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Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy

BACKGROUND: Women with atypical hyperplasia (AH) is associated with a higher risk of future breast cancer. However, whether AH found at margins in patients with breast-conserving surgery (BCS) after neoadjuvant chemotherapy (NAC) needs re-excision is not well-defined. The aim of the present study wa...

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Autores principales: Su, An, Zhang, Jing, Liu, Jieqiong, Yang, Yaping, He, Zhou, Bao, Haoshi, Deng, Heran, Wu, Jiannan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235679/
https://www.ncbi.nlm.nih.gov/pubmed/37274293
http://dx.doi.org/10.3389/fonc.2023.1202689
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author Su, An
Zhang, Jing
Liu, Jieqiong
Yang, Yaping
He, Zhou
Bao, Haoshi
Deng, Heran
Wu, Jiannan
author_facet Su, An
Zhang, Jing
Liu, Jieqiong
Yang, Yaping
He, Zhou
Bao, Haoshi
Deng, Heran
Wu, Jiannan
author_sort Su, An
collection PubMed
description BACKGROUND: Women with atypical hyperplasia (AH) is associated with a higher risk of future breast cancer. However, whether AH found at margins in patients with breast-conserving surgery (BCS) after neoadjuvant chemotherapy (NAC) needs re-excision is not well-defined. The aim of the present study was to evaluate the impact of AH at the surgical margins on the local recurrence and survival outcomes in breast cancer patients treated with NAC and BCS. METHODS: A retrospective analysis comparing patients who treated with NAC and BCS with AH at the margins to those without AH was performed. RESULTS: 598 patients were included in this study. The 5-year rates of ipsilateral breast tumor recurrence (IBTR) were 4.6% and 6.2% in patients with and without AH, respectively. No significant differences were observed among the two groups in terms of IBTR, DMFS, or OS. HER2 overexpressing breast cancer patients with severe AH at margins have a significantly higher risk of IBTR compared to those without severe AH. CONCLUSION: Our study suggests that the presence of AH at the surgical margins of BCS in patients who received NAC does not appear to increase the risk of ipsilateral breast cancer. Therefore, there is no need for surgeons to routinely perform additional re-excision of AH found at the margins of BCS in these patients. However, selective re-excision should be considered in certain cases, particularly in patients with HER2 overexpression.
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spelling pubmed-102356792023-06-03 Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy Su, An Zhang, Jing Liu, Jieqiong Yang, Yaping He, Zhou Bao, Haoshi Deng, Heran Wu, Jiannan Front Oncol Oncology BACKGROUND: Women with atypical hyperplasia (AH) is associated with a higher risk of future breast cancer. However, whether AH found at margins in patients with breast-conserving surgery (BCS) after neoadjuvant chemotherapy (NAC) needs re-excision is not well-defined. The aim of the present study was to evaluate the impact of AH at the surgical margins on the local recurrence and survival outcomes in breast cancer patients treated with NAC and BCS. METHODS: A retrospective analysis comparing patients who treated with NAC and BCS with AH at the margins to those without AH was performed. RESULTS: 598 patients were included in this study. The 5-year rates of ipsilateral breast tumor recurrence (IBTR) were 4.6% and 6.2% in patients with and without AH, respectively. No significant differences were observed among the two groups in terms of IBTR, DMFS, or OS. HER2 overexpressing breast cancer patients with severe AH at margins have a significantly higher risk of IBTR compared to those without severe AH. CONCLUSION: Our study suggests that the presence of AH at the surgical margins of BCS in patients who received NAC does not appear to increase the risk of ipsilateral breast cancer. Therefore, there is no need for surgeons to routinely perform additional re-excision of AH found at the margins of BCS in these patients. However, selective re-excision should be considered in certain cases, particularly in patients with HER2 overexpression. Frontiers Media S.A. 2023-05-19 /pmc/articles/PMC10235679/ /pubmed/37274293 http://dx.doi.org/10.3389/fonc.2023.1202689 Text en Copyright © 2023 Su, Zhang, Liu, Yang, He, Bao, Deng and Wu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Su, An
Zhang, Jing
Liu, Jieqiong
Yang, Yaping
He, Zhou
Bao, Haoshi
Deng, Heran
Wu, Jiannan
Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy
title Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy
title_full Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy
title_fullStr Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy
title_full_unstemmed Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy
title_short Impact of Atypical Hyperplasia at Surgical Margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy
title_sort impact of atypical hyperplasia at surgical margins on breast cancer outcomes in patients treated with neoadjuvant chemotherapy
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235679/
https://www.ncbi.nlm.nih.gov/pubmed/37274293
http://dx.doi.org/10.3389/fonc.2023.1202689
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