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Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions
Lung cancer, the most commonly diagnosed cancer worldwide, usually presents as solid pulmonary nodules (SPNs) on early diagnostic images. Classification of malignant disease at this early timepoint is critical for improving the success of surgical resection and increasing 5-year survival rates. (18)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571049/ https://www.ncbi.nlm.nih.gov/pubmed/28839156 http://dx.doi.org/10.1038/s41598-017-08764-7 |
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author | Chen, Song Harmon, Stephanie Perk, Timothy Li, Xuena Chen, Meijie Li, Yaming Jeraj, Robert |
author_facet | Chen, Song Harmon, Stephanie Perk, Timothy Li, Xuena Chen, Meijie Li, Yaming Jeraj, Robert |
author_sort | Chen, Song |
collection | PubMed |
description | Lung cancer, the most commonly diagnosed cancer worldwide, usually presents as solid pulmonary nodules (SPNs) on early diagnostic images. Classification of malignant disease at this early timepoint is critical for improving the success of surgical resection and increasing 5-year survival rates. (18)F-fluorodeoxyglucose ((18)F-FDG) PET/CT has demonstrated value for SPNs diagnosis with high sensitivity to detect malignant SPNs, but lower specificity in diagnosing malignant SPNs in populations with endemic infectious lung disease. This study aimed to determine whether quantitative heterogeneity derived from various texture features on dual time FDG PET/CT images (DTPI) can differentiate between malignant and benign SPNs in patients from granuloma-endemic regions. Machine learning methods were employed to find optimal discrimination between malignant and benign nodules. Machine learning models trained by texture features on DTPI images achieved significant improvements over standard clinical metrics and visual interpretation for discriminating benign from malignant SPNs, especially by texture features on delayed FDG PET/CT images. |
format | Online Article Text |
id | pubmed-5571049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55710492017-09-01 Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions Chen, Song Harmon, Stephanie Perk, Timothy Li, Xuena Chen, Meijie Li, Yaming Jeraj, Robert Sci Rep Article Lung cancer, the most commonly diagnosed cancer worldwide, usually presents as solid pulmonary nodules (SPNs) on early diagnostic images. Classification of malignant disease at this early timepoint is critical for improving the success of surgical resection and increasing 5-year survival rates. (18)F-fluorodeoxyglucose ((18)F-FDG) PET/CT has demonstrated value for SPNs diagnosis with high sensitivity to detect malignant SPNs, but lower specificity in diagnosing malignant SPNs in populations with endemic infectious lung disease. This study aimed to determine whether quantitative heterogeneity derived from various texture features on dual time FDG PET/CT images (DTPI) can differentiate between malignant and benign SPNs in patients from granuloma-endemic regions. Machine learning methods were employed to find optimal discrimination between malignant and benign nodules. Machine learning models trained by texture features on DTPI images achieved significant improvements over standard clinical metrics and visual interpretation for discriminating benign from malignant SPNs, especially by texture features on delayed FDG PET/CT images. Nature Publishing Group UK 2017-08-24 /pmc/articles/PMC5571049/ /pubmed/28839156 http://dx.doi.org/10.1038/s41598-017-08764-7 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Song Harmon, Stephanie Perk, Timothy Li, Xuena Chen, Meijie Li, Yaming Jeraj, Robert Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions |
title | Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions |
title_full | Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions |
title_fullStr | Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions |
title_full_unstemmed | Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions |
title_short | Diagnostic classification of solitary pulmonary nodules using dual time (18)F-FDG PET/CT image texture features in granuloma-endemic regions |
title_sort | diagnostic classification of solitary pulmonary nodules using dual time (18)f-fdg pet/ct image texture features in granuloma-endemic regions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571049/ https://www.ncbi.nlm.nih.gov/pubmed/28839156 http://dx.doi.org/10.1038/s41598-017-08764-7 |
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