Potentially advanced malignancies detected by screening for prostate carcinoma after an interval of 4 years

Cancer. 2004 Mar 1;100(5):968-75. doi: 10.1002/cncr.20048.

Abstract

Background: At the Rotterdam branch of the European Randomized Study of Screening for Prostate Cancer, a cohort of 19,970 men ages 55-75 years is screened at an interval of 4 years. Screening includes systematic sextant needle biopsy for men with elevated prostate-specific antigen (PSA) levels and/or positive findings on digital rectal examination or transrectal ultrasound. Detection during the second screening round of a large number of high-grade (Gleason Grade 4 or 5) malignancies and/or a large number of malignancies in general could be considered the result of a failure to identify these malignancies at an early stage, during prevalence screening.

Methods: Men diagnosed during the second screening round with potentially advanced carcinoma (PAC), characterized by a biopsy Gleason score of 7 (4 + 3, or 3 + 4 with > 30% malignant involvement) or a biopsy Gleason score of 8-10, were identified. Clinical data, including PSA values on prevalence screening, biopsy history, clinical stage, and follow-up data, were retrieved for these patients. Tumor features were further analyzed in radical prostatectomy specimens.

Results: During the second screening round, 503 malignancies, including 30 (6.0%) with features of PAC on diagnostic biopsy, were detected in 11,210 patients. Curative treatment was offered to 26 patients. Prostatectomy demonstrated the presence of organ-confined disease in 11 of 12 specimens, and tumor volume ranged from 0.11-7.93 cm3 (median, 1.05 cm3). PSA failure was noted in 6 of 22 patients who were offered curative therapy.

Conclusions: PAC is a rare finding in the second round of screening after a 4-year interval, and a substantial proportion of PAC cases detected in the second screening round represent organ-confined disease. The findings of the current study suggest that the screening protocol used is sufficiently effective for detecting > 95% of malignancies before they develop features that would make them incurable.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Age Distribution
  • Aged
  • Androgen Antagonists / therapeutic use
  • Biopsy, Needle
  • Carcinoma / epidemiology
  • Carcinoma / pathology*
  • Carcinoma / therapy
  • Humans
  • Immunohistochemistry
  • Incidence
  • Male
  • Mass Screening / methods*
  • Middle Aged
  • Neoplasm Staging
  • Netherlands
  • Prognosis
  • Prostate-Specific Antigen / analysis*
  • Prostatectomy
  • Prostatic Neoplasms / epidemiology
  • Prostatic Neoplasms / pathology*
  • Prostatic Neoplasms / therapy
  • Radiotherapy / methods
  • Risk Assessment
  • Sensitivity and Specificity
  • Survival Rate
  • Time Factors

Substances

  • Androgen Antagonists
  • Prostate-Specific Antigen