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Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer

Breast cancer (BC) is the most common malignancy among women in Canada. Adjuvant treatment in early BC can reduce the risk of BC recurrence. Historically, the decision for adjuvant chemotherapy for early BC was made only based on clinical and tumour characteristics. In recent years, there has been a...

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Autores principales: Pauls, Mehrnoosh, Chia, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325032/
https://www.ncbi.nlm.nih.gov/pubmed/35877267
http://dx.doi.org/10.3390/curroncol29070407
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author Pauls, Mehrnoosh
Chia, Stephen
author_facet Pauls, Mehrnoosh
Chia, Stephen
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description Breast cancer (BC) is the most common malignancy among women in Canada. Adjuvant treatment in early BC can reduce the risk of BC recurrence. Historically, the decision for adjuvant chemotherapy for early BC was made only based on clinical and tumour characteristics. In recent years, there has been an effort toward developing genomic assays as a predictive and prognostic tool to improve precision in estimating disease recurrence, sensitivity to systemic treatment and ultimately with clinical utility for guidance regarding adjuvant systemic treatment(s). There are various commercial genomic tests available for early-stage ER+/HER-2 negative BC. This paper will review the Oncotype DX 21-gene Recurrence Score (RS), MammaPrint, EndoPredict, Prosigna(®), and Breast Cancer Index (BCI) genomic assays. We will also focus on these genomic assays’ clinical application and utility in node-positive early-stage BC based on the most recent evidence and guidance recommendations.
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spelling pubmed-93250322022-07-27 Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer Pauls, Mehrnoosh Chia, Stephen Curr Oncol Review Breast cancer (BC) is the most common malignancy among women in Canada. Adjuvant treatment in early BC can reduce the risk of BC recurrence. Historically, the decision for adjuvant chemotherapy for early BC was made only based on clinical and tumour characteristics. In recent years, there has been an effort toward developing genomic assays as a predictive and prognostic tool to improve precision in estimating disease recurrence, sensitivity to systemic treatment and ultimately with clinical utility for guidance regarding adjuvant systemic treatment(s). There are various commercial genomic tests available for early-stage ER+/HER-2 negative BC. This paper will review the Oncotype DX 21-gene Recurrence Score (RS), MammaPrint, EndoPredict, Prosigna(®), and Breast Cancer Index (BCI) genomic assays. We will also focus on these genomic assays’ clinical application and utility in node-positive early-stage BC based on the most recent evidence and guidance recommendations. MDPI 2022-07-20 /pmc/articles/PMC9325032/ /pubmed/35877267 http://dx.doi.org/10.3390/curroncol29070407 Text en © 2022 by the authors. https://creativecommons.org/licenses/by-nc/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC-BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Review
Pauls, Mehrnoosh
Chia, Stephen
Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer
title Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer
title_full Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer
title_fullStr Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer
title_full_unstemmed Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer
title_short Clinical Utility of Genomic Assay in Node-Positive Early-Stage Breast Cancer
title_sort clinical utility of genomic assay in node-positive early-stage breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325032/
https://www.ncbi.nlm.nih.gov/pubmed/35877267
http://dx.doi.org/10.3390/curroncol29070407
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