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Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma

In this work, we assess the reproducibility and prognostic value of CT-derived radiomic features for resectable pancreatic ductal adenocarcinoma (PDAC). Two radiologists contoured tumour regions on pre-operative CT of two cohorts from two institutions undergoing curative-intent surgical resection fo...

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Autores principales: Khalvati, Farzad, Zhang, Yucheng, Baig, Sameer, Lobo-Mueller, Edrise M., Karanicolas, Paul, Gallinger, Steven, Haider, Masoom A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443807/
https://www.ncbi.nlm.nih.gov/pubmed/30931954
http://dx.doi.org/10.1038/s41598-019-41728-7
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author Khalvati, Farzad
Zhang, Yucheng
Baig, Sameer
Lobo-Mueller, Edrise M.
Karanicolas, Paul
Gallinger, Steven
Haider, Masoom A.
author_facet Khalvati, Farzad
Zhang, Yucheng
Baig, Sameer
Lobo-Mueller, Edrise M.
Karanicolas, Paul
Gallinger, Steven
Haider, Masoom A.
author_sort Khalvati, Farzad
collection PubMed
description In this work, we assess the reproducibility and prognostic value of CT-derived radiomic features for resectable pancreatic ductal adenocarcinoma (PDAC). Two radiologists contoured tumour regions on pre-operative CT of two cohorts from two institutions undergoing curative-intent surgical resection for PDAC. The first (n = 30) and second cohorts (n = 68) were used for training and validation of proposed prognostic model for overall survival (OS), respectively. Radiomic features were extracted using PyRadiomics library and those with weak inter-reader reproducibility were excluded. Through Cox regression models, significant features were identified in the training cohort and retested in the validation cohort. Significant features were then fused via Cox regression to build a single radiomic signature in the training cohort, which was validated across readers in the validation cohort. Two radiomic features derived from Sum Entropy and Cluster Tendency features were both robust to inter-reader reproducibility and prognostic of OS across cohorts and readers. The radiomic signature showed prognostic value for OS in the validation cohort with hazard ratios of 1.56 (P = 0.005) and 1.35 (P = 0.022), for the first and second reader, respectively. CT-based radiomic features were shown to be prognostic in patients with resectable PDAC. These features may help stratify patients for neoadjuvant or alternative therapies.
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spelling pubmed-64438072019-04-05 Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma Khalvati, Farzad Zhang, Yucheng Baig, Sameer Lobo-Mueller, Edrise M. Karanicolas, Paul Gallinger, Steven Haider, Masoom A. Sci Rep Article In this work, we assess the reproducibility and prognostic value of CT-derived radiomic features for resectable pancreatic ductal adenocarcinoma (PDAC). Two radiologists contoured tumour regions on pre-operative CT of two cohorts from two institutions undergoing curative-intent surgical resection for PDAC. The first (n = 30) and second cohorts (n = 68) were used for training and validation of proposed prognostic model for overall survival (OS), respectively. Radiomic features were extracted using PyRadiomics library and those with weak inter-reader reproducibility were excluded. Through Cox regression models, significant features were identified in the training cohort and retested in the validation cohort. Significant features were then fused via Cox regression to build a single radiomic signature in the training cohort, which was validated across readers in the validation cohort. Two radiomic features derived from Sum Entropy and Cluster Tendency features were both robust to inter-reader reproducibility and prognostic of OS across cohorts and readers. The radiomic signature showed prognostic value for OS in the validation cohort with hazard ratios of 1.56 (P = 0.005) and 1.35 (P = 0.022), for the first and second reader, respectively. CT-based radiomic features were shown to be prognostic in patients with resectable PDAC. These features may help stratify patients for neoadjuvant or alternative therapies. Nature Publishing Group UK 2019-04-01 /pmc/articles/PMC6443807/ /pubmed/30931954 http://dx.doi.org/10.1038/s41598-019-41728-7 Text en © The Author(s) 2019 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
Khalvati, Farzad
Zhang, Yucheng
Baig, Sameer
Lobo-Mueller, Edrise M.
Karanicolas, Paul
Gallinger, Steven
Haider, Masoom A.
Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma
title Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma
title_full Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma
title_fullStr Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma
title_full_unstemmed Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma
title_short Prognostic Value of CT Radiomic Features in Resectable Pancreatic Ductal Adenocarcinoma
title_sort prognostic value of ct radiomic features in resectable pancreatic ductal adenocarcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443807/
https://www.ncbi.nlm.nih.gov/pubmed/30931954
http://dx.doi.org/10.1038/s41598-019-41728-7
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