FREE AND TOTAL SERUM PSA VALUES IN PATIENTS WITH PROSTATIC INTRAEPITHELIAL NEOPLASIA (PIN), PROSTATE-CANCER AND BPH - IS F T PSA A POTENTIAL PROBE FOR DORMANT AND MANIFEST CANCER/

Authors
Citation
M. Tarle et I. Kraljic, FREE AND TOTAL SERUM PSA VALUES IN PATIENTS WITH PROSTATIC INTRAEPITHELIAL NEOPLASIA (PIN), PROSTATE-CANCER AND BPH - IS F T PSA A POTENTIAL PROBE FOR DORMANT AND MANIFEST CANCER/, Anticancer research, 17(3A), 1997, pp. 1531-1534
Citations number
14
Categorie Soggetti
Oncology
Journal title
ISSN journal
02507005
Volume
17
Issue
3A
Year of publication
1997
Pages
1531 - 1534
Database
ISI
SICI code
0250-7005(1997)17:3A<1531:FATSPV>2.0.ZU;2-1
Abstract
Free and total PSA serum concentrations were retrospectively measured in 106 subjects: 45 patients with intraepithelial prostatic neoplasia (PIN), 30 subjects with benign prostatic hypertrophy (BPH) and 31 subj ects with untreated prostatic carcinoma. The (F/T)x100 PSA value is re corded in subjects with the elevated total PSA level (>4 ng/ml). PIN p atients were divided into two groups: a low grade PIN (PIN I) and high grade PIN (PIN II-III) patients. The mean (F/T)x100 PSA value in low grade PIN patients was 27.9+/-16.2 (range 17.1-41.2, median 25.1) and has been numerically similar to the respective value in BPH subjects ( 29.1+/-13.2, 15.8-48.0, 27.7). These parameters differed markedly (P<0 .01) from the mean (F/T)x100 PSA value in high grade PIN patients (16. 9+/-9.0, range 9.9-24.9, median 16.5). The later values were in turn c omparable (P>>0.05) with the respective value measured in untreated pr ostate cancer patients (14.4+/-10.8, 6.6-21.4, 126). Hence, values der ived from the measurement of free and total serum PSA level may distin guish low grade PIN that prevailingly remains latent disease from high grade PIN that is in most cases not only early prostatic carcinoma bu t that is often a precursor of an aggressive neoplasm. The published l iterature is incoherent regarding the influence of tumor spread on F/T PSA level. The cutoff point that divides BPH from cancer may depend o n tumor stage. We have nor investigated FIT PSA values related to diff erent stages and grades of prostate cancer. The cutoff point of (F/T)x 100 PSA in our study that divides malignant from benign prostate, or l atent from manifest cancer, was tentatively assigned as 18 with a spec ificity of 91% and selectivity of 69%. Our data are based on the appli cation of the CIS assay that according to the literature, gives higher F-PSA % compared to other respective kits.