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Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer

BACKGROUND: The standard treatment of hormone receptor positive, HER2 negative early breast cancer (BC) is surgery followed by adjuvant systemic therapy either with endocrine therapy alone or with the addition of chemotherapy followed by endocrine therapy. Adjuvant systemic therapy reduces the risk...

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Autores principales: Ovcaricek, Tanja, Takac, Iztok, Matos, Erika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765159/
https://www.ncbi.nlm.nih.gov/pubmed/31553709
http://dx.doi.org/10.2478/raon-2019-0038
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author Ovcaricek, Tanja
Takac, Iztok
Matos, Erika
author_facet Ovcaricek, Tanja
Takac, Iztok
Matos, Erika
author_sort Ovcaricek, Tanja
collection PubMed
description BACKGROUND: The standard treatment of hormone receptor positive, HER2 negative early breast cancer (BC) is surgery followed by adjuvant systemic therapy either with endocrine therapy alone or with the addition of chemotherapy followed by endocrine therapy. Adjuvant systemic therapy reduces the risk of recurrence and death from BC. Whether an individual patient will benefit from adjuvant chemotherapy is an important clinical decision. Decisions that rely solely on clinical-pathological factors can often lead to overtreatment. Multigene signatures represent an important progress in optimal selection of high risk patients that might benefit from the addition of chemotherapy to adjuvant endocrine therapy. CONCLUSIONS: Several signatures are already commercially available and also accepted by international guidelines. Oncotype DX and MammaPrint have been most extensively validated and supported by level IA evidence.
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spelling pubmed-67651592019-10-15 Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer Ovcaricek, Tanja Takac, Iztok Matos, Erika Radiol Oncol Review BACKGROUND: The standard treatment of hormone receptor positive, HER2 negative early breast cancer (BC) is surgery followed by adjuvant systemic therapy either with endocrine therapy alone or with the addition of chemotherapy followed by endocrine therapy. Adjuvant systemic therapy reduces the risk of recurrence and death from BC. Whether an individual patient will benefit from adjuvant chemotherapy is an important clinical decision. Decisions that rely solely on clinical-pathological factors can often lead to overtreatment. Multigene signatures represent an important progress in optimal selection of high risk patients that might benefit from the addition of chemotherapy to adjuvant endocrine therapy. CONCLUSIONS: Several signatures are already commercially available and also accepted by international guidelines. Oncotype DX and MammaPrint have been most extensively validated and supported by level IA evidence. Sciendo 2019-09-24 /pmc/articles/PMC6765159/ /pubmed/31553709 http://dx.doi.org/10.2478/raon-2019-0038 Text en © 2019 Tanja Ovcaricek, Iztok Takac, Erika Matos, published by Sciendo http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Review
Ovcaricek, Tanja
Takac, Iztok
Matos, Erika
Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer
title Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer
title_full Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer
title_fullStr Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer
title_full_unstemmed Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer
title_short Multigene Expression Signatures in Early Hormone Receptor Positive HER 2 Negative Breast Cancer
title_sort multigene expression signatures in early hormone receptor positive her 2 negative breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765159/
https://www.ncbi.nlm.nih.gov/pubmed/31553709
http://dx.doi.org/10.2478/raon-2019-0038
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