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Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models

The risk of osteoporosis in breast cancer patients is higher than that in healthy populations. The fracture and death rates increase after patients are diagnosed with osteoporosis. We aimed to develop machine learning-based models to predict the risk of osteoporosis as well as the relative fracture...

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Autores principales: Ji, Lichen, Zhang, Wei, Zhong, Xugang, Zhao, Tingxiao, Sun, Xixi, Zhu, Senbo, Tong, Yu, Luo, Junchao, Xu, Youjia, Yang, Di, Kang, Yao, Wang, Jin, Bi, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417646/
https://www.ncbi.nlm.nih.gov/pubmed/36033513
http://dx.doi.org/10.3389/fonc.2022.973307
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author Ji, Lichen
Zhang, Wei
Zhong, Xugang
Zhao, Tingxiao
Sun, Xixi
Zhu, Senbo
Tong, Yu
Luo, Junchao
Xu, Youjia
Yang, Di
Kang, Yao
Wang, Jin
Bi, Qing
author_facet Ji, Lichen
Zhang, Wei
Zhong, Xugang
Zhao, Tingxiao
Sun, Xixi
Zhu, Senbo
Tong, Yu
Luo, Junchao
Xu, Youjia
Yang, Di
Kang, Yao
Wang, Jin
Bi, Qing
author_sort Ji, Lichen
collection PubMed
description The risk of osteoporosis in breast cancer patients is higher than that in healthy populations. The fracture and death rates increase after patients are diagnosed with osteoporosis. We aimed to develop machine learning-based models to predict the risk of osteoporosis as well as the relative fracture occurrence and prognosis. We selected 749 breast cancer patients from two independent Chinese centers and applied six different methods of machine learning to develop osteoporosis, fracture and survival risk assessment models. The performance of the models was compared with that of current models, such as FRAX, OSTA and TNM, by applying ROC, DCA curve analysis, and the calculation of accuracy and sensitivity in both internal and independent external cohorts. Three models were developed. The XGB model demonstrated the best discriminatory performance among the models. Internal and external validation revealed that the AUCs of the osteoporosis model were 0.86 and 0.87, compared with the FRAX model (0.84 and 0.72)/OSTA model (0.77 and 0.66), respectively. The fracture model had high AUCs in the internal and external cohorts of 0.93 and 0.92, which were higher than those of the FRAX model (0.89 and 0.86). The survival model was also assessed and showed high reliability via internal and external validation (AUC of 0.96 and 0.95), which was better than that of the TNM model (AUCs of 0.87 and 0.87). Our models offer a solid approach to help improve decision making.
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spelling pubmed-94176462022-08-27 Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models Ji, Lichen Zhang, Wei Zhong, Xugang Zhao, Tingxiao Sun, Xixi Zhu, Senbo Tong, Yu Luo, Junchao Xu, Youjia Yang, Di Kang, Yao Wang, Jin Bi, Qing Front Oncol Oncology The risk of osteoporosis in breast cancer patients is higher than that in healthy populations. The fracture and death rates increase after patients are diagnosed with osteoporosis. We aimed to develop machine learning-based models to predict the risk of osteoporosis as well as the relative fracture occurrence and prognosis. We selected 749 breast cancer patients from two independent Chinese centers and applied six different methods of machine learning to develop osteoporosis, fracture and survival risk assessment models. The performance of the models was compared with that of current models, such as FRAX, OSTA and TNM, by applying ROC, DCA curve analysis, and the calculation of accuracy and sensitivity in both internal and independent external cohorts. Three models were developed. The XGB model demonstrated the best discriminatory performance among the models. Internal and external validation revealed that the AUCs of the osteoporosis model were 0.86 and 0.87, compared with the FRAX model (0.84 and 0.72)/OSTA model (0.77 and 0.66), respectively. The fracture model had high AUCs in the internal and external cohorts of 0.93 and 0.92, which were higher than those of the FRAX model (0.89 and 0.86). The survival model was also assessed and showed high reliability via internal and external validation (AUC of 0.96 and 0.95), which was better than that of the TNM model (AUCs of 0.87 and 0.87). Our models offer a solid approach to help improve decision making. Frontiers Media S.A. 2022-08-12 /pmc/articles/PMC9417646/ /pubmed/36033513 http://dx.doi.org/10.3389/fonc.2022.973307 Text en Copyright © 2022 Ji, Zhang, Zhong, Zhao, Sun, Zhu, Tong, Luo, Xu, Yang, Kang, Wang and Bi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Ji, Lichen
Zhang, Wei
Zhong, Xugang
Zhao, Tingxiao
Sun, Xixi
Zhu, Senbo
Tong, Yu
Luo, Junchao
Xu, Youjia
Yang, Di
Kang, Yao
Wang, Jin
Bi, Qing
Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models
title Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models
title_full Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models
title_fullStr Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models
title_full_unstemmed Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models
title_short Osteoporosis, fracture and survival: Application of machine learning in breast cancer prediction models
title_sort osteoporosis, fracture and survival: application of machine learning in breast cancer prediction models
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417646/
https://www.ncbi.nlm.nih.gov/pubmed/36033513
http://dx.doi.org/10.3389/fonc.2022.973307
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