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EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer

PURPOSE: Evaluating consecutive early breast cancer patients, we analyzed both the impact of EndoPredict(®) on clinical decisions as well as clinico-pathological factors influencing the decision to perform this gene expression test. METHODS: Hormone receptor (HR)-positive and human epidermal growth...

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Autores principales: Almstedt, K., Mendoza, S., Otto, M., Battista, M. J., Steetskamp, J., Heimes, A. S., Krajnak, S., Poplawski, A., Gerhold-Ay, A., Hasenburg, A., Denkert, C., Schmidt, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275019/
https://www.ncbi.nlm.nih.gov/pubmed/32436145
http://dx.doi.org/10.1007/s10549-020-05688-1
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author Almstedt, K.
Mendoza, S.
Otto, M.
Battista, M. J.
Steetskamp, J.
Heimes, A. S.
Krajnak, S.
Poplawski, A.
Gerhold-Ay, A.
Hasenburg, A.
Denkert, C.
Schmidt, M.
author_facet Almstedt, K.
Mendoza, S.
Otto, M.
Battista, M. J.
Steetskamp, J.
Heimes, A. S.
Krajnak, S.
Poplawski, A.
Gerhold-Ay, A.
Hasenburg, A.
Denkert, C.
Schmidt, M.
author_sort Almstedt, K.
collection PubMed
description PURPOSE: Evaluating consecutive early breast cancer patients, we analyzed both the impact of EndoPredict(®) on clinical decisions as well as clinico-pathological factors influencing the decision to perform this gene expression test. METHODS: Hormone receptor (HR)-positive and human epidermal growth factor receptor 2 (HER2)-negative early breast cancer patients treated between 2011 and 2016 were included in this study to investigate the role of EndoPredict(®) (EPclin) in the treatment of early breast cancer. A main study aim was to analyze the changes in therapy recommendations with and without EPclin. In addition, the impact of clinico-pathological parameters for the decision to perform EPclin was examined by Pearson's chi-squared test (χ(2)-test) and Fisher's exact test as well as univariate and multivariate logistic regressions. RESULTS: In a cohort of 869 consecutive early HR-positive, HER-negative breast cancer patients, EPclin was utilized in 156 (18.0%) patients. EPclin led to changes in therapy recommendations in 33.3% (n = 52), with both therapy escalation in 19.2% (n = 30) and de-escalation in 14.1% (n = 22). The clinico-pathological factors influencing the use of EPclin were age (P < 0.001, odds ratio [OR] 0.498), tumor size (P = 0.011, OR 0.071), nodal status (P = 0.021, OR 1.674), histological grade (P = 0.043, OR 0.432), and Ki-67 (P < 0.001, OR 3.599). CONCLUSIONS: EPclin led to a change in therapy recommendations in one third of the patients. Clinico-pathological parameters such as younger age, smaller tumor size, positive nodal status, intermediate histological grade and intermediate Ki-67 had a significant influence on the use of EndoPredict(®). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10549-020-05688-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-72750192020-06-16 EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer Almstedt, K. Mendoza, S. Otto, M. Battista, M. J. Steetskamp, J. Heimes, A. S. Krajnak, S. Poplawski, A. Gerhold-Ay, A. Hasenburg, A. Denkert, C. Schmidt, M. Breast Cancer Res Treat Clinical Trial PURPOSE: Evaluating consecutive early breast cancer patients, we analyzed both the impact of EndoPredict(®) on clinical decisions as well as clinico-pathological factors influencing the decision to perform this gene expression test. METHODS: Hormone receptor (HR)-positive and human epidermal growth factor receptor 2 (HER2)-negative early breast cancer patients treated between 2011 and 2016 were included in this study to investigate the role of EndoPredict(®) (EPclin) in the treatment of early breast cancer. A main study aim was to analyze the changes in therapy recommendations with and without EPclin. In addition, the impact of clinico-pathological parameters for the decision to perform EPclin was examined by Pearson's chi-squared test (χ(2)-test) and Fisher's exact test as well as univariate and multivariate logistic regressions. RESULTS: In a cohort of 869 consecutive early HR-positive, HER-negative breast cancer patients, EPclin was utilized in 156 (18.0%) patients. EPclin led to changes in therapy recommendations in 33.3% (n = 52), with both therapy escalation in 19.2% (n = 30) and de-escalation in 14.1% (n = 22). The clinico-pathological factors influencing the use of EPclin were age (P < 0.001, odds ratio [OR] 0.498), tumor size (P = 0.011, OR 0.071), nodal status (P = 0.021, OR 1.674), histological grade (P = 0.043, OR 0.432), and Ki-67 (P < 0.001, OR 3.599). CONCLUSIONS: EPclin led to a change in therapy recommendations in one third of the patients. Clinico-pathological parameters such as younger age, smaller tumor size, positive nodal status, intermediate histological grade and intermediate Ki-67 had a significant influence on the use of EndoPredict(®). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10549-020-05688-1) contains supplementary material, which is available to authorized users. Springer US 2020-05-20 2020 /pmc/articles/PMC7275019/ /pubmed/32436145 http://dx.doi.org/10.1007/s10549-020-05688-1 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/.
spellingShingle Clinical Trial
Almstedt, K.
Mendoza, S.
Otto, M.
Battista, M. J.
Steetskamp, J.
Heimes, A. S.
Krajnak, S.
Poplawski, A.
Gerhold-Ay, A.
Hasenburg, A.
Denkert, C.
Schmidt, M.
EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer
title EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer
title_full EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer
title_fullStr EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer
title_full_unstemmed EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer
title_short EndoPredict(®) in early hormone receptor-positive, HER2-negative breast cancer
title_sort endopredict(®) in early hormone receptor-positive, her2-negative breast cancer
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275019/
https://www.ncbi.nlm.nih.gov/pubmed/32436145
http://dx.doi.org/10.1007/s10549-020-05688-1
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