudhury, Partha S.
Dsouza, Maria
Batra, Ullas
Mishra, Anil
author_sort Gupta, Manoj
collection PubMed
description Correct staging is the most crucial for the treatment outcome in cancer management. Molecular imaging with (18)F-fluoroestradiol (FES) positron emission tomography-computed tomography (PET-CT) targets estrogen receptor (ER) and may have a higher incremental value in diagnosis by aiding specificity. We enrolled 12 female breast cancer patients prospectively and did (18)F-FES PET-CT and (18)F-fluorodeoxyglucose (FDG) PET-CT within 1 week interval time. Lesion detection sensitivity was compared for a total number of lesions and for nonhepatic lesions only by McNemar test. (18)F-FES PET-CT was taken as reference in case of indeterminate lesions. The incremental value reported by identifying (18)F-FES exclusive lesions and by characterization of (18)F-FDG indeterminate lesions. Spearman rank test was used to correlate ER expression and maximum standardized uptake value (SUVmax). Two ER-negative patients with no (18)F-FES uptake were excluded. Ten ER-positive patients with 154 disease lesions were finally analyzed. (18)F-FDG picked-up 142 lesions (sensitivity 92.21%), whereas (18)F-FES picked-up 116 lesions (sensitivity 75.32%) and this difference was statistically significant. For nonhepatic lesions (n = 136) detectability, (18)F-FDG picked-up 124 (sensitivity 91.18%), whereas (18)F-FES picked-up 116 (sensitivity 85.29%) lesions and this difference was not statistically significant. Beside 12 exclusive lesions, (18)F-FES characterized 41 (27.5%) (18)F-FDG indeterminate lesions. Overall (18)F-FES impacted 20% patient management. The positive trend was also seen with (18)F-FES SUVmax with ER expression and negative with (18)F-FDG SUVmax. We conclude, (18)F-FDG has overall better sensitivity than (18)F-FES PET-CT, however for nonhepatic metastasis difference was not significant. (18)F-FES PET-CT better-characterized lesions and impacted 20% patient management. Therefore, (18)F-FES PET-CT should be used with (18)F-FDG PET-CT in strongly ER expressing patients for better specificity.
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spelling pubmed-54363192017-05-26 Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography? Gupta, Manoj Datta, Anupama Choudhury, Partha S. Dsouza, Maria Batra, Ullas Mishra, Anil World J Nucl Med Original Article Correct staging is the most crucial for the treatment outcome in cancer management. Molecular imaging with (18)F-fluoroestradiol (FES) positron emission tomography-computed tomography (PET-CT) targets estrogen receptor (ER) and may have a higher incremental value in diagnosis by aiding specificity. We enrolled 12 female breast cancer patients prospectively and did (18)F-FES PET-CT and (18)F-fluorodeoxyglucose (FDG) PET-CT within 1 week interval time. Lesion detection sensitivity was compared for a total number of lesions and for nonhepatic lesions only by McNemar test. (18)F-FES PET-CT was taken as reference in case of indeterminate lesions. The incremental value reported by identifying (18)F-FES exclusive lesions and by characterization of (18)F-FDG indeterminate lesions. Spearman rank test was used to correlate ER expression and maximum standardized uptake value (SUVmax). Two ER-negative patients with no (18)F-FES uptake were excluded. Ten ER-positive patients with 154 disease lesions were finally analyzed. (18)F-FDG picked-up 142 lesions (sensitivity 92.21%), whereas (18)F-FES picked-up 116 lesions (sensitivity 75.32%) and this difference was statistically significant. For nonhepatic lesions (n = 136) detectability, (18)F-FDG picked-up 124 (sensitivity 91.18%), whereas (18)F-FES picked-up 116 (sensitivity 85.29%) lesions and this difference was not statistically significant. Beside 12 exclusive lesions, (18)F-FES characterized 41 (27.5%) (18)F-FDG indeterminate lesions. Overall (18)F-FES impacted 20% patient management. The positive trend was also seen with (18)F-FES SUVmax with ER expression and negative with (18)F-FDG SUVmax. We conclude, (18)F-FDG has overall better sensitivity than (18)F-FES PET-CT, however for nonhepatic metastasis difference was not significant. (18)F-FES PET-CT better-characterized lesions and impacted 20% patient management. Therefore, (18)F-FES PET-CT should be used with (18)F-FDG PET-CT in strongly ER expressing patients for better specificity. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5436319/ /pubmed/28553180 http://dx.doi.org/10.4103/1450-1147.203071 Text en Copyright: © 2017 World Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Gupta, Manoj
Datta, Anupama
Choudhury, Partha S.
Dsouza, Maria
Batra, Ullas
Mishra, Anil
Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography?
title Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography?
title_full Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography?
title_fullStr Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography?
title_full_unstemmed Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography?
title_short Can (18)F-Fluoroestradiol Positron Emission Tomography Become a New Imaging Standard in the Estrogen Receptor-positive Breast Cancer Patient: A Prospective Comparative Study with (18)F-Fluorodeoxyglucose Positron Emission Tomography?
title_sort can (18)f-fluoroestradiol positron emission tomography become a new imaging standard in the estrogen receptor-positive breast cancer patient: a prospective comparative study with (18)f-fluorodeoxyglucose positron emission tomography?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436319/
https://www.ncbi.nlm.nih.gov/pubmed/28553180
http://dx.doi.org/10.4103/1450-1147.203071
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