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Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value

PURPOSE: There is cumulative evidence that changes in biomarker status occur frequently during the metastatic progression of breast cancer and affect treatment response. The purpose of this study was to evaluate the frequency of biomarker changes in metastatic breast cancer (MBC) and its impact on p...

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Autores principales: Woo, Ji Won, Chung, Yul Ri, Ahn, Soomin, Kang, Eunyoung, Kim, Eun-Kyu, Kim, Se Hyun, Kim, Jee Hyun, Kim, In Ah, Park, So Yeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Breast Cancer Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769393/
https://www.ncbi.nlm.nih.gov/pubmed/31598343
http://dx.doi.org/10.4048/jbc.2019.22.e38
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author Woo, Ji Won
Chung, Yul Ri
Ahn, Soomin
Kang, Eunyoung
Kim, Eun-Kyu
Kim, Se Hyun
Kim, Jee Hyun
Kim, In Ah
Park, So Yeon
author_facet Woo, Ji Won
Chung, Yul Ri
Ahn, Soomin
Kang, Eunyoung
Kim, Eun-Kyu
Kim, Se Hyun
Kim, Jee Hyun
Kim, In Ah
Park, So Yeon
author_sort Woo, Ji Won
collection PubMed
description PURPOSE: There is cumulative evidence that changes in biomarker status occur frequently during the metastatic progression of breast cancer and affect treatment response. The purpose of this study was to evaluate the frequency of biomarker changes in metastatic breast cancer (MBC) and its impact on prognosis. METHODS: A total of 152 patients diagnosed with MBC at the time of initial diagnosis or during post-surgical follow-up were included. Changes in biomarker status in MBCs, their frequency according to various metastatic sites, tumor characteristics, and their association with patient survival were analyzed. RESULTS: Estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), and Ki-67 status changed in 9 (6.0%), 40 (26.3%), 12 (7.9%), and 29 (19.1%) patients, respectively. ER, PR, and HER2 mainly showed positive to negative conversion, whereas Ki-67 changed mostly from a low to high index. There were no differences in the frequencies of biomarker changes according to the metastatic sites. As for ER and HER2, cases with negative conversion showed low expression levels in the primary tumor. Survival analyses indicated that a positive to negative conversion of ER was an independent poor prognostic factor in patients with primary ER-positive breast cancer. CONCLUSION: Changes in biomarker status are not rare, and usually occur in an unfavorable direction in breast cancer metastases. Negative conversion of ER status is a predictor of poor prognosis. Thus, it is beneficial to evaluate changes in biomarker status in MBC not only for the purpose of determining treatment options but also for prognostication of patients.
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spelling pubmed-67693932019-10-09 Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value Woo, Ji Won Chung, Yul Ri Ahn, Soomin Kang, Eunyoung Kim, Eun-Kyu Kim, Se Hyun Kim, Jee Hyun Kim, In Ah Park, So Yeon J Breast Cancer Original Article PURPOSE: There is cumulative evidence that changes in biomarker status occur frequently during the metastatic progression of breast cancer and affect treatment response. The purpose of this study was to evaluate the frequency of biomarker changes in metastatic breast cancer (MBC) and its impact on prognosis. METHODS: A total of 152 patients diagnosed with MBC at the time of initial diagnosis or during post-surgical follow-up were included. Changes in biomarker status in MBCs, their frequency according to various metastatic sites, tumor characteristics, and their association with patient survival were analyzed. RESULTS: Estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), and Ki-67 status changed in 9 (6.0%), 40 (26.3%), 12 (7.9%), and 29 (19.1%) patients, respectively. ER, PR, and HER2 mainly showed positive to negative conversion, whereas Ki-67 changed mostly from a low to high index. There were no differences in the frequencies of biomarker changes according to the metastatic sites. As for ER and HER2, cases with negative conversion showed low expression levels in the primary tumor. Survival analyses indicated that a positive to negative conversion of ER was an independent poor prognostic factor in patients with primary ER-positive breast cancer. CONCLUSION: Changes in biomarker status are not rare, and usually occur in an unfavorable direction in breast cancer metastases. Negative conversion of ER status is a predictor of poor prognosis. Thus, it is beneficial to evaluate changes in biomarker status in MBC not only for the purpose of determining treatment options but also for prognostication of patients. Korean Breast Cancer Society 2019-09-02 /pmc/articles/PMC6769393/ /pubmed/31598343 http://dx.doi.org/10.4048/jbc.2019.22.e38 Text en © 2019 Korean Breast Cancer Society https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Woo, Ji Won
Chung, Yul Ri
Ahn, Soomin
Kang, Eunyoung
Kim, Eun-Kyu
Kim, Se Hyun
Kim, Jee Hyun
Kim, In Ah
Park, So Yeon
Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value
title Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value
title_full Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value
title_fullStr Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value
title_full_unstemmed Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value
title_short Changes in Biomarker Status in Metastatic Breast Cancer and Their Prognostic Value
title_sort changes in biomarker status in metastatic breast cancer and their prognostic value
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769393/
https://www.ncbi.nlm.nih.gov/pubmed/31598343
http://dx.doi.org/10.4048/jbc.2019.22.e38
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