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Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study
OBJECTIVE: To develop and validate a deep learning (DL) model based on CT for differentiating bone islands and osteoblastic bone metastases. MATERIALS AND METHODS: The patients with sclerosing bone lesions (SBLs) were retrospectively included in three hospitals. The images from site 1 were randomly...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415522/ https://www.ncbi.nlm.nih.gov/pubmed/37060446 http://dx.doi.org/10.1007/s00330-023-09573-5 |
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author | Xiong, Yuchao Guo, Wei Liang, Zhiping Wu, Li Ye, Guoxi Liang, Ying-ying Wen, Chao Yang, Feng Chen, Song Zeng, Xu-wen Xu, Fan |
author_facet | Xiong, Yuchao Guo, Wei Liang, Zhiping Wu, Li Ye, Guoxi Liang, Ying-ying Wen, Chao Yang, Feng Chen, Song Zeng, Xu-wen Xu, Fan |
author_sort | Xiong, Yuchao |
collection | PubMed |
description | OBJECTIVE: To develop and validate a deep learning (DL) model based on CT for differentiating bone islands and osteoblastic bone metastases. MATERIALS AND METHODS: The patients with sclerosing bone lesions (SBLs) were retrospectively included in three hospitals. The images from site 1 were randomly assigned to the training (70%) and intrinsic verification (10%) datasets for developing the two-dimensional (2D) DL model (single-slice input) and “2.5-dimensional” (2.5D) DL model (three-slice input) and to the internal validation dataset (20%) for evaluating the performance of both models. The diagnostic performance was evaluated using the internal validation set from site 1 and additional external validation datasets from site 2 and site 3. And statistically analyze the performance of 2D and 2.5D DL models. RESULTS: In total, 1918 SBLs in 728 patients in site 1, 122 SBLs in 71 patients in site 2, and 71 SBLs in 47 patients in site 3 were used to develop and test the 2D and 2.5D DL models. The best performance was obtained using the 2.5D DL model, which achieved an AUC of 0.996 (95% confidence interval [CI], 0.995–0.996), 0.958 (95% CI, 0.958–0.960), and 0.952 (95% CI, 0.951–0.953) and accuracies of 0.950, 0.902, and 0.863 for the internal validation set, the external validation set from site 2 and site 3, respectively. CONCLUSION: A DL model based on a three-slice CT image input (2.5D DL model) can improve the prediction of osteoblastic bone metastases, which can facilitate clinical decision-making. KEY POINTS: • This study investigated the value of deep learning models in identifying bone islands and osteoblastic bone metastases. • Three-slice CT image input (2.5D DL model) outweighed the 2D model in the classification of sclerosing bone lesions. • The 2.5D deep learning model showed excellent performance using the internal (AUC, 0.996) and two external (AUC, 0.958; AUC, 0.952) validation sets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00330-023-09573-5. |
format | Online Article Text |
id | pubmed-10415522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-104155222023-08-12 Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study Xiong, Yuchao Guo, Wei Liang, Zhiping Wu, Li Ye, Guoxi Liang, Ying-ying Wen, Chao Yang, Feng Chen, Song Zeng, Xu-wen Xu, Fan Eur Radiol Musculoskeletal OBJECTIVE: To develop and validate a deep learning (DL) model based on CT for differentiating bone islands and osteoblastic bone metastases. MATERIALS AND METHODS: The patients with sclerosing bone lesions (SBLs) were retrospectively included in three hospitals. The images from site 1 were randomly assigned to the training (70%) and intrinsic verification (10%) datasets for developing the two-dimensional (2D) DL model (single-slice input) and “2.5-dimensional” (2.5D) DL model (three-slice input) and to the internal validation dataset (20%) for evaluating the performance of both models. The diagnostic performance was evaluated using the internal validation set from site 1 and additional external validation datasets from site 2 and site 3. And statistically analyze the performance of 2D and 2.5D DL models. RESULTS: In total, 1918 SBLs in 728 patients in site 1, 122 SBLs in 71 patients in site 2, and 71 SBLs in 47 patients in site 3 were used to develop and test the 2D and 2.5D DL models. The best performance was obtained using the 2.5D DL model, which achieved an AUC of 0.996 (95% confidence interval [CI], 0.995–0.996), 0.958 (95% CI, 0.958–0.960), and 0.952 (95% CI, 0.951–0.953) and accuracies of 0.950, 0.902, and 0.863 for the internal validation set, the external validation set from site 2 and site 3, respectively. CONCLUSION: A DL model based on a three-slice CT image input (2.5D DL model) can improve the prediction of osteoblastic bone metastases, which can facilitate clinical decision-making. KEY POINTS: • This study investigated the value of deep learning models in identifying bone islands and osteoblastic bone metastases. • Three-slice CT image input (2.5D DL model) outweighed the 2D model in the classification of sclerosing bone lesions. • The 2.5D deep learning model showed excellent performance using the internal (AUC, 0.996) and two external (AUC, 0.958; AUC, 0.952) validation sets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00330-023-09573-5. Springer Berlin Heidelberg 2023-04-15 2023 /pmc/articles/PMC10415522/ /pubmed/37060446 http://dx.doi.org/10.1007/s00330-023-09573-5 Text en © The Author(s) 2023 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 | Musculoskeletal Xiong, Yuchao Guo, Wei Liang, Zhiping Wu, Li Ye, Guoxi Liang, Ying-ying Wen, Chao Yang, Feng Chen, Song Zeng, Xu-wen Xu, Fan Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study |
title | Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study |
title_full | Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study |
title_fullStr | Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study |
title_full_unstemmed | Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study |
title_short | Deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study |
title_sort | deep learning–based diagnosis of osteoblastic bone metastases and bone islands in computed tomograph images: a multicenter diagnostic study |
topic | Musculoskeletal |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415522/ https://www.ncbi.nlm.nih.gov/pubmed/37060446 http://dx.doi.org/10.1007/s00330-023-09573-5 |
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