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Annals of Surgical Oncology, Vol 1, Issue 6 495-503, Copyright © 1994 by Society of Surgical Oncology
ARTICLES |
L. P. Pertschuk, R. J. Macchia, J. G. Feldman, K. A. Brady, M. Levine, D. S. Kim, K. B. Eisenberg, E. Rainford, G. S. Prins and G. L. Greene
Department of Pathology, State University of New York, Brooklyn.
BACKGROUND: Numerous problems are associated with biochemical androgen receptor (AR) assay performance and interpretation in prostatic cancer. The purpose of this study was to determine if a novel immunocytochemical AR assay performed on intact tissue sections would prove useful in prognosticating endocrine response and survival. METHODS: A prospective study was done on 63 prostatic carcinomas maintained in liquid nitrogen for over a decade. The study used the peroxidase-antiperoxidase system and a polyclonal anti-AR antibody. RESULTS: Marked tissue and cellular heterogeneity of nuclear AR was apparent. A cut-off of 10% AR-positive cells maximized assay prognostic efficiency. Frequency of positivity was 48% and correlated significantly with endocrine response (p = 0.03), time to progression (p = 0.0016), and survival (p = 0.02), but not with grade, stage, or ethnicity. CONCLUSIONS: This AR assay could be prognostically useful in the clinical management of prostate cancer and is suitable for use in the community hospital laboratory.
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