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Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study
Histopathological growth patterns (HGPs) are independent prognosticators for colorectal liver metastases (CRLM). Currently, HGPs are determined postoperatively. In this study, we evaluated radiomics for preoperative prediction of HGPs on computed tomography (CT), and its robustness to segmentation a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8510954/ https://www.ncbi.nlm.nih.gov/pubmed/34533669 http://dx.doi.org/10.1007/s10585-021-10119-6 |
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author | Starmans, Martijn P. A. Buisman, Florian E. Renckens, Michel Willemssen, François E. J. A. van der Voort, Sebastian R. Groot Koerkamp, Bas Grünhagen, Dirk J. Niessen, Wiro J. Vermeulen, Peter B. Verhoef, Cornelis Visser, Jacob J. Klein, Stefan |
author_facet | Starmans, Martijn P. A. Buisman, Florian E. Renckens, Michel Willemssen, François E. J. A. van der Voort, Sebastian R. Groot Koerkamp, Bas Grünhagen, Dirk J. Niessen, Wiro J. Vermeulen, Peter B. Verhoef, Cornelis Visser, Jacob J. Klein, Stefan |
author_sort | Starmans, Martijn P. A. |
collection | PubMed |
description | Histopathological growth patterns (HGPs) are independent prognosticators for colorectal liver metastases (CRLM). Currently, HGPs are determined postoperatively. In this study, we evaluated radiomics for preoperative prediction of HGPs on computed tomography (CT), and its robustness to segmentation and acquisition variations. Patients with pure HGPs [i.e. 100% desmoplastic (dHGP) or 100% replacement (rHGP)] and a CT-scan who were surgically treated at the Erasmus MC between 2003–2015 were included retrospectively. Each lesion was segmented by three clinicians and a convolutional neural network (CNN). A prediction model was created using 564 radiomics features and a combination of machine learning approaches by training on the clinician’s and testing on the unseen CNN segmentations. The intra-class correlation coefficient (ICC) was used to select features robust to segmentation variations; ComBat was used to harmonize for acquisition variations. Evaluation was performed through a 100 × random-split cross-validation. The study included 93 CRLM in 76 patients (48% dHGP; 52% rHGP). Despite substantial differences between the segmentations of the three clinicians and the CNN, the radiomics model had a mean area under the curve of 0.69. ICC-based feature selection or ComBat yielded no improvement. Concluding, the combination of a CNN for segmentation and radiomics for classification has potential for automatically distinguishing dHGPs from rHGP, and is robust to segmentation and acquisition variations. Pending further optimization, including extension to mixed HGPs, our model may serve as a preoperative addition to postoperative HGP assessment, enabling further exploitation of HGPs as a biomarker. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10585-021-10119-6. |
format | Online Article Text |
id | pubmed-8510954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-85109542021-10-27 Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study Starmans, Martijn P. A. Buisman, Florian E. Renckens, Michel Willemssen, François E. J. A. van der Voort, Sebastian R. Groot Koerkamp, Bas Grünhagen, Dirk J. Niessen, Wiro J. Vermeulen, Peter B. Verhoef, Cornelis Visser, Jacob J. Klein, Stefan Clin Exp Metastasis Research Paper Histopathological growth patterns (HGPs) are independent prognosticators for colorectal liver metastases (CRLM). Currently, HGPs are determined postoperatively. In this study, we evaluated radiomics for preoperative prediction of HGPs on computed tomography (CT), and its robustness to segmentation and acquisition variations. Patients with pure HGPs [i.e. 100% desmoplastic (dHGP) or 100% replacement (rHGP)] and a CT-scan who were surgically treated at the Erasmus MC between 2003–2015 were included retrospectively. Each lesion was segmented by three clinicians and a convolutional neural network (CNN). A prediction model was created using 564 radiomics features and a combination of machine learning approaches by training on the clinician’s and testing on the unseen CNN segmentations. The intra-class correlation coefficient (ICC) was used to select features robust to segmentation variations; ComBat was used to harmonize for acquisition variations. Evaluation was performed through a 100 × random-split cross-validation. The study included 93 CRLM in 76 patients (48% dHGP; 52% rHGP). Despite substantial differences between the segmentations of the three clinicians and the CNN, the radiomics model had a mean area under the curve of 0.69. ICC-based feature selection or ComBat yielded no improvement. Concluding, the combination of a CNN for segmentation and radiomics for classification has potential for automatically distinguishing dHGPs from rHGP, and is robust to segmentation and acquisition variations. Pending further optimization, including extension to mixed HGPs, our model may serve as a preoperative addition to postoperative HGP assessment, enabling further exploitation of HGPs as a biomarker. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10585-021-10119-6. Springer Netherlands 2021-09-17 2021 /pmc/articles/PMC8510954/ /pubmed/34533669 http://dx.doi.org/10.1007/s10585-021-10119-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Research Paper Starmans, Martijn P. A. Buisman, Florian E. Renckens, Michel Willemssen, François E. J. A. van der Voort, Sebastian R. Groot Koerkamp, Bas Grünhagen, Dirk J. Niessen, Wiro J. Vermeulen, Peter B. Verhoef, Cornelis Visser, Jacob J. Klein, Stefan Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study |
title | Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study |
title_full | Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study |
title_fullStr | Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study |
title_full_unstemmed | Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study |
title_short | Distinguishing pure histopathological growth patterns of colorectal liver metastases on CT using deep learning and radiomics: a pilot study |
title_sort | distinguishing pure histopathological growth patterns of colorectal liver metastases on ct using deep learning and radiomics: a pilot study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8510954/ https://www.ncbi.nlm.nih.gov/pubmed/34533669 http://dx.doi.org/10.1007/s10585-021-10119-6 |
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