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Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI
PURPOSE: To compare the conspicuity of malignant lesions between FDG PET/CT and a new simultaneous, time-of-flight (TOF) enabled PET/MRI scanner. METHODS: All patients underwent a single-injection of FDG, followed by a dual imaging protocol consisting of PET/CT followed by TOF PET/MRI. PET/CT and PE...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245859/ https://www.ncbi.nlm.nih.gov/pubmed/28103230 http://dx.doi.org/10.1371/journal.pone.0167262 |
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author | Minamimoto, Ryogo Iagaru, Andrei Jamali, Mehran Holley, Dawn Barkhodari, Amir Vasanawala, Shreyas Zaharchuk, Greg |
author_facet | Minamimoto, Ryogo Iagaru, Andrei Jamali, Mehran Holley, Dawn Barkhodari, Amir Vasanawala, Shreyas Zaharchuk, Greg |
author_sort | Minamimoto, Ryogo |
collection | PubMed |
description | PURPOSE: To compare the conspicuity of malignant lesions between FDG PET/CT and a new simultaneous, time-of-flight (TOF) enabled PET/MRI scanner. METHODS: All patients underwent a single-injection of FDG, followed by a dual imaging protocol consisting of PET/CT followed by TOF PET/MRI. PET/CT and PET/MRI images were evaluated by two readers independently for areas of FDG uptake compatible with malignancy, and then categorized into 5 groups (1: PET/MRI and PET/CT positive; 2: PET/MRI positive, PET/CT positive in retrospect; 3: PET/CT positive, PET/MRI positive in retrospect; 4: PET/MRI positive, PET/CT negative; 5: PET/MRI negative, PET/CT positive) by consensus. Patients with no lesions on either study or greater than 10 lesions based on either modality were excluded from the study. RESULTS: Fifty-two patients (mean±SD age: 58±14 years) underwent the dual imaging protocol; of these, 29 patients with a total of 93 FDG-avid lesions met the inclusion criteria. The majority of lesions (56%) were recorded prospectively in the same location on PET/CT and PET/MRI. About an equal small fraction of lesions were seen on PET/CT but only retrospectively on PET/MRI (9%) and vice versa (12%). More lesions were identified only on PET/MRI but not on PET/CT, even in retrospect (96% vs. 81%, respectively; p = 0.003). Discrepant lesions had lower maximum standardized uptake value (SUV(max)) than concordant lesions on both modalities (p<0.001). CONCLUSIONS: While most lesions were identified prospectively on both modalities, significantly more lesions were identified with PET/MRI than with PET/CT. |
format | Online Article Text |
id | pubmed-5245859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52458592017-02-06 Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI Minamimoto, Ryogo Iagaru, Andrei Jamali, Mehran Holley, Dawn Barkhodari, Amir Vasanawala, Shreyas Zaharchuk, Greg PLoS One Research Article PURPOSE: To compare the conspicuity of malignant lesions between FDG PET/CT and a new simultaneous, time-of-flight (TOF) enabled PET/MRI scanner. METHODS: All patients underwent a single-injection of FDG, followed by a dual imaging protocol consisting of PET/CT followed by TOF PET/MRI. PET/CT and PET/MRI images were evaluated by two readers independently for areas of FDG uptake compatible with malignancy, and then categorized into 5 groups (1: PET/MRI and PET/CT positive; 2: PET/MRI positive, PET/CT positive in retrospect; 3: PET/CT positive, PET/MRI positive in retrospect; 4: PET/MRI positive, PET/CT negative; 5: PET/MRI negative, PET/CT positive) by consensus. Patients with no lesions on either study or greater than 10 lesions based on either modality were excluded from the study. RESULTS: Fifty-two patients (mean±SD age: 58±14 years) underwent the dual imaging protocol; of these, 29 patients with a total of 93 FDG-avid lesions met the inclusion criteria. The majority of lesions (56%) were recorded prospectively in the same location on PET/CT and PET/MRI. About an equal small fraction of lesions were seen on PET/CT but only retrospectively on PET/MRI (9%) and vice versa (12%). More lesions were identified only on PET/MRI but not on PET/CT, even in retrospect (96% vs. 81%, respectively; p = 0.003). Discrepant lesions had lower maximum standardized uptake value (SUV(max)) than concordant lesions on both modalities (p<0.001). CONCLUSIONS: While most lesions were identified prospectively on both modalities, significantly more lesions were identified with PET/MRI than with PET/CT. Public Library of Science 2017-01-19 /pmc/articles/PMC5245859/ /pubmed/28103230 http://dx.doi.org/10.1371/journal.pone.0167262 Text en © 2017 Minamimoto 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 Minamimoto, Ryogo Iagaru, Andrei Jamali, Mehran Holley, Dawn Barkhodari, Amir Vasanawala, Shreyas Zaharchuk, Greg Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI |
title | Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI |
title_full | Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI |
title_fullStr | Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI |
title_full_unstemmed | Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI |
title_short | Conspicuity of Malignant Lesions on PET/CT and Simultaneous Time-Of-Flight PET/MRI |
title_sort | conspicuity of malignant lesions on pet/ct and simultaneous time-of-flight pet/mri |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245859/ https://www.ncbi.nlm.nih.gov/pubmed/28103230 http://dx.doi.org/10.1371/journal.pone.0167262 |
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