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Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer

BACKGROUND: Estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) and Ki67 are the most useful immunohistochemical biomarkers of invasive breast cancer. The purpose of this study is to investigate the possibility of quantitative parameters derived from d...

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Autores principales: Wang, Xiaoxia, Liu, Daihong, Zeng, Xiangfei, Jiang, Shixi, Li, Lan, Yu, Tao, Zhang, Jiuquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791709/
https://www.ncbi.nlm.nih.gov/pubmed/33413654
http://dx.doi.org/10.1186/s40644-020-00370-7
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author Wang, Xiaoxia
Liu, Daihong
Zeng, Xiangfei
Jiang, Shixi
Li, Lan
Yu, Tao
Zhang, Jiuquan
author_facet Wang, Xiaoxia
Liu, Daihong
Zeng, Xiangfei
Jiang, Shixi
Li, Lan
Yu, Tao
Zhang, Jiuquan
author_sort Wang, Xiaoxia
collection PubMed
description BACKGROUND: Estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) and Ki67 are the most useful immunohistochemical biomarkers of invasive breast cancer. The purpose of this study is to investigate the possibility of quantitative parameters derived from dual-energy CT (DECT) to discriminate immunohistochemical biomarkers of invasive breast cancer. METHODS: This prospective study enrolled 120 patients with invasive breast cancer who underwent preoperative contrast-enhanced DECT for staging purposes from June 2019 to January 2020. DECT quantitative parameters, including normalized iodine concentration (NIC), the slope of the spectral Hounsfield unit curve (λ(Hu)), and the normalized effective atomic number (nZ(eff)), were obtained from reconstructed images. DECT quantitative parameters were compared with the expression status, and the correlations with the value of immunohistochemical biomarkers were evaluated. Inter-observer reproducibility analysis was performed to assess the measurement reproducibility of quantitative parameters. The diagnostic performance of the quantitative parameters was analyzed by receiver operating characteristic curve. RESULTS: The ER-negative group tended to display higher venous phase NIC and nZ(eff) compared with the ER-positive group (individually, p = 0.003, 0.011; area under the curve [AUC] of 0.65, 0.60). The PR-negative group demonstrated higher arterial and venous phase NIC compared with the PR-positive group (individually, p = 0.022, 0.005; AUC of 0.63, 0.65). NIC was correlated negatively with the value of ER and PR expression (r = − 0.175 ~ − 0.265, p = 0.002 ~ 0.042). The HER2-positive group tended to display higher venous phase nZ(eff) than the HER2-negative group (p = 0.022; AUC of 0.59). The Ki67 high-proliferation group demonstrated higher arterial phase, venous phase NIC and nZ(eff) than the Ki67 low-proliferation group (p < 0.001 ~ 0.005; AUC of 0.67 ~ 0.75). Both the NIC and nZ(eff) were correlated positively with the value of Ki67 (r = 0.240 ~ 0.490, p < 0.001 ~ 0.014). CONCLUSIONS: NIC and nZ(eff) derived from DECT could be used to discriminate expression status and may associate with the value of immunohistochemical biomarkers of invasive breast cancer.
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spelling pubmed-77917092021-01-11 Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer Wang, Xiaoxia Liu, Daihong Zeng, Xiangfei Jiang, Shixi Li, Lan Yu, Tao Zhang, Jiuquan Cancer Imaging Research Article BACKGROUND: Estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) and Ki67 are the most useful immunohistochemical biomarkers of invasive breast cancer. The purpose of this study is to investigate the possibility of quantitative parameters derived from dual-energy CT (DECT) to discriminate immunohistochemical biomarkers of invasive breast cancer. METHODS: This prospective study enrolled 120 patients with invasive breast cancer who underwent preoperative contrast-enhanced DECT for staging purposes from June 2019 to January 2020. DECT quantitative parameters, including normalized iodine concentration (NIC), the slope of the spectral Hounsfield unit curve (λ(Hu)), and the normalized effective atomic number (nZ(eff)), were obtained from reconstructed images. DECT quantitative parameters were compared with the expression status, and the correlations with the value of immunohistochemical biomarkers were evaluated. Inter-observer reproducibility analysis was performed to assess the measurement reproducibility of quantitative parameters. The diagnostic performance of the quantitative parameters was analyzed by receiver operating characteristic curve. RESULTS: The ER-negative group tended to display higher venous phase NIC and nZ(eff) compared with the ER-positive group (individually, p = 0.003, 0.011; area under the curve [AUC] of 0.65, 0.60). The PR-negative group demonstrated higher arterial and venous phase NIC compared with the PR-positive group (individually, p = 0.022, 0.005; AUC of 0.63, 0.65). NIC was correlated negatively with the value of ER and PR expression (r = − 0.175 ~ − 0.265, p = 0.002 ~ 0.042). The HER2-positive group tended to display higher venous phase nZ(eff) than the HER2-negative group (p = 0.022; AUC of 0.59). The Ki67 high-proliferation group demonstrated higher arterial phase, venous phase NIC and nZ(eff) than the Ki67 low-proliferation group (p < 0.001 ~ 0.005; AUC of 0.67 ~ 0.75). Both the NIC and nZ(eff) were correlated positively with the value of Ki67 (r = 0.240 ~ 0.490, p < 0.001 ~ 0.014). CONCLUSIONS: NIC and nZ(eff) derived from DECT could be used to discriminate expression status and may associate with the value of immunohistochemical biomarkers of invasive breast cancer. BioMed Central 2021-01-07 /pmc/articles/PMC7791709/ /pubmed/33413654 http://dx.doi.org/10.1186/s40644-020-00370-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Wang, Xiaoxia
Liu, Daihong
Zeng, Xiangfei
Jiang, Shixi
Li, Lan
Yu, Tao
Zhang, Jiuquan
Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer
title Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer
title_full Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer
title_fullStr Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer
title_full_unstemmed Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer
title_short Dual-energy CT quantitative parameters for evaluating Immunohistochemical biomarkers of invasive breast cancer
title_sort dual-energy ct quantitative parameters for evaluating immunohistochemical biomarkers of invasive breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791709/
https://www.ncbi.nlm.nih.gov/pubmed/33413654
http://dx.doi.org/10.1186/s40644-020-00370-7
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