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Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis

Angiogenesis is a critical component of breast cancer development, and identification of imaging-based angiogenesis assays has prognostic and treatment implications. We evaluated the association of semi-quantitative kinetic and radiomic breast cancer features on dynamic contrast-enhanced (DCE)-MRI w...

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Autores principales: Xiao, Jennifer, Rahbar, Habib, Hippe, Daniel S., Rendi, Mara H., Parker, Elizabeth U., Shekar, Neal, Hirano, Michael, Cheung, Kevin J., Partridge, Savannah C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052427/
https://www.ncbi.nlm.nih.gov/pubmed/33863924
http://dx.doi.org/10.1038/s41523-021-00247-3
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author Xiao, Jennifer
Rahbar, Habib
Hippe, Daniel S.
Rendi, Mara H.
Parker, Elizabeth U.
Shekar, Neal
Hirano, Michael
Cheung, Kevin J.
Partridge, Savannah C.
author_facet Xiao, Jennifer
Rahbar, Habib
Hippe, Daniel S.
Rendi, Mara H.
Parker, Elizabeth U.
Shekar, Neal
Hirano, Michael
Cheung, Kevin J.
Partridge, Savannah C.
author_sort Xiao, Jennifer
collection PubMed
description Angiogenesis is a critical component of breast cancer development, and identification of imaging-based angiogenesis assays has prognostic and treatment implications. We evaluated the association of semi-quantitative kinetic and radiomic breast cancer features on dynamic contrast-enhanced (DCE)-MRI with microvessel density (MVD), a marker for angiogenesis. Invasive breast cancer kinetic features (initial peak percent enhancement [PE], signal enhancement ratio [SER], functional tumor volume [FTV], and washout fraction [WF]), radiomics features (108 total features reflecting tumor morphology, signal intensity, and texture), and MVD (by histologic CD31 immunostaining) were measured in 27 patients (1/2016–7/2017). Lesions with high MVD levels demonstrated higher peak SER than lesions with low MVD (mean: 1.94 vs. 1.61, area under the receiver operating characteristic curve [AUC] = 0.79, p = 0.009) and higher WF (mean: 50.6% vs. 22.5%, AUC = 0.87, p = 0.001). Several radiomics texture features were also promising for predicting increased MVD (maximum AUC = 0.84, p = 0.002). Our study suggests DCE-MRI can non-invasively assess breast cancer angiogenesis, which could stratify biology and optimize treatments.
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spelling pubmed-80524272021-05-05 Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis Xiao, Jennifer Rahbar, Habib Hippe, Daniel S. Rendi, Mara H. Parker, Elizabeth U. Shekar, Neal Hirano, Michael Cheung, Kevin J. Partridge, Savannah C. NPJ Breast Cancer Article Angiogenesis is a critical component of breast cancer development, and identification of imaging-based angiogenesis assays has prognostic and treatment implications. We evaluated the association of semi-quantitative kinetic and radiomic breast cancer features on dynamic contrast-enhanced (DCE)-MRI with microvessel density (MVD), a marker for angiogenesis. Invasive breast cancer kinetic features (initial peak percent enhancement [PE], signal enhancement ratio [SER], functional tumor volume [FTV], and washout fraction [WF]), radiomics features (108 total features reflecting tumor morphology, signal intensity, and texture), and MVD (by histologic CD31 immunostaining) were measured in 27 patients (1/2016–7/2017). Lesions with high MVD levels demonstrated higher peak SER than lesions with low MVD (mean: 1.94 vs. 1.61, area under the receiver operating characteristic curve [AUC] = 0.79, p = 0.009) and higher WF (mean: 50.6% vs. 22.5%, AUC = 0.87, p = 0.001). Several radiomics texture features were also promising for predicting increased MVD (maximum AUC = 0.84, p = 0.002). Our study suggests DCE-MRI can non-invasively assess breast cancer angiogenesis, which could stratify biology and optimize treatments. Nature Publishing Group UK 2021-04-16 /pmc/articles/PMC8052427/ /pubmed/33863924 http://dx.doi.org/10.1038/s41523-021-00247-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xiao, Jennifer
Rahbar, Habib
Hippe, Daniel S.
Rendi, Mara H.
Parker, Elizabeth U.
Shekar, Neal
Hirano, Michael
Cheung, Kevin J.
Partridge, Savannah C.
Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis
title Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis
title_full Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis
title_fullStr Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis
title_full_unstemmed Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis
title_short Dynamic contrast-enhanced breast MRI features correlate with invasive breast cancer angiogenesis
title_sort dynamic contrast-enhanced breast mri features correlate with invasive breast cancer angiogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052427/
https://www.ncbi.nlm.nih.gov/pubmed/33863924
http://dx.doi.org/10.1038/s41523-021-00247-3
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