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Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss

PURPOSE: To establish a high-risk prediction model for aromatase inhibitor-associated bone loss (AIBL) in patients with hormone receptor-positive breast cancer. METHODS: The study included breast cancer patients who received aromatase inhibitor (AI) treatment. Univariate analysis was performed to id...

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Autores principales: Chu, Meiling, Zhou, Yue, Yin, Yulian, Jin, Lan, Chen, Hongfeng, Meng, Tian, He, Binjun, Wu, Jingjing, Ye, Meina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174287/
https://www.ncbi.nlm.nih.gov/pubmed/37182163
http://dx.doi.org/10.3389/fonc.2023.1182792
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author Chu, Meiling
Zhou, Yue
Yin, Yulian
Jin, Lan
Chen, Hongfeng
Meng, Tian
He, Binjun
Wu, Jingjing
Ye, Meina
author_facet Chu, Meiling
Zhou, Yue
Yin, Yulian
Jin, Lan
Chen, Hongfeng
Meng, Tian
He, Binjun
Wu, Jingjing
Ye, Meina
author_sort Chu, Meiling
collection PubMed
description PURPOSE: To establish a high-risk prediction model for aromatase inhibitor-associated bone loss (AIBL) in patients with hormone receptor-positive breast cancer. METHODS: The study included breast cancer patients who received aromatase inhibitor (AI) treatment. Univariate analysis was performed to identify risk factors associated with AIBL. The dataset was randomly divided into a training set (70%) and a test set (30%). The identified risk factors were used to construct a prediction model using the eXtreme gradient boosting (XGBoost) machine learning method. Logistic regression and least absolute shrinkage and selection operator (LASSO) regression methods were used for comparison. The area under the receiver operating characteristic curve (AUC) was used to evaluate the performance of the model in the test dataset. RESULTS: A total of 113 subjects were included in the study. Duration of breast cancer, duration of aromatase inhibitor therapy, hip fracture index, major osteoporotic fracture index, prolactin (PRL), and osteocalcin (OC) were found to be independent risk factors for AIBL (p < 0.05). The XGBoost model had a higher AUC compared to the logistic model and LASSO model (0.761 vs. 0.716, 0.691). CONCLUSION: The XGBoost model outperformed the logistic and LASSO models in predicting the occurrence of AIBL in patients with hormone receptor-positive breast cancer receiving aromatase inhibitors.
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spelling pubmed-101742872023-05-12 Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss Chu, Meiling Zhou, Yue Yin, Yulian Jin, Lan Chen, Hongfeng Meng, Tian He, Binjun Wu, Jingjing Ye, Meina Front Oncol Oncology PURPOSE: To establish a high-risk prediction model for aromatase inhibitor-associated bone loss (AIBL) in patients with hormone receptor-positive breast cancer. METHODS: The study included breast cancer patients who received aromatase inhibitor (AI) treatment. Univariate analysis was performed to identify risk factors associated with AIBL. The dataset was randomly divided into a training set (70%) and a test set (30%). The identified risk factors were used to construct a prediction model using the eXtreme gradient boosting (XGBoost) machine learning method. Logistic regression and least absolute shrinkage and selection operator (LASSO) regression methods were used for comparison. The area under the receiver operating characteristic curve (AUC) was used to evaluate the performance of the model in the test dataset. RESULTS: A total of 113 subjects were included in the study. Duration of breast cancer, duration of aromatase inhibitor therapy, hip fracture index, major osteoporotic fracture index, prolactin (PRL), and osteocalcin (OC) were found to be independent risk factors for AIBL (p < 0.05). The XGBoost model had a higher AUC compared to the logistic model and LASSO model (0.761 vs. 0.716, 0.691). CONCLUSION: The XGBoost model outperformed the logistic and LASSO models in predicting the occurrence of AIBL in patients with hormone receptor-positive breast cancer receiving aromatase inhibitors. Frontiers Media S.A. 2023-04-27 /pmc/articles/PMC10174287/ /pubmed/37182163 http://dx.doi.org/10.3389/fonc.2023.1182792 Text en Copyright © 2023 Chu, Zhou, Yin, Jin, Chen, Meng, He, Wu and Ye 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
Chu, Meiling
Zhou, Yue
Yin, Yulian
Jin, Lan
Chen, Hongfeng
Meng, Tian
He, Binjun
Wu, Jingjing
Ye, Meina
Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss
title Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss
title_full Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss
title_fullStr Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss
title_full_unstemmed Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss
title_short Construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss
title_sort construction and validation of a risk prediction model for aromatase inhibitor-associated bone loss
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174287/
https://www.ncbi.nlm.nih.gov/pubmed/37182163
http://dx.doi.org/10.3389/fonc.2023.1182792
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