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Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer
BACKGROUND: The aim of this study was to analyze the association of molecular subtype concordance and disease outcome in patients with synchronous bilateral breast cancer (SBBC) and metachronous breast cancer (MBBC). PATIENTS AND METHODS: Patients diagnosed with SBBC or MBBC in the Surveillance, Epi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027898/ https://www.ncbi.nlm.nih.gov/pubmed/33774461 http://dx.doi.org/10.1016/j.breast.2021.03.005 |
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author | Ding, Shuning Sun, Xi Lu, Shuangshuang Wang, Zheng Chen, Xiaosong Shen, Kunwei |
author_facet | Ding, Shuning Sun, Xi Lu, Shuangshuang Wang, Zheng Chen, Xiaosong Shen, Kunwei |
author_sort | Ding, Shuning |
collection | PubMed |
description | BACKGROUND: The aim of this study was to analyze the association of molecular subtype concordance and disease outcome in patients with synchronous bilateral breast cancer (SBBC) and metachronous breast cancer (MBBC). PATIENTS AND METHODS: Patients diagnosed with SBBC or MBBC in the Surveillance, Epidemiology, and End Results (SEER) database or Comprehensive Breast Health Center (CBHC) Ruijin Hospital, Shanghai were retrospectively reviewed and included. Clinicopathologic features, molecular subtype status concordance, and prognosis were compared in patients with SBBC and MBBC. Other prognostic factors for breast cancer-specific survival (BCSS) and overall survival (OS) were also identified for bilateral breast cancer patients. RESULTS: Totally, 3395 and 115 patients were included from the SEER and Ruijin CBHC cohorts. Molecular subtype concordance rate was higher in the SBBC group compared to MBBC in both SEER cohort (75.8% vs 57.7%, p < 0.001) and Ruijin CBHC cohort (76.2% vs 45.2%, p = 0.002). Survival analyses indicated that SBBC was related to worse BCSS than MBBC (p = 0.015). Molecular subtype discordance was related to worse BCSS (hazard ratio (HR), 1.64, 95% confidential interval (CI), 1.18–2.27, p = 0.003) and OS (HR, 1.59, 95% CI, 1.24–2.04, p < 0.001) in the SBBC group, but not for the MBBC group (p = 0.650 for BCSS, p = 0.669 for OS). CONCLUSIONS: Molecular subtype concordance rate was higher in the SBBC group than MBBC group. Patients with discordant molecular subtype was associated with worse disease outcome in the SBBC patients, but not in MBBC, which deserves further clinical evaluation. |
format | Online Article Text |
id | pubmed-8027898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80278982021-04-13 Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer Ding, Shuning Sun, Xi Lu, Shuangshuang Wang, Zheng Chen, Xiaosong Shen, Kunwei Breast Original Article BACKGROUND: The aim of this study was to analyze the association of molecular subtype concordance and disease outcome in patients with synchronous bilateral breast cancer (SBBC) and metachronous breast cancer (MBBC). PATIENTS AND METHODS: Patients diagnosed with SBBC or MBBC in the Surveillance, Epidemiology, and End Results (SEER) database or Comprehensive Breast Health Center (CBHC) Ruijin Hospital, Shanghai were retrospectively reviewed and included. Clinicopathologic features, molecular subtype status concordance, and prognosis were compared in patients with SBBC and MBBC. Other prognostic factors for breast cancer-specific survival (BCSS) and overall survival (OS) were also identified for bilateral breast cancer patients. RESULTS: Totally, 3395 and 115 patients were included from the SEER and Ruijin CBHC cohorts. Molecular subtype concordance rate was higher in the SBBC group compared to MBBC in both SEER cohort (75.8% vs 57.7%, p < 0.001) and Ruijin CBHC cohort (76.2% vs 45.2%, p = 0.002). Survival analyses indicated that SBBC was related to worse BCSS than MBBC (p = 0.015). Molecular subtype discordance was related to worse BCSS (hazard ratio (HR), 1.64, 95% confidential interval (CI), 1.18–2.27, p = 0.003) and OS (HR, 1.59, 95% CI, 1.24–2.04, p < 0.001) in the SBBC group, but not for the MBBC group (p = 0.650 for BCSS, p = 0.669 for OS). CONCLUSIONS: Molecular subtype concordance rate was higher in the SBBC group than MBBC group. Patients with discordant molecular subtype was associated with worse disease outcome in the SBBC patients, but not in MBBC, which deserves further clinical evaluation. Elsevier 2021-03-20 /pmc/articles/PMC8027898/ /pubmed/33774461 http://dx.doi.org/10.1016/j.breast.2021.03.005 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Ding, Shuning Sun, Xi Lu, Shuangshuang Wang, Zheng Chen, Xiaosong Shen, Kunwei Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer |
title | Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer |
title_full | Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer |
title_fullStr | Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer |
title_full_unstemmed | Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer |
title_short | Association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer |
title_sort | association of molecular subtype concordance and survival outcome in synchronous and metachronous bilateral breast cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027898/ https://www.ncbi.nlm.nih.gov/pubmed/33774461 http://dx.doi.org/10.1016/j.breast.2021.03.005 |
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