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A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++
OBJECTIVE: Radiomic and deep learning studies based on magnetic resonance imaging (MRI) of liver tumor are gradually increasing. Manual segmentation of normal hepatic tissue and tumor exhibits limitations. METHODS: 105 patients diagnosed with hepatocellular carcinoma were retrospectively studied bet...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623778/ https://www.ncbi.nlm.nih.gov/pubmed/37923988 http://dx.doi.org/10.1186/s12885-023-11432-x |
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author | Wang, Jing Peng, Yanyang Jing, Shi Han, Lujun Li, Tian Luo, Junpeng |
author_facet | Wang, Jing Peng, Yanyang Jing, Shi Han, Lujun Li, Tian Luo, Junpeng |
author_sort | Wang, Jing |
collection | PubMed |
description | OBJECTIVE: Radiomic and deep learning studies based on magnetic resonance imaging (MRI) of liver tumor are gradually increasing. Manual segmentation of normal hepatic tissue and tumor exhibits limitations. METHODS: 105 patients diagnosed with hepatocellular carcinoma were retrospectively studied between Jan 2015 and Dec 2020. The patients were divided into three sets: training (n = 83), validation (n = 11), and internal testing (n = 11). Additionally, 9 cases were included from the Cancer Imaging Archive as the external test set. Using the arterial phase and T2WI sequences, expert radiologists manually delineated all images. Using deep learning, liver tumors and liver segments were automatically segmented. A preliminary liver segmentation was performed using the UNet + + network, and the segmented liver mask was re-input as the input end into the UNet + + network to segment liver tumors. The false positivity rate was reduced using a threshold value in the liver tumor segmentation. To evaluate the segmentation results, we calculated the Dice similarity coefficient (DSC), average false positivity rate (AFPR), and delineation time. RESULTS: The average DSC of the liver in the validation and internal testing sets was 0.91 and 0.92, respectively. In the validation set, manual and automatic delineation took 182.9 and 2.2 s, respectively. On an average, manual and automatic delineation took 169.8 and 1.7 s, respectively. The average DSC of liver tumors was 0.612 and 0.687 in the validation and internal testing sets, respectively. The average time for manual and automatic delineation and AFPR in the internal testing set were 47.4 s, 2.9 s, and 1.4, respectively, and those in the external test set were 29.5 s, 4.2 s, and 1.6, respectively. CONCLUSION: UNet + + can automatically segment normal hepatic tissue and liver tumors based on MR images. It provides a methodological basis for the automated segmentation of liver tumors, improves the delineation efficiency, and meets the requirement of extraction set analysis of further radiomics and deep learning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11432-x. |
format | Online Article Text |
id | pubmed-10623778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106237782023-11-04 A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++ Wang, Jing Peng, Yanyang Jing, Shi Han, Lujun Li, Tian Luo, Junpeng BMC Cancer Research OBJECTIVE: Radiomic and deep learning studies based on magnetic resonance imaging (MRI) of liver tumor are gradually increasing. Manual segmentation of normal hepatic tissue and tumor exhibits limitations. METHODS: 105 patients diagnosed with hepatocellular carcinoma were retrospectively studied between Jan 2015 and Dec 2020. The patients were divided into three sets: training (n = 83), validation (n = 11), and internal testing (n = 11). Additionally, 9 cases were included from the Cancer Imaging Archive as the external test set. Using the arterial phase and T2WI sequences, expert radiologists manually delineated all images. Using deep learning, liver tumors and liver segments were automatically segmented. A preliminary liver segmentation was performed using the UNet + + network, and the segmented liver mask was re-input as the input end into the UNet + + network to segment liver tumors. The false positivity rate was reduced using a threshold value in the liver tumor segmentation. To evaluate the segmentation results, we calculated the Dice similarity coefficient (DSC), average false positivity rate (AFPR), and delineation time. RESULTS: The average DSC of the liver in the validation and internal testing sets was 0.91 and 0.92, respectively. In the validation set, manual and automatic delineation took 182.9 and 2.2 s, respectively. On an average, manual and automatic delineation took 169.8 and 1.7 s, respectively. The average DSC of liver tumors was 0.612 and 0.687 in the validation and internal testing sets, respectively. The average time for manual and automatic delineation and AFPR in the internal testing set were 47.4 s, 2.9 s, and 1.4, respectively, and those in the external test set were 29.5 s, 4.2 s, and 1.6, respectively. CONCLUSION: UNet + + can automatically segment normal hepatic tissue and liver tumors based on MR images. It provides a methodological basis for the automated segmentation of liver tumors, improves the delineation efficiency, and meets the requirement of extraction set analysis of further radiomics and deep learning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11432-x. BioMed Central 2023-11-03 /pmc/articles/PMC10623778/ /pubmed/37923988 http://dx.doi.org/10.1186/s12885-023-11432-x Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wang, Jing Peng, Yanyang Jing, Shi Han, Lujun Li, Tian Luo, Junpeng A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++ |
title | A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++ |
title_full | A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++ |
title_fullStr | A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++ |
title_full_unstemmed | A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++ |
title_short | A deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using UNet++ |
title_sort | deep-learning approach for segmentation of liver tumors in magnetic resonance imaging using unet++ |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623778/ https://www.ncbi.nlm.nih.gov/pubmed/37923988 http://dx.doi.org/10.1186/s12885-023-11432-x |
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