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Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI

In the context of brain tumour response assessment, deep learning-based three-dimensional (3D) tumour segmentation has shown potential to enter the routine radiological workflow. The purpose of the present study was to perform an external evaluation of a state-of-the-art deep learning 3D brain tumou...

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Autores principales: Sørensen, Peter Jagd, Carlsen, Jonathan Frederik, Larsen, Vibeke Andrée, Andersen, Flemming Littrup, Ladefoged, Claes Nøhr, Nielsen, Michael Bachmann, Poulsen, Hans Skovgaard, Hansen, Adam Espe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9914320/
https://www.ncbi.nlm.nih.gov/pubmed/36766468
http://dx.doi.org/10.3390/diagnostics13030363
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author Sørensen, Peter Jagd
Carlsen, Jonathan Frederik
Larsen, Vibeke Andrée
Andersen, Flemming Littrup
Ladefoged, Claes Nøhr
Nielsen, Michael Bachmann
Poulsen, Hans Skovgaard
Hansen, Adam Espe
author_facet Sørensen, Peter Jagd
Carlsen, Jonathan Frederik
Larsen, Vibeke Andrée
Andersen, Flemming Littrup
Ladefoged, Claes Nøhr
Nielsen, Michael Bachmann
Poulsen, Hans Skovgaard
Hansen, Adam Espe
author_sort Sørensen, Peter Jagd
collection PubMed
description In the context of brain tumour response assessment, deep learning-based three-dimensional (3D) tumour segmentation has shown potential to enter the routine radiological workflow. The purpose of the present study was to perform an external evaluation of a state-of-the-art deep learning 3D brain tumour segmentation algorithm (HD-GLIO) on an independent cohort of consecutive, post-operative patients. For 66 consecutive magnetic resonance imaging examinations, we compared delineations of contrast-enhancing (CE) tumour lesions and non-enhancing T2/FLAIR hyperintense abnormality (NE) lesions by the HD-GLIO algorithm and radiologists using Dice similarity coefficients (Dice). Volume agreement was assessed using concordance correlation coefficients (CCCs) and Bland–Altman plots. The algorithm performed very well regarding the segmentation of NE volumes (median Dice = 0.79) and CE tumour volumes larger than 1.0 cm(3) (median Dice = 0.86). If considering all cases with CE tumour lesions, the performance dropped significantly (median Dice = 0.40). Volume agreement was excellent with CCCs of 0.997 (CE tumour volumes) and 0.922 (NE volumes). The findings have implications for the application of the HD-GLIO algorithm in the routine radiological workflow where small contrast-enhancing tumours will constitute a considerable share of the follow-up cases. Our study underlines that independent validations on clinical datasets are key to asserting the robustness of deep learning algorithms.
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spelling pubmed-99143202023-02-11 Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI Sørensen, Peter Jagd Carlsen, Jonathan Frederik Larsen, Vibeke Andrée Andersen, Flemming Littrup Ladefoged, Claes Nøhr Nielsen, Michael Bachmann Poulsen, Hans Skovgaard Hansen, Adam Espe Diagnostics (Basel) Article In the context of brain tumour response assessment, deep learning-based three-dimensional (3D) tumour segmentation has shown potential to enter the routine radiological workflow. The purpose of the present study was to perform an external evaluation of a state-of-the-art deep learning 3D brain tumour segmentation algorithm (HD-GLIO) on an independent cohort of consecutive, post-operative patients. For 66 consecutive magnetic resonance imaging examinations, we compared delineations of contrast-enhancing (CE) tumour lesions and non-enhancing T2/FLAIR hyperintense abnormality (NE) lesions by the HD-GLIO algorithm and radiologists using Dice similarity coefficients (Dice). Volume agreement was assessed using concordance correlation coefficients (CCCs) and Bland–Altman plots. The algorithm performed very well regarding the segmentation of NE volumes (median Dice = 0.79) and CE tumour volumes larger than 1.0 cm(3) (median Dice = 0.86). If considering all cases with CE tumour lesions, the performance dropped significantly (median Dice = 0.40). Volume agreement was excellent with CCCs of 0.997 (CE tumour volumes) and 0.922 (NE volumes). The findings have implications for the application of the HD-GLIO algorithm in the routine radiological workflow where small contrast-enhancing tumours will constitute a considerable share of the follow-up cases. Our study underlines that independent validations on clinical datasets are key to asserting the robustness of deep learning algorithms. MDPI 2023-01-18 /pmc/articles/PMC9914320/ /pubmed/36766468 http://dx.doi.org/10.3390/diagnostics13030363 Text en © 2023 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
Sørensen, Peter Jagd
Carlsen, Jonathan Frederik
Larsen, Vibeke Andrée
Andersen, Flemming Littrup
Ladefoged, Claes Nøhr
Nielsen, Michael Bachmann
Poulsen, Hans Skovgaard
Hansen, Adam Espe
Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI
title Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI
title_full Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI
title_fullStr Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI
title_full_unstemmed Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI
title_short Evaluation of the HD-GLIO Deep Learning Algorithm for Brain Tumour Segmentation on Postoperative MRI
title_sort evaluation of the hd-glio deep learning algorithm for brain tumour segmentation on postoperative mri
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9914320/
https://www.ncbi.nlm.nih.gov/pubmed/36766468
http://dx.doi.org/10.3390/diagnostics13030363
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