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Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors

Quantitative radiomic and iodine imaging features have been explored for diagnosis and characterization of tumors. In this work, we invistigate combined whole-lesion radiomic and iodine analysis for the differentiation of pulmonary tumors on contrast-enhanced dual-energy CT (DECT) chest images. 100...

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Autores principales: Azour, Lea, Ko, Jane P., O’Donnell, Thomas, Patel, Nihal, Bhattacharji, Priya, Moore, William H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276812/
https://www.ncbi.nlm.nih.gov/pubmed/35821374
http://dx.doi.org/10.1038/s41598-022-15351-y
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author Azour, Lea
Ko, Jane P.
O’Donnell, Thomas
Patel, Nihal
Bhattacharji, Priya
Moore, William H.
author_facet Azour, Lea
Ko, Jane P.
O’Donnell, Thomas
Patel, Nihal
Bhattacharji, Priya
Moore, William H.
author_sort Azour, Lea
collection PubMed
description Quantitative radiomic and iodine imaging features have been explored for diagnosis and characterization of tumors. In this work, we invistigate combined whole-lesion radiomic and iodine analysis for the differentiation of pulmonary tumors on contrast-enhanced dual-energy CT (DECT) chest images. 100 biopsy-proven solid lung lesions on contrast-enhanced DECT chest exams within 3 months of histopathologic sampling were identified. Lesions were volumetrically segmented using open-source software. Lesion segmentations and iodine density volumes were loaded into a radiomics prototype for quantitative analysis. Univariate analysis was performed to determine differences in volumetric iodine concentration (mean, median, maximum, minimum, 10th percentile, 90th percentile) and first and higher order radiomic features (n = 1212) between pulmonary tumors. Analyses were performed using a 2-sample t test, and filtered for false discoveries using Benjamini–Hochberg method. 100 individuals (mean age 65 ± 13 years; 59 women) with 64 primary and 36 metastatic lung lesions were included. Only one iodine concentration parameter, absolute minimum iodine, significantly differed between primary and metastatic pulmonary tumors (FDR-adjusted p = 0.015, AUC 0.69). 310 (FDR-adjusted p = 0.0008 to p = 0.0491) radiomic features differed between primary and metastatic lung tumors. Of these, 21 features achieved AUC ≥ 0.75. In subset analyses of lesions imaged by non-CTPA protocol (n = 72), 191 features significantly differed between primary and metastatic tumors, 19 of which achieved AUC ≥ 0.75. In subset analysis of tumors without history of prior treatment (n = 59), 40 features significantly differed between primary and metastatic tumors, 11 of which achieved AUC ≥ 0.75. Volumetric radiomic analysis provides differentiating capability beyond iodine quantification. While a high number of radiomic features differentiated primary versus metastatic pulmonary tumors, fewer features demonstrated good individual discriminatory utility.
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spelling pubmed-92768122022-07-14 Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors Azour, Lea Ko, Jane P. O’Donnell, Thomas Patel, Nihal Bhattacharji, Priya Moore, William H. Sci Rep Article Quantitative radiomic and iodine imaging features have been explored for diagnosis and characterization of tumors. In this work, we invistigate combined whole-lesion radiomic and iodine analysis for the differentiation of pulmonary tumors on contrast-enhanced dual-energy CT (DECT) chest images. 100 biopsy-proven solid lung lesions on contrast-enhanced DECT chest exams within 3 months of histopathologic sampling were identified. Lesions were volumetrically segmented using open-source software. Lesion segmentations and iodine density volumes were loaded into a radiomics prototype for quantitative analysis. Univariate analysis was performed to determine differences in volumetric iodine concentration (mean, median, maximum, minimum, 10th percentile, 90th percentile) and first and higher order radiomic features (n = 1212) between pulmonary tumors. Analyses were performed using a 2-sample t test, and filtered for false discoveries using Benjamini–Hochberg method. 100 individuals (mean age 65 ± 13 years; 59 women) with 64 primary and 36 metastatic lung lesions were included. Only one iodine concentration parameter, absolute minimum iodine, significantly differed between primary and metastatic pulmonary tumors (FDR-adjusted p = 0.015, AUC 0.69). 310 (FDR-adjusted p = 0.0008 to p = 0.0491) radiomic features differed between primary and metastatic lung tumors. Of these, 21 features achieved AUC ≥ 0.75. In subset analyses of lesions imaged by non-CTPA protocol (n = 72), 191 features significantly differed between primary and metastatic tumors, 19 of which achieved AUC ≥ 0.75. In subset analysis of tumors without history of prior treatment (n = 59), 40 features significantly differed between primary and metastatic tumors, 11 of which achieved AUC ≥ 0.75. Volumetric radiomic analysis provides differentiating capability beyond iodine quantification. While a high number of radiomic features differentiated primary versus metastatic pulmonary tumors, fewer features demonstrated good individual discriminatory utility. Nature Publishing Group UK 2022-07-12 /pmc/articles/PMC9276812/ /pubmed/35821374 http://dx.doi.org/10.1038/s41598-022-15351-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Azour, Lea
Ko, Jane P.
O’Donnell, Thomas
Patel, Nihal
Bhattacharji, Priya
Moore, William H.
Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors
title Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors
title_full Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors
title_fullStr Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors
title_full_unstemmed Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors
title_short Combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors
title_sort combined whole-lesion radiomic and iodine analysis for differentiation of pulmonary tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276812/
https://www.ncbi.nlm.nih.gov/pubmed/35821374
http://dx.doi.org/10.1038/s41598-022-15351-y
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