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Association between digital breast tomosynthesis and molecular subtypes of breast cancer

In recent years, with increasing prevalence, particularly in young patients, breast cancer is considered to be one of the most common malignancies. The aim of the present study was to evaluate the clinical value of digital breast tomosynthesis (DBT) in diagnosing molecular subtypes of breast cancer....

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Autores principales: Cai, Siqing, Yao, Miaomiao, Cai, Donglu, Yan, Jianxiang, Huang, Meiling, Yan, Lisheng, Huang, Huirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366033/
https://www.ncbi.nlm.nih.gov/pubmed/30867729
http://dx.doi.org/10.3892/ol.2019.9918
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author Cai, Siqing
Yao, Miaomiao
Cai, Donglu
Yan, Jianxiang
Huang, Meiling
Yan, Lisheng
Huang, Huirong
author_facet Cai, Siqing
Yao, Miaomiao
Cai, Donglu
Yan, Jianxiang
Huang, Meiling
Yan, Lisheng
Huang, Huirong
author_sort Cai, Siqing
collection PubMed
description In recent years, with increasing prevalence, particularly in young patients, breast cancer is considered to be one of the most common malignancies. The aim of the present study was to evaluate the clinical value of digital breast tomosynthesis (DBT) in diagnosing molecular subtypes of breast cancer. The present study retrospectively analyzed 134 cases of breast cancer with data regarding surgery, complete pathology and immunohistochemistry, which were collected at The Second Clinical College of Fujian Medical University (Quanzhou, China) between May 2013 and October 2014. The patients were divided into the four following molecular subtypes: Luminal A, luminal B, triple-negative and human epidermal growth factor receptor 2 (HER-2) overexpression, according to the expression of estrogen receptor, progesterone hormone receptor, HER-2 and Ki67. The association between clinical characteristics of each molecular subtype and characteristics of DBT were assessed. Calcification scores and lymph node size were the indicators that exhibited a significant difference following comparison between the four molecular subtypes. The subgroup analysis based on tumor size, calcification scores and lymph node size identified a significant difference in the distribution between patients with breast cancer with lymph node size of ≥1.5 and <1.5 cm. The analysis also revealed that the molecular subtypes of breast cancer were significantly associated with variables of calcification scores and lymph node size. In conclusion, the diagnostic imaging features, including calcification score and lymph node size, determined using DBT could be used as assistant diagnostic markers of breast cancer molecular subtypes.
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spelling pubmed-63660332019-03-13 Association between digital breast tomosynthesis and molecular subtypes of breast cancer Cai, Siqing Yao, Miaomiao Cai, Donglu Yan, Jianxiang Huang, Meiling Yan, Lisheng Huang, Huirong Oncol Lett Articles In recent years, with increasing prevalence, particularly in young patients, breast cancer is considered to be one of the most common malignancies. The aim of the present study was to evaluate the clinical value of digital breast tomosynthesis (DBT) in diagnosing molecular subtypes of breast cancer. The present study retrospectively analyzed 134 cases of breast cancer with data regarding surgery, complete pathology and immunohistochemistry, which were collected at The Second Clinical College of Fujian Medical University (Quanzhou, China) between May 2013 and October 2014. The patients were divided into the four following molecular subtypes: Luminal A, luminal B, triple-negative and human epidermal growth factor receptor 2 (HER-2) overexpression, according to the expression of estrogen receptor, progesterone hormone receptor, HER-2 and Ki67. The association between clinical characteristics of each molecular subtype and characteristics of DBT were assessed. Calcification scores and lymph node size were the indicators that exhibited a significant difference following comparison between the four molecular subtypes. The subgroup analysis based on tumor size, calcification scores and lymph node size identified a significant difference in the distribution between patients with breast cancer with lymph node size of ≥1.5 and <1.5 cm. The analysis also revealed that the molecular subtypes of breast cancer were significantly associated with variables of calcification scores and lymph node size. In conclusion, the diagnostic imaging features, including calcification score and lymph node size, determined using DBT could be used as assistant diagnostic markers of breast cancer molecular subtypes. D.A. Spandidos 2019-03 2019-01-10 /pmc/articles/PMC6366033/ /pubmed/30867729 http://dx.doi.org/10.3892/ol.2019.9918 Text en Copyright: © Cai et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Cai, Siqing
Yao, Miaomiao
Cai, Donglu
Yan, Jianxiang
Huang, Meiling
Yan, Lisheng
Huang, Huirong
Association between digital breast tomosynthesis and molecular subtypes of breast cancer
title Association between digital breast tomosynthesis and molecular subtypes of breast cancer
title_full Association between digital breast tomosynthesis and molecular subtypes of breast cancer
title_fullStr Association between digital breast tomosynthesis and molecular subtypes of breast cancer
title_full_unstemmed Association between digital breast tomosynthesis and molecular subtypes of breast cancer
title_short Association between digital breast tomosynthesis and molecular subtypes of breast cancer
title_sort association between digital breast tomosynthesis and molecular subtypes of breast cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366033/
https://www.ncbi.nlm.nih.gov/pubmed/30867729
http://dx.doi.org/10.3892/ol.2019.9918
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