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The androgen receptor as a surrogate marker for molecular apocrine breast cancer subtyping.

ΤίτλοςThe androgen receptor as a surrogate marker for molecular apocrine breast cancer subtyping.
Publication TypeJournal Article
Year of Publication2014
AuthorsLakis, S., Kotoula V., Eleftheraki A. G., Batistatou A., Bobos M., Koletsa T., Timotheadou E., Chrisafi S., Pentheroudakis G., Koutras A., Zagouri F., Linardou H., & Fountzilas G.
JournalBreast
Volume23
Issue3
Pagination234-43
Date Published2014 Jun
ISSN1532-3080
Λέξεις κλειδιάAndrogen Receptor Antagonists, Antineoplastic Agents, Antineoplastic Combined Chemotherapy Protocols, Biomarkers, Tumor, Breast Neoplasms, Chemotherapy, Adjuvant, Female, Humans, Middle Aged, Neoplasm Grading, Neoplasm Recurrence, Local, Prognosis, Receptors, Androgen, Receptors, Estrogen, Risk Assessment, Survival Analysis, Taxoids
Abstract

The Androgen Receptor (AR) is a potential prognostic marker and therapeutic target in breast cancer. We evaluated AR protein expression in high-risk breast cancer treated in the adjuvant setting. Tumors were subtyped into luminal (ER+/PgR±/AR±), molecular apocrine (MAC, [ER-/PgR-/AR+]) and hormone receptor negative carcinomas (HR-negative, [ER-/PgR-/AR-]). Subtyping was evaluated with respect to prognosis and to taxane therapy. High histologic grade (p < 0.001) and increased proliferation (p = 0.001) more often appeared in MAC and HR-negative than in luminal tumors. Patients with MAC had outcome comparable to the luminal group, while patients with HR-negative disease had increased risk for relapse and death. MAC outcome was favorable upon taxane-containing treatment; this remained significant upon multivariate analysis for overall survival (HR 0.31, 95%CI 0.13-0.74, interaction p = 0.035) and as a trend for time to relapse (p = 0.15). In conclusion, AR-related subtyping of breast cancer may be prognostic and serve for selecting optimal treatment combinations.

DOI10.1016/j.breast.2014.02.013
Alternate JournalBreast
PubMed ID24703723

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