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Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis
Molecular-based subclassifications of breast cancer are important for identifying treatment options and stratifying the prognosis in breast cancer. This study aimed to assess the prognosis relative to disease-free survival (DFS) and overall survival (OS) in patients with triple-negative breast cance...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9914743/ https://www.ncbi.nlm.nih.gov/pubmed/36766486 http://dx.doi.org/10.3390/diagnostics13030372 |
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author | Schulmeyer, Carla E. Fasching, Peter A. Häberle, Lothar Meyer, Julia Schneider, Michael Wachter, David Ruebner, Matthias Pöschke, Patrik Beckmann, Matthias W. Hartmann, Arndt Erber, Ramona Gass, Paul |
author_facet | Schulmeyer, Carla E. Fasching, Peter A. Häberle, Lothar Meyer, Julia Schneider, Michael Wachter, David Ruebner, Matthias Pöschke, Patrik Beckmann, Matthias W. Hartmann, Arndt Erber, Ramona Gass, Paul |
author_sort | Schulmeyer, Carla E. |
collection | PubMed |
description | Molecular-based subclassifications of breast cancer are important for identifying treatment options and stratifying the prognosis in breast cancer. This study aimed to assess the prognosis relative to disease-free survival (DFS) and overall survival (OS) in patients with triple-negative breast cancer (TNBC) and other subtypes, using a biomarker panel including cytokeratin 5 (CK5), cluster of differentiation 117 (CD117), and epidermal growth factor receptor (EGFR). This cohort–case study included histologically confirmed breast carcinomas as cohort arm. From a total of 894 patients, 572 patients with early breast cancer, sufficient clinical data, and archived tumor tissue were included. Using the immunohistochemical markers CK5, CD117, and EGFR, two subgroups were formed: one with all three biomarkers negative (TBN) and one with at least one of those three biomarkers positive (non-TBN). There were significant differences between the two biomarker subgroups (TBN versus non-TBN) in TNBC for DFS (p = 0.04) and OS (p = 0.02), with higher survival rates (DFS and OS) in the non-TBN subgroup. In this study, we found the non-TBN subgroup of TNBC lesions with at least one positive biomarker of CK5, CD117, and/or EGFR, to be associated with longer DFS and OS. |
format | Online Article Text |
id | pubmed-9914743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99147432023-02-11 Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis Schulmeyer, Carla E. Fasching, Peter A. Häberle, Lothar Meyer, Julia Schneider, Michael Wachter, David Ruebner, Matthias Pöschke, Patrik Beckmann, Matthias W. Hartmann, Arndt Erber, Ramona Gass, Paul Diagnostics (Basel) Article Molecular-based subclassifications of breast cancer are important for identifying treatment options and stratifying the prognosis in breast cancer. This study aimed to assess the prognosis relative to disease-free survival (DFS) and overall survival (OS) in patients with triple-negative breast cancer (TNBC) and other subtypes, using a biomarker panel including cytokeratin 5 (CK5), cluster of differentiation 117 (CD117), and epidermal growth factor receptor (EGFR). This cohort–case study included histologically confirmed breast carcinomas as cohort arm. From a total of 894 patients, 572 patients with early breast cancer, sufficient clinical data, and archived tumor tissue were included. Using the immunohistochemical markers CK5, CD117, and EGFR, two subgroups were formed: one with all three biomarkers negative (TBN) and one with at least one of those three biomarkers positive (non-TBN). There were significant differences between the two biomarker subgroups (TBN versus non-TBN) in TNBC for DFS (p = 0.04) and OS (p = 0.02), with higher survival rates (DFS and OS) in the non-TBN subgroup. In this study, we found the non-TBN subgroup of TNBC lesions with at least one positive biomarker of CK5, CD117, and/or EGFR, to be associated with longer DFS and OS. MDPI 2023-01-19 /pmc/articles/PMC9914743/ /pubmed/36766486 http://dx.doi.org/10.3390/diagnostics13030372 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Schulmeyer, Carla E. Fasching, Peter A. Häberle, Lothar Meyer, Julia Schneider, Michael Wachter, David Ruebner, Matthias Pöschke, Patrik Beckmann, Matthias W. Hartmann, Arndt Erber, Ramona Gass, Paul Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis |
title | Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis |
title_full | Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis |
title_fullStr | Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis |
title_full_unstemmed | Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis |
title_short | Expression of the Immunohistochemical Markers CK5, CD117, and EGFR in Molecular Subtypes of Breast Cancer Correlated with Prognosis |
title_sort | expression of the immunohistochemical markers ck5, cd117, and egfr in molecular subtypes of breast cancer correlated with prognosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9914743/ https://www.ncbi.nlm.nih.gov/pubmed/36766486 http://dx.doi.org/10.3390/diagnostics13030372 |
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