LONGITUDINAL EVALUATION OF THE COMPLEXED-TO-TOTAL PROSTATE-SPECIFIC ANTIGEN RATIO IN MEN WITH PROSTATE DISEASE - EFFECT OF TREATMENT

Citation
F. Espana et al., LONGITUDINAL EVALUATION OF THE COMPLEXED-TO-TOTAL PROSTATE-SPECIFIC ANTIGEN RATIO IN MEN WITH PROSTATE DISEASE - EFFECT OF TREATMENT, European journal of cancer, 34(9), 1998, pp. 1375-1380
Citations number
29
Categorie Soggetti
Oncology
Journal title
ISSN journal
09598049
Volume
34
Issue
9
Year of publication
1998
Pages
1375 - 1380
Database
ISI
SICI code
0959-8049(1998)34:9<1375:LEOTCP>2.0.ZU;2-G
Abstract
The longitudinal changes in the complexed-to-total prostate specific a ntigen (PSA) ratio were evaluated in 90 men with benign prostatic hype rplasia (BPH) and 50 men with prostate cancer. The influence of treatm ent on this ratio was studied in 45 BPH patients and 50 patients with prostate cancer. Using a cut-off of 0.80 for the complexed-to-total PS A ratio, the large majority of prostate cancer patients had a ratio ab ove the cut-off before treatment in serial determinations, whereas mos t BPH patients had a ratio consistently below that value. However, the few prostate cancer patients who had a ratio less than or equal to 0. 80 showed this low ratio in serial determinations, as did BPH patients who had a ratio greater than or equal to 0.80. During treatment, the ratio significantly decreased in 43 of the 50 patients with prostate c ancer in parallel with the decrease in total PSA, and 34 of the 41 pat ients that had a pretreatment ratio > 0.80 showed a ratio less than or equal to 0.80 during hormonal therapy. Our results show that neither the physiological changes in total and complexed PSA nor the treatment of BPH patients change the diagnostic efficacy of the complexed-to-to tal PSA ratio, whereas in prostate cancer patients under hormonal ther apy, the ratio decreased in parallel with the decrease in total PSA. T his suggests that, apart from improving the diagnostic efficacy of tot al PSA, the complexed-to-total PSA ratio could also be used to monitor BPH patients for newly developed tumours or to monitor therapy in pat ients with prostate cancer. (C) 1998 Elsevier Science Ltd. All rights reserved.