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EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES

Given availability of central nervous system (CNS)-penetrant systemic therapies that target the androgen receptor (AR), we evaluated the expression of the AR “target” in breast cancer brain metastases (BrM). METHODS: An established, retrospective cohort of 57 patients with metastatic breast cancer w...

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Autores principales: Fan, Kevin Yijun, Chehade, Rania, Qazi, Maleeha A, Moravan, Veronika, Nofech-Moses, Sharon, Jerzak, Katarzyna J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337554/
http://dx.doi.org/10.1093/noajnl/vdad071.011
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author Fan, Kevin Yijun
Chehade, Rania
Qazi, Maleeha A
Moravan, Veronika
Nofech-Moses, Sharon
Jerzak, Katarzyna J
author_facet Fan, Kevin Yijun
Chehade, Rania
Qazi, Maleeha A
Moravan, Veronika
Nofech-Moses, Sharon
Jerzak, Katarzyna J
author_sort Fan, Kevin Yijun
collection PubMed
description Given availability of central nervous system (CNS)-penetrant systemic therapies that target the androgen receptor (AR), we evaluated the expression of the AR “target” in breast cancer brain metastases (BrM). METHODS: An established, retrospective cohort of 57 patients with metastatic breast cancer who underwent surgery for BrM at the Sunnybrook Odette Cancer Centre (SOCC) between 1999 and 2013 was studied. AR expression in BrM samples was assessed in triplicate using immunohistochemistry (IHC). AR positive status was defined as nuclear AR expression ≥10% in tumor-infiltrating cells as a percentage of tumor area using the SP107 antibody. RESULTS: The median age of patients was 52 years (range 32-85 years). 17 (30%) patients had hormone receptor positive (HR+) /HER2-negative, 28 (49%) had HER2+, and 12 (21%) had triple negative breast cancer (TNBC) BrM. The median expression of AR was 20% (CI 1.6-38.3%) and 32 of 57 (56%) BrM were AR positive based on a cut-point of ≥10%. A significantly smaller proportion of patients with TNBC had AR+ BrM (n=2/12, 17%), compared to patients with HR+/HER2-ve (n= 9/17, 53%) or HER2+ (n=21/28, 75%) disease (p=0.04). Patients with AR positive versus AR negative BrM had similar overall survival (12.5 vs. 7.9 months, p= 0.6), brain-specific progression-free survival (8.0 vs. 5.1 months, p= 0.95), and time from breast cancer diagnosis to BrM diagnosis (51 vs. 29 months, p=0.16). CONCLUSION: AR is expressed in the majority of breast cancer BrM and represents a promising therapeutic target.
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spelling pubmed-103375542023-07-13 EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES Fan, Kevin Yijun Chehade, Rania Qazi, Maleeha A Moravan, Veronika Nofech-Moses, Sharon Jerzak, Katarzyna J Neurooncol Adv Posters Given availability of central nervous system (CNS)-penetrant systemic therapies that target the androgen receptor (AR), we evaluated the expression of the AR “target” in breast cancer brain metastases (BrM). METHODS: An established, retrospective cohort of 57 patients with metastatic breast cancer who underwent surgery for BrM at the Sunnybrook Odette Cancer Centre (SOCC) between 1999 and 2013 was studied. AR expression in BrM samples was assessed in triplicate using immunohistochemistry (IHC). AR positive status was defined as nuclear AR expression ≥10% in tumor-infiltrating cells as a percentage of tumor area using the SP107 antibody. RESULTS: The median age of patients was 52 years (range 32-85 years). 17 (30%) patients had hormone receptor positive (HR+) /HER2-negative, 28 (49%) had HER2+, and 12 (21%) had triple negative breast cancer (TNBC) BrM. The median expression of AR was 20% (CI 1.6-38.3%) and 32 of 57 (56%) BrM were AR positive based on a cut-point of ≥10%. A significantly smaller proportion of patients with TNBC had AR+ BrM (n=2/12, 17%), compared to patients with HR+/HER2-ve (n= 9/17, 53%) or HER2+ (n=21/28, 75%) disease (p=0.04). Patients with AR positive versus AR negative BrM had similar overall survival (12.5 vs. 7.9 months, p= 0.6), brain-specific progression-free survival (8.0 vs. 5.1 months, p= 0.95), and time from breast cancer diagnosis to BrM diagnosis (51 vs. 29 months, p=0.16). CONCLUSION: AR is expressed in the majority of breast cancer BrM and represents a promising therapeutic target. Oxford University Press 2023-07-12 /pmc/articles/PMC10337554/ http://dx.doi.org/10.1093/noajnl/vdad071.011 Text en © The Author(s) 2023. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Posters
Fan, Kevin Yijun
Chehade, Rania
Qazi, Maleeha A
Moravan, Veronika
Nofech-Moses, Sharon
Jerzak, Katarzyna J
EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES
title EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES
title_full EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES
title_fullStr EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES
title_full_unstemmed EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES
title_short EXPRESSION OF ANDROGEN RECEPTOR IN BREAST CANCER BRAIN METASTASES
title_sort expression of androgen receptor in breast cancer brain metastases
topic Posters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337554/
http://dx.doi.org/10.1093/noajnl/vdad071.011
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