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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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