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Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study

We investigated the role of [(18)F]FDG positron emission tomography/computed tomography (PET/CT) in evaluating ground-glass nodules (GGNs) by visual analysis and tissue fraction correction. A total of 40 pathologically confirmed ≥1 cm GGNs were evaluated visually and semiquantitatively. [(18)F]FDG u...

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Autores principales: Song, Yun Hye, Moon, Jung Won, Kim, Yoo Na, Woo, Ji Young, Son, Hye Joo, Lee, Suk Hyun, Hwang, Hee Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140844/
https://www.ncbi.nlm.nih.gov/pubmed/35626447
http://dx.doi.org/10.3390/diagnostics12051292
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author Song, Yun Hye
Moon, Jung Won
Kim, Yoo Na
Woo, Ji Young
Son, Hye Joo
Lee, Suk Hyun
Hwang, Hee Sung
author_facet Song, Yun Hye
Moon, Jung Won
Kim, Yoo Na
Woo, Ji Young
Son, Hye Joo
Lee, Suk Hyun
Hwang, Hee Sung
author_sort Song, Yun Hye
collection PubMed
description We investigated the role of [(18)F]FDG positron emission tomography/computed tomography (PET/CT) in evaluating ground-glass nodules (GGNs) by visual analysis and tissue fraction correction. A total of 40 pathologically confirmed ≥1 cm GGNs were evaluated visually and semiquantitatively. [(18)F]FDG uptake of GGN distinct from background lung activity was considered positive in visual analysis. In semiquantitative analysis, we performed tissue fraction correction for the maximum standardized uptake value (SUV(max)) of GGN. Of the 40 GGNs, 25 (63%) were adenocarcinomas, 9 (23%) were minimally invasive adenocarcinomas (MIAs), and 6 (15%) were adenocarcinomas in situ (AIS). On visual analysis, adenocarcinoma showed the highest positivity rate among the three pathological groups (88%, 44%, and 17%, respectively). Both SUV(max) and tissue-fraction–corrected SUV(max) (SUV(maxTF)) were in the order of adenocarcinoma > MIA > AIS (p = 0.033 and 0.018, respectively). SUV(maxTF) was significantly higher than SUV(max) before correction (2.4 [1.9–3.0] vs. 1.3 [0.8–1.8], p < 0.001). When using a cutoff value of 2.5, the positivity rate of GGNs was significantly higher in SUV(maxTF) than in SUV(max) (50% vs. 5%, p < 0.001). The diagnostic sensitivity of [(18)F]FDG PET/CT in predicting the malignancy of lung GGN was improved by tissue fraction correction and visual analysis.
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spelling pubmed-91408442022-05-28 Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study Song, Yun Hye Moon, Jung Won Kim, Yoo Na Woo, Ji Young Son, Hye Joo Lee, Suk Hyun Hwang, Hee Sung Diagnostics (Basel) Article We investigated the role of [(18)F]FDG positron emission tomography/computed tomography (PET/CT) in evaluating ground-glass nodules (GGNs) by visual analysis and tissue fraction correction. A total of 40 pathologically confirmed ≥1 cm GGNs were evaluated visually and semiquantitatively. [(18)F]FDG uptake of GGN distinct from background lung activity was considered positive in visual analysis. In semiquantitative analysis, we performed tissue fraction correction for the maximum standardized uptake value (SUV(max)) of GGN. Of the 40 GGNs, 25 (63%) were adenocarcinomas, 9 (23%) were minimally invasive adenocarcinomas (MIAs), and 6 (15%) were adenocarcinomas in situ (AIS). On visual analysis, adenocarcinoma showed the highest positivity rate among the three pathological groups (88%, 44%, and 17%, respectively). Both SUV(max) and tissue-fraction–corrected SUV(max) (SUV(maxTF)) were in the order of adenocarcinoma > MIA > AIS (p = 0.033 and 0.018, respectively). SUV(maxTF) was significantly higher than SUV(max) before correction (2.4 [1.9–3.0] vs. 1.3 [0.8–1.8], p < 0.001). When using a cutoff value of 2.5, the positivity rate of GGNs was significantly higher in SUV(maxTF) than in SUV(max) (50% vs. 5%, p < 0.001). The diagnostic sensitivity of [(18)F]FDG PET/CT in predicting the malignancy of lung GGN was improved by tissue fraction correction and visual analysis. MDPI 2022-05-23 /pmc/articles/PMC9140844/ /pubmed/35626447 http://dx.doi.org/10.3390/diagnostics12051292 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Song, Yun Hye
Moon, Jung Won
Kim, Yoo Na
Woo, Ji Young
Son, Hye Joo
Lee, Suk Hyun
Hwang, Hee Sung
Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study
title Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study
title_full Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study
title_fullStr Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study
title_full_unstemmed Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study
title_short Tissue Fraction Correction and Visual Analysis Increase Diagnostic Sensitivity in Predicting Malignancy of Ground-Glass Nodules on [(18)F]FDG PET/CT: A Bicenter Retrospective Study
title_sort tissue fraction correction and visual analysis increase diagnostic sensitivity in predicting malignancy of ground-glass nodules on [(18)f]fdg pet/ct: a bicenter retrospective study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140844/
https://www.ncbi.nlm.nih.gov/pubmed/35626447
http://dx.doi.org/10.3390/diagnostics12051292
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