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Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer
Neoadjuvant chemotherapy (NACT) is used in locally advanced breast cancer to reduce tumour burden prior to surgical resection. However, only a subset of NACT treated patients will respond to treatment or achieve a pathologic complete response (pCR). This multicenter, prospective study (CTRIAL-IE (IC...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408914/ https://www.ncbi.nlm.nih.gov/pubmed/32645898 http://dx.doi.org/10.3390/cancers12071820 |
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author | McGuire, Andrew Casey, Maire-Caitlin Waldron, Ronan M. Heneghan, Helen Kalinina, Olga Holian, Emma McDermott, Ailbhe Lowery, Aoife J. Newell, John Dwyer, Róisín M. Miller, Nicola Keane, Maccon Brown, James A.L. Kerin, Michael J. |
author_facet | McGuire, Andrew Casey, Maire-Caitlin Waldron, Ronan M. Heneghan, Helen Kalinina, Olga Holian, Emma McDermott, Ailbhe Lowery, Aoife J. Newell, John Dwyer, Róisín M. Miller, Nicola Keane, Maccon Brown, James A.L. Kerin, Michael J. |
author_sort | McGuire, Andrew |
collection | PubMed |
description | Neoadjuvant chemotherapy (NACT) is used in locally advanced breast cancer to reduce tumour burden prior to surgical resection. However, only a subset of NACT treated patients will respond to treatment or achieve a pathologic complete response (pCR). This multicenter, prospective study (CTRIAL-IE (ICORG) 10-11 study) evaluated circulating microRNA as novel non-invasive prognostic biomarkers of NACT response in breast cancer. Selected circulating microRNAs (Let-7a, miR-21, miR-145, miR-155, miR-195) were quantified from patients undergoing standard of care NACT treatment (n = 114) from whole blood at collected at diagnosis, and the association with NACT response and clinicopathological features evaluated. NACT responders had significantly lower levels of miR-21 (p = 0.036) and miR-195 (p = 0.017), compared to non-responders. Evaluating all breast cancer cases miR-21 was found to be an independent predictor of response (OR 0.538, 95% CI 0.308–0.943, p < 0.05). Luminal cancer NACT responders were found to have significantly decreased levels of miR-145 (p = 0.033) and miR-21 (p = 0.048), compared to non-responders. This study demonstrates the prognostic ability of miR-21, miR-195 and miR-145 as circulating biomarkers stratifying breast cancer patients by NACT response, identifying patients that will derive the maximum benefit from chemotherapy. |
format | Online Article Text |
id | pubmed-7408914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74089142020-08-13 Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer McGuire, Andrew Casey, Maire-Caitlin Waldron, Ronan M. Heneghan, Helen Kalinina, Olga Holian, Emma McDermott, Ailbhe Lowery, Aoife J. Newell, John Dwyer, Róisín M. Miller, Nicola Keane, Maccon Brown, James A.L. Kerin, Michael J. Cancers (Basel) Article Neoadjuvant chemotherapy (NACT) is used in locally advanced breast cancer to reduce tumour burden prior to surgical resection. However, only a subset of NACT treated patients will respond to treatment or achieve a pathologic complete response (pCR). This multicenter, prospective study (CTRIAL-IE (ICORG) 10-11 study) evaluated circulating microRNA as novel non-invasive prognostic biomarkers of NACT response in breast cancer. Selected circulating microRNAs (Let-7a, miR-21, miR-145, miR-155, miR-195) were quantified from patients undergoing standard of care NACT treatment (n = 114) from whole blood at collected at diagnosis, and the association with NACT response and clinicopathological features evaluated. NACT responders had significantly lower levels of miR-21 (p = 0.036) and miR-195 (p = 0.017), compared to non-responders. Evaluating all breast cancer cases miR-21 was found to be an independent predictor of response (OR 0.538, 95% CI 0.308–0.943, p < 0.05). Luminal cancer NACT responders were found to have significantly decreased levels of miR-145 (p = 0.033) and miR-21 (p = 0.048), compared to non-responders. This study demonstrates the prognostic ability of miR-21, miR-195 and miR-145 as circulating biomarkers stratifying breast cancer patients by NACT response, identifying patients that will derive the maximum benefit from chemotherapy. MDPI 2020-07-07 /pmc/articles/PMC7408914/ /pubmed/32645898 http://dx.doi.org/10.3390/cancers12071820 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article McGuire, Andrew Casey, Maire-Caitlin Waldron, Ronan M. Heneghan, Helen Kalinina, Olga Holian, Emma McDermott, Ailbhe Lowery, Aoife J. Newell, John Dwyer, Róisín M. Miller, Nicola Keane, Maccon Brown, James A.L. Kerin, Michael J. Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer |
title | Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer |
title_full | Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer |
title_fullStr | Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer |
title_full_unstemmed | Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer |
title_short | Prospective Assessment of Systemic MicroRNAs as Markers of Response to Neoadjuvant Chemotherapy in Breast Cancer |
title_sort | prospective assessment of systemic micrornas as markers of response to neoadjuvant chemotherapy in breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408914/ https://www.ncbi.nlm.nih.gov/pubmed/32645898 http://dx.doi.org/10.3390/cancers12071820 |
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