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Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study

BACKGROUND AND AIMS: This study aimed to access possible relationships between breast cancer subtypes and sites of distant metastasis in breast cancer. RESULTS: A total of 243,896 patients, including 226,451 cases in control groups were identified. Bone metastasis was found in 8848 cases, compared w...

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Autores principales: Wu, Qi, Li, Juanjuan, Zhu, Shan, Wu, Juan, Chen, Chuang, Liu, Qian, Wei, Wen, Zhang, Yimin, Sun, Shengrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438624/
https://www.ncbi.nlm.nih.gov/pubmed/28427196
http://dx.doi.org/10.18632/oncotarget.15856
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author Wu, Qi
Li, Juanjuan
Zhu, Shan
Wu, Juan
Chen, Chuang
Liu, Qian
Wei, Wen
Zhang, Yimin
Sun, Shengrong
author_facet Wu, Qi
Li, Juanjuan
Zhu, Shan
Wu, Juan
Chen, Chuang
Liu, Qian
Wei, Wen
Zhang, Yimin
Sun, Shengrong
author_sort Wu, Qi
collection PubMed
description BACKGROUND AND AIMS: This study aimed to access possible relationships between breast cancer subtypes and sites of distant metastasis in breast cancer. RESULTS: A total of 243,896 patients, including 226,451 cases in control groups were identified. Bone metastasis was found in 8848 cases, compared with 1,000 brain metastasis cases, 3434 liver metastasis cases and 4167 lung metastasis cases. Patients with all subtypes were most prone to bone metastases, the incidence of bone metastasis in HR+/HER2+ subtype was up to 5.1 %. Further, HR−/HER2+ subtype patients had a higher probability of brain (OR = 1.978) metastasis compared to HR+/HER2− subtype patients. In addition, liver metastasis was more frequently observed in the HER2 positive subtypes compared with HER2 negative subtypes. Patients with TN primarily presented lung metastasis, but it made no difference in the probability of lung metastases of all subtypes. MATERIALS AND METHODS: Using the 2010–2013 Surveillance, Epidemiology, and End Results Program(SEER) data, a retrospective, population-based cohort study to investigate tumor subtypes-specific differences in the sites of distant metastasis. Metastatic patterns information was provided for bone, brain, liver and lung. The breast cancer was classified into four subtypes: hormone receptor (HR) +/ human epidermal growth factor receptor 2 (HER2) −, HR+/HER2+, HR−/HER2+ and triple negative (TN). CONCLUSIONS: The pathological subtypes of breast cancer are clearly different in metastatic behavior with regard to the sites of distant metastasis, emphasizing that this knowledge may help to determine the appropriate strategy for follow-up and guide personalized medicine.
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spelling pubmed-54386242017-05-24 Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study Wu, Qi Li, Juanjuan Zhu, Shan Wu, Juan Chen, Chuang Liu, Qian Wei, Wen Zhang, Yimin Sun, Shengrong Oncotarget Research Paper BACKGROUND AND AIMS: This study aimed to access possible relationships between breast cancer subtypes and sites of distant metastasis in breast cancer. RESULTS: A total of 243,896 patients, including 226,451 cases in control groups were identified. Bone metastasis was found in 8848 cases, compared with 1,000 brain metastasis cases, 3434 liver metastasis cases and 4167 lung metastasis cases. Patients with all subtypes were most prone to bone metastases, the incidence of bone metastasis in HR+/HER2+ subtype was up to 5.1 %. Further, HR−/HER2+ subtype patients had a higher probability of brain (OR = 1.978) metastasis compared to HR+/HER2− subtype patients. In addition, liver metastasis was more frequently observed in the HER2 positive subtypes compared with HER2 negative subtypes. Patients with TN primarily presented lung metastasis, but it made no difference in the probability of lung metastases of all subtypes. MATERIALS AND METHODS: Using the 2010–2013 Surveillance, Epidemiology, and End Results Program(SEER) data, a retrospective, population-based cohort study to investigate tumor subtypes-specific differences in the sites of distant metastasis. Metastatic patterns information was provided for bone, brain, liver and lung. The breast cancer was classified into four subtypes: hormone receptor (HR) +/ human epidermal growth factor receptor 2 (HER2) −, HR+/HER2+, HR−/HER2+ and triple negative (TN). CONCLUSIONS: The pathological subtypes of breast cancer are clearly different in metastatic behavior with regard to the sites of distant metastasis, emphasizing that this knowledge may help to determine the appropriate strategy for follow-up and guide personalized medicine. Impact Journals LLC 2017-03-02 /pmc/articles/PMC5438624/ /pubmed/28427196 http://dx.doi.org/10.18632/oncotarget.15856 Text en Copyright: © 2017 Wu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wu, Qi
Li, Juanjuan
Zhu, Shan
Wu, Juan
Chen, Chuang
Liu, Qian
Wei, Wen
Zhang, Yimin
Sun, Shengrong
Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study
title Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study
title_full Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study
title_fullStr Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study
title_full_unstemmed Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study
title_short Breast cancer subtypes predict the preferential site of distant metastases: a SEER based study
title_sort breast cancer subtypes predict the preferential site of distant metastases: a seer based study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438624/
https://www.ncbi.nlm.nih.gov/pubmed/28427196
http://dx.doi.org/10.18632/oncotarget.15856
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