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Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer

BACKGROUND: The goal of this study was to develop and validate a radiomics signature based on dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) preoperatively differentiating luminal and non-luminal molecular subtypes in patients with invasive breast cancer. METHODS: One hundred and thi...

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Autores principales: Huang, Ting, Fan, Bing, Qiu, Yingying, Zhang, Rui, Wang, Xiaolian, Wang, Chaoxiong, Lin, Huashan, Yan, Ting, Dong, Wentao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166881/
https://www.ncbi.nlm.nih.gov/pubmed/37181350
http://dx.doi.org/10.3389/fmed.2023.1140514
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author Huang, Ting
Fan, Bing
Qiu, Yingying
Zhang, Rui
Wang, Xiaolian
Wang, Chaoxiong
Lin, Huashan
Yan, Ting
Dong, Wentao
author_facet Huang, Ting
Fan, Bing
Qiu, Yingying
Zhang, Rui
Wang, Xiaolian
Wang, Chaoxiong
Lin, Huashan
Yan, Ting
Dong, Wentao
author_sort Huang, Ting
collection PubMed
description BACKGROUND: The goal of this study was to develop and validate a radiomics signature based on dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) preoperatively differentiating luminal and non-luminal molecular subtypes in patients with invasive breast cancer. METHODS: One hundred and thirty-five invasive breast cancer patients with luminal (n = 78) and non-luminal (n = 57) molecular subtypes were divided into training set (n = 95) and testing set (n = 40) in a 7:3 ratio. Demographics and MRI radiological features were used to construct clinical risk factors. Radiomics signature was constructed by extracting radiomics features from the second phase of DCE-MRI images and radiomics score (rad-score) was calculated. Finally, the prediction performance was evaluated in terms of calibration, discrimination, and clinical usefulness. RESULTS: Multivariate logistic regression analysis showed that no clinical risk factors were independent predictors of luminal and non-luminal molecular subtypes in invasive breast cancer patients. Meanwhile, the radiomics signature showed good discrimination in the training set (AUC, 0.86; 95% CI, 0.78–0.93) and the testing set (AUC, 0.80; 95% CI, 0.65–0.95). CONCLUSION: The DCE-MRI radiomics signature is a promising tool to discrimination luminal and non-luminal molecular subtypes in invasive breast cancer patients preoperatively and noninvasively.
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spelling pubmed-101668812023-05-10 Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer Huang, Ting Fan, Bing Qiu, Yingying Zhang, Rui Wang, Xiaolian Wang, Chaoxiong Lin, Huashan Yan, Ting Dong, Wentao Front Med (Lausanne) Medicine BACKGROUND: The goal of this study was to develop and validate a radiomics signature based on dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) preoperatively differentiating luminal and non-luminal molecular subtypes in patients with invasive breast cancer. METHODS: One hundred and thirty-five invasive breast cancer patients with luminal (n = 78) and non-luminal (n = 57) molecular subtypes were divided into training set (n = 95) and testing set (n = 40) in a 7:3 ratio. Demographics and MRI radiological features were used to construct clinical risk factors. Radiomics signature was constructed by extracting radiomics features from the second phase of DCE-MRI images and radiomics score (rad-score) was calculated. Finally, the prediction performance was evaluated in terms of calibration, discrimination, and clinical usefulness. RESULTS: Multivariate logistic regression analysis showed that no clinical risk factors were independent predictors of luminal and non-luminal molecular subtypes in invasive breast cancer patients. Meanwhile, the radiomics signature showed good discrimination in the training set (AUC, 0.86; 95% CI, 0.78–0.93) and the testing set (AUC, 0.80; 95% CI, 0.65–0.95). CONCLUSION: The DCE-MRI radiomics signature is a promising tool to discrimination luminal and non-luminal molecular subtypes in invasive breast cancer patients preoperatively and noninvasively. Frontiers Media S.A. 2023-04-25 /pmc/articles/PMC10166881/ /pubmed/37181350 http://dx.doi.org/10.3389/fmed.2023.1140514 Text en Copyright © 2023 Huang, Fan, Qiu, Zhang, Wang, Wang, Lin, Yan and Dong. 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 Medicine
Huang, Ting
Fan, Bing
Qiu, Yingying
Zhang, Rui
Wang, Xiaolian
Wang, Chaoxiong
Lin, Huashan
Yan, Ting
Dong, Wentao
Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer
title Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer
title_full Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer
title_fullStr Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer
title_full_unstemmed Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer
title_short Application of DCE-MRI radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer
title_sort application of dce-mri radiomics signature analysis in differentiating molecular subtypes of luminal and non-luminal breast cancer
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166881/
https://www.ncbi.nlm.nih.gov/pubmed/37181350
http://dx.doi.org/10.3389/fmed.2023.1140514
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