COMPARISON OF PROSTATE SECRETORY PROTEIN WITH PROSTATE-SPECIFIC ANTIGEN AND PROSTATIC ACID-PHOSPHATASE AS A SERUM BIOMARKER FOR DIAGNOSIS AND MONITORING PATIENTS WITH PROSTATE CARCINOMA

Citation
Cl. Huang et al., COMPARISON OF PROSTATE SECRETORY PROTEIN WITH PROSTATE-SPECIFIC ANTIGEN AND PROSTATIC ACID-PHOSPHATASE AS A SERUM BIOMARKER FOR DIAGNOSIS AND MONITORING PATIENTS WITH PROSTATE CARCINOMA, The Prostate, 23(3), 1993, pp. 201-212
Citations number
31
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
02704137
Volume
23
Issue
3
Year of publication
1993
Pages
201 - 212
Database
ISI
SICI code
0270-4137(1993)23:3<201:COPSPW>2.0.ZU;2-I
Abstract
Serum prostate secretory protein (PSP) levels were measured in 49 pati ents with benign prostatic hyperplasia (BPH), 144 patients with variou s stages of prostatic carcinoma (Cap), and 82 CaP patients who were fo llowed serially. PSP values were compared with serum levels of prostat e specific antigen (PSA) and prostatic acid phosphatase (PAP). In the BPH group, PSP was elevated (> 10 ng/ml) in 41% of patients, whereas P SA (> 4 ng/ml) and PAP (> 3.3 ng/ml) were elevated in 39% and 23% of t he cases, respectively. PSP levels were elevated in 48% of the CaP pre treatment specimens, compared to 79% for PSA and 40% for PAP. PSP leve ls in cancer patients who had intracapsular disease were about two to three times higher than those observed for PAP. PSP was found to be th e only marker elevated in eight (6%) pretreatment CaP patient serum sp ecimens, while PAP was never found to be elevated when PSA was normal. PSP serum concentrations correlated with the clinical course of the d isease in 79% of patients, compared with 90% for PSA and 66% for PAP. In certain patients, monitored over time, disease correlation was refl ected in serum values with only a single biomarker, i.e., 1% with PAP, 8% with PSP, and 10% with PSA. This study has shown that PSP is a les s sensitive serum biomarker than PSA, but more sensitive than PAP for detection and monitoring the early stages of prostate cancer. This sug gests that PSP as a biomarker may be a useful adjunct for the manageme nt of a subpopulation of low-stage and -grade CaP. (C) 1993 Wiley-Liss , Inc.