[Correct use of prostate-specific antigen in office practice]

Prog Urol. 2008 Jan;18(1):41-5. doi: 10.1016/j.purol.2007.10.005. Epub 2008 Feb 15.
[Article in French]

Abstract

Objective: To standardize interpretation and comments of prostate-specific antigen (PSA) assay results by clinical pathology laboratories in office practice.

Material: From September 2004 to May 2006, interpretation and comments of PSA assay results performed by 100 different laboratories were analysed retrospectively.

Results: Nineteen different PSA assay kits were used. The so-called "normal" value for total PSA was less than 4 ng/ml for two-thirds of kits. Determination of the free PSA/total PSA ratio (91 cases) was based on a cut-off value ranging from 10 to 25% and the frequent laboratory comments (89 cases) more often referred to benign prostatic hyperplasia (51 case) than prostate cancer (nine cases).

Conclusion: The marked diversity of PSA assay techniques currently used and the divergent interpretations by various laboratories lead to problems of interpretation for both practitioners and patients.

Publication types

  • Comparative Study
  • English Abstract

MeSH terms

  • Humans
  • Laboratories / standards
  • Male
  • Prostate-Specific Antigen / blood*
  • Reagent Kits, Diagnostic / standards
  • Reference Values
  • Reproducibility of Results

Substances

  • Reagent Kits, Diagnostic
  • Prostate-Specific Antigen