Validity of the prostate specific antigen test for prostate cancer screening: followup study with a bank of 21,000 sera in Finland

J Urol. 2001 Dec;166(6):2189-91; discussion 2191-2. doi: 10.1016/s0022-5347(05)65532-2.

Abstract

Purpose: We investigate the validity of prostate specific antigen (PSA) as a screening test for prostate cancer.

Materials and methods: A registry of serum samples drawn from 1968 to 1976 from 21,387 men was linked to the Finnish Cancer Registry. During followup from 1968 to 1991, 104 prostate cancers were identified. A matched case control design with incidence density sampling and nested in the serum sample bank was applied, and PSA was assessed.

Results: The estimated sensitivity of the test was 44% and specificity 94% at a cutoff of 4.0 microg./l. in the total material. The sensitivity had improved to 86% in patients diagnosed in 5 years after the sample drawing. The test had a better sensitivity (93%) and specificity (96%) in men younger than 65 years at the time of the sample drawing compared to those older. The sensitivity further improved to 100% with a cutoff of 2.5 microg./l.

Conclusions: PSA is a valid screening test for prostate cancer, which compares favorably with mammography for breast cancer. However, until an effect on mortality has been shown, routine screening cannot be recommended.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Blood Banks
  • Finland
  • Follow-Up Studies
  • Humans
  • Male
  • Mass Screening*
  • Middle Aged
  • Prostate-Specific Antigen / blood*
  • Prostatic Neoplasms / blood*
  • Prostatic Neoplasms / diagnosis*
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Prostate-Specific Antigen