z-logo
Premium
Influence of high‐grade prostatic intra‐epithelial neoplasia on total and percentage free serum prostatic specific antigen
Author(s) -
Morote,
Gloria Encabo,
López López,
de Torres
Publication year - 1999
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1046/j.1464-410x.1999.00213.x
Subject(s) - medicine , urology , prostate cancer , rectal examination , prostate specific antigen , prostate , biopsy , cancer
Objective  To analyse the influence of high‐grade prostatic intra‐epithelial neoplasia (HGPIN) on total and percentage free serum prostatic specific antigen (PSA). Patients and methods The total and free serum PSA levels were measured (using a double‐monoclonal antibody immunoassay, Tandem and Tandem free PSA, Hybritech Inc, Liège, Belgium) in 570 consecutive patients undergoing sextant ultrasound‐guided prostatic biopsy because of an abnormal digital rectal examination or a serum PSA concentration of > 4.0 ng/mL. The main diagnosis was benign disease in 321 (56%) and prostate cancer in 249 (44%). HGPIN was detected in 85 (15%) of the patients; in 17 (20%) it was associated with benign tissue and in 68 (80%) with prostate cancer. Results Patients with benign disease had a median total serum PSA level of 7.2 with no HGPIN and 7.7 ng/mL when HGPIN was present ( P >0.05); the corresponding values in patients with prostate cancer were 16.0 and 15.9 ng/mL ( P >0.05). The median percentage free serum PSA was 15.8 in patients with HGPIN‐free benign disease and 14.1 when HGPIN was present ( P >0.05); the corresponding values in patients with prostate cancer were 9.7 and 11.0 ( P >0.05). In a multivariate analysis, prostate cancer was the major contributor to total and percentage free serum PSA levels. Conclusion The presence of HGPIN does not contribute significantly to total and percentage free serum PSA levels.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here