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Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study

PURPOSE: To investigate the impact of metabolic syndrome (MetS) on pathologic complete response (pCR) and clinical outcomes in breast cancer (BC) patients who received neoadjuvant chemotherapy (NAC). METHODS: We analyzed 221 female BC patients at Harbin Medical University Cancer Hospital who receive...

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Autores principales: Zhou, Zhaoyue, Zhang, Yue, Li, Yue, Jiang, Cong, Wu, Yang, Shang, Lingmin, Huang, Yuanxi, Cheng, Shaoqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845900/
https://www.ncbi.nlm.nih.gov/pubmed/36686748
http://dx.doi.org/10.3389/fonc.2022.1080054
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author Zhou, Zhaoyue
Zhang, Yue
Li, Yue
Jiang, Cong
Wu, Yang
Shang, Lingmin
Huang, Yuanxi
Cheng, Shaoqiang
author_facet Zhou, Zhaoyue
Zhang, Yue
Li, Yue
Jiang, Cong
Wu, Yang
Shang, Lingmin
Huang, Yuanxi
Cheng, Shaoqiang
author_sort Zhou, Zhaoyue
collection PubMed
description PURPOSE: To investigate the impact of metabolic syndrome (MetS) on pathologic complete response (pCR) and clinical outcomes in breast cancer (BC) patients who received neoadjuvant chemotherapy (NAC). METHODS: We analyzed 221 female BC patients at Harbin Medical University Cancer Hospital who received NAC and divided them into MetS and non-MetS groups according to National Cholesterol Education Program Adult Treatment Panel III (NCEP-ATP III) criteria to investigate the association between MetS and clinicopathological characteristics, pathologic response, and long-term survival and to observe the changes in metabolic parameters after NAC. RESULTS: A total of 53 (24.0%) BC patients achieved pCR after NAC in our study. MetS status was an independent predictor of pCR, and pCR was more difficult to obtain in the MetS group than the non-MetS group (P=0.028). All metabolic parameters deteriorated significantly after NAC, especially the blood lipid index (P<0.010). The median follow-up time was 6 years. After adjusting for other prognostic factors, MetS was found to be strongly associated with an increased risk of recurrence (P=0.007) and mortality (P=0.004) in BC patients receiving NAC. Compared to individuals without any MetS component, the risk of death and disease progression increased sharply as the number of MetS components increased. CONCLUSIONS: In BC patients who received NAC, MetS was associated with poor outcomes, including a lower pCR rate and increased risks of recurrence and mortality.
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spelling pubmed-98459002023-01-19 Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study Zhou, Zhaoyue Zhang, Yue Li, Yue Jiang, Cong Wu, Yang Shang, Lingmin Huang, Yuanxi Cheng, Shaoqiang Front Oncol Oncology PURPOSE: To investigate the impact of metabolic syndrome (MetS) on pathologic complete response (pCR) and clinical outcomes in breast cancer (BC) patients who received neoadjuvant chemotherapy (NAC). METHODS: We analyzed 221 female BC patients at Harbin Medical University Cancer Hospital who received NAC and divided them into MetS and non-MetS groups according to National Cholesterol Education Program Adult Treatment Panel III (NCEP-ATP III) criteria to investigate the association between MetS and clinicopathological characteristics, pathologic response, and long-term survival and to observe the changes in metabolic parameters after NAC. RESULTS: A total of 53 (24.0%) BC patients achieved pCR after NAC in our study. MetS status was an independent predictor of pCR, and pCR was more difficult to obtain in the MetS group than the non-MetS group (P=0.028). All metabolic parameters deteriorated significantly after NAC, especially the blood lipid index (P<0.010). The median follow-up time was 6 years. After adjusting for other prognostic factors, MetS was found to be strongly associated with an increased risk of recurrence (P=0.007) and mortality (P=0.004) in BC patients receiving NAC. Compared to individuals without any MetS component, the risk of death and disease progression increased sharply as the number of MetS components increased. CONCLUSIONS: In BC patients who received NAC, MetS was associated with poor outcomes, including a lower pCR rate and increased risks of recurrence and mortality. Frontiers Media S.A. 2023-01-04 /pmc/articles/PMC9845900/ /pubmed/36686748 http://dx.doi.org/10.3389/fonc.2022.1080054 Text en Copyright © 2023 Zhou, Zhang, Li, Jiang, Wu, Shang, Huang and Cheng 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
Zhou, Zhaoyue
Zhang, Yue
Li, Yue
Jiang, Cong
Wu, Yang
Shang, Lingmin
Huang, Yuanxi
Cheng, Shaoqiang
Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study
title Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study
title_full Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study
title_fullStr Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study
title_full_unstemmed Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study
title_short Metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: A case-control study
title_sort metabolic syndrome is a risk factor for breast cancer patients receiving neoadjuvant chemotherapy: a case-control study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845900/
https://www.ncbi.nlm.nih.gov/pubmed/36686748
http://dx.doi.org/10.3389/fonc.2022.1080054
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