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[Cancer Research 55, 2104-2110, May 15, 1995]
© 1995 American Association for Cancer Research

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Prostate-specific Antigen Is a New Favorable Prognostic Indicator for Women with Breast Cancer1

He Yu, Maurizia Giai, Eleftherios P. Diamandis2, Dionyssios Katsaros, Donald J. A. Sutherland, Michael A. Levesque, Riccardo Roagna, Riccardo Ponzone and Piero Sismondi

Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, and Department of Clinical Biochemistry, University of Toronto, Toronto, Ontario, Canada M5G 1X5 [H. Y., E. P. D., M. A. L.]; Department of Gynecologic Oncology, Institute of Obstetrics and Gynecology, University of Turin, 10121 Turin, Italy [M. G., D. K., R. R., R. P., P. S.]; and Toronto Bayview Regional Cancer Centre, Sunnybrook Health Centre, Toronto, Ontario M4N 3M5, Canada [J. A. S.]

Prostate-specific antigen (PSA) is thought to be produced exclusively by prostatic epithelial cells and is currently used as a tumor marker of prostatic adenocarcinoma. We recently found that 30% of breast cancers contain PSA immunoreactivity (IR-PSA). To examine the prognostic value of PSA in female breast cancer, we measured IR-PSA in tumor cytosols of 174 breast cancer patients and classified the breast cancers as either PSA positive or PSA negative based on an IR-PSA cutoff level of 0.03 ng/mg. IR-PSA was present in 27% of the patients. IR-PSA presence was associated with early disease stage, small tumors, and estrogen receptor-positive tumors. We used the Cox proportional hazards regression model to analyze survival of patients in association with PSA status and found that patients with IR-PSA-positive tumors had a reduced risk for relapse and death in univariate analysis (P = 0.02 and 0.06, respectively) and a reduced risk for relapse in multivariate analysis (P = 0.03). Further analysis indicated that the effect of IR-PSA on relapse-free survival was evident in node-positive or estrogen receptor-negative patients. Our study suggests that IR-PSA is an independent favorable prognostic marker for breast cancer and may be used to identify a subgroup of estrogen receptor-negative and/or node-positive patients who have good prognoses.

1 This work was supported by a Cancer Research Society, Inc. (Montreal, Canada) grant (E. P. D.) and the University Research Incentive Fund of the Province of Ontario (E. P. D.). D. K. is supported by an Associazione Italiana per la Ricerca sul Cancro fellowship.

2 To whom requests for reprints should be addressed, at Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario M5G 1X5, CANADA.

Received 12/16/94. Accepted 3/16/95.




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Copyright © 1995 by the American Association for Cancer Research.