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Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders
Objective and Impact Statement. We adopt a deep learning model for bone osteolysis prediction on computed tomography (CT) images of murine breast cancer bone metastases. Given the bone CT scans at previous time steps, the model incorporates the bone-cancer interactions learned from the sequential im...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AAAS
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521666/ https://www.ncbi.nlm.nih.gov/pubmed/37850158 http://dx.doi.org/10.34133/2022/9763284 |
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author | Xiong, Wei Yeung, Neil Wang, Shubo Liao, Haofu Wang, Liyun Luo, Jiebo |
author_facet | Xiong, Wei Yeung, Neil Wang, Shubo Liao, Haofu Wang, Liyun Luo, Jiebo |
author_sort | Xiong, Wei |
collection | PubMed |
description | Objective and Impact Statement. We adopt a deep learning model for bone osteolysis prediction on computed tomography (CT) images of murine breast cancer bone metastases. Given the bone CT scans at previous time steps, the model incorporates the bone-cancer interactions learned from the sequential images and generates future CT images. Its ability of predicting the development of bone lesions in cancer-invading bones can assist in assessing the risk of impending fractures and choosing proper treatments in breast cancer bone metastasis. Introduction. Breast cancer often metastasizes to bone, causes osteolytic lesions, and results in skeletal-related events (SREs) including severe pain and even fatal fractures. Although current imaging techniques can detect macroscopic bone lesions, predicting the occurrence and progression of bone lesions remains a challenge. Methods. We adopt a temporal variational autoencoder (T-VAE) model that utilizes a combination of variational autoencoders and long short-term memory networks to predict bone lesion emergence on our micro-CT dataset containing sequential images of murine tibiae. Given the CT scans of murine tibiae at early weeks, our model can learn the distribution of their future states from data. Results. We test our model against other deep learning-based prediction models on the bone lesion progression prediction task. Our model produces much more accurate predictions than existing models under various evaluation metrics. Conclusion. We develop a deep learning framework that can accurately predict and visualize the progression of osteolytic bone lesions. It will assist in planning and evaluating treatment strategies to prevent SREs in breast cancer patients. |
format | Online Article Text |
id | pubmed-10521666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AAAS |
record_format | MEDLINE/PubMed |
spelling | pubmed-105216662023-10-17 Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders Xiong, Wei Yeung, Neil Wang, Shubo Liao, Haofu Wang, Liyun Luo, Jiebo BME Front Research Article Objective and Impact Statement. We adopt a deep learning model for bone osteolysis prediction on computed tomography (CT) images of murine breast cancer bone metastases. Given the bone CT scans at previous time steps, the model incorporates the bone-cancer interactions learned from the sequential images and generates future CT images. Its ability of predicting the development of bone lesions in cancer-invading bones can assist in assessing the risk of impending fractures and choosing proper treatments in breast cancer bone metastasis. Introduction. Breast cancer often metastasizes to bone, causes osteolytic lesions, and results in skeletal-related events (SREs) including severe pain and even fatal fractures. Although current imaging techniques can detect macroscopic bone lesions, predicting the occurrence and progression of bone lesions remains a challenge. Methods. We adopt a temporal variational autoencoder (T-VAE) model that utilizes a combination of variational autoencoders and long short-term memory networks to predict bone lesion emergence on our micro-CT dataset containing sequential images of murine tibiae. Given the CT scans of murine tibiae at early weeks, our model can learn the distribution of their future states from data. Results. We test our model against other deep learning-based prediction models on the bone lesion progression prediction task. Our model produces much more accurate predictions than existing models under various evaluation metrics. Conclusion. We develop a deep learning framework that can accurately predict and visualize the progression of osteolytic bone lesions. It will assist in planning and evaluating treatment strategies to prevent SREs in breast cancer patients. AAAS 2022-04-02 /pmc/articles/PMC10521666/ /pubmed/37850158 http://dx.doi.org/10.34133/2022/9763284 Text en Copyright © 2022 Wei Xiong et al. https://creativecommons.org/licenses/by/4.0/Exclusive Licensee Suzhou Institute of Biomedical Engineering and Technology, CAS. Distributed under a Creative Commons Attribution License (CC BY 4.0). (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Research Article Xiong, Wei Yeung, Neil Wang, Shubo Liao, Haofu Wang, Liyun Luo, Jiebo Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders |
title | Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders |
title_full | Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders |
title_fullStr | Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders |
title_full_unstemmed | Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders |
title_short | Breast Cancer Induced Bone Osteolysis Prediction Using Temporal Variational Autoencoders |
title_sort | breast cancer induced bone osteolysis prediction using temporal variational autoencoders |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521666/ https://www.ncbi.nlm.nih.gov/pubmed/37850158 http://dx.doi.org/10.34133/2022/9763284 |
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