Androgen Receptor Is Expressed in the Majority of Breast Cancer Brain Metastases and Is Subtype-Dependent

Author:

Fan Kevin Yijun1ORCID,Chehade Rania2,Qazi Maleeha1,Moravan Veronika3,Nofech-Mozes Sharon4,Jerzak Katarzyna J.5

Affiliation:

1. Faculty of Medicine, University of Toronto, Toronto, ON M5S1A8, Canada

2. Department of Medical Oncology, Faculty of Medicine, University of Toronto, Toronto, ON M5S1A8, Canada

3. VM Stats, Toronto, ON M5A4R3, Canada

4. Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON M5G1X5, Canada

5. Sunnybrook Odette Cancer Centre, University of Toronto, Toronto, ON M4N3M5, Canada

Abstract

We aimed to evaluate the expression of the “targetable” androgen receptor (AR) in breast cancer brain metastases (BrM). An established, retrospective 57-patient cohort with metastatic breast cancer who underwent surgery for BrM at the Sunnybrook Odette Cancer Centre between 1999–2013 was studied. AR expression in BrM samples was assessed in triplicate using immunohistochemistry (IHC). AR positive status was defined as nuclear AR expression ≥ 10% by IHC using the SP107 antibody. The median age of patients was 52 years (range 32–85 years). 28 (49%) of BrM were HER2+, 17 (30%) were hormone receptor positive (HR+)/HER2−, and 12 (21%) were triple negative breast cancers (TNBCs). 56% (n = 32/57) of BrM were AR positive, and median AR expression was 20% (CI 1.6–38.3%). AR expression was different across breast cancer subtypes; AR was most frequently expressed in HER2+ (n = 21/28), followed by HR+/HER2− (n = 9/17), and lowest in TNBC (n = 2/12) BrM (p = 0.003). 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). AR is expressed in the majority of breast cancer BrM and represents a potential therapeutic target.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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