PROSTATE VOLUME AND CANCER IN SCREENING PROGRAMS

Citation
B. Standaert et al., PROSTATE VOLUME AND CANCER IN SCREENING PROGRAMS, The Prostate, 33(3), 1997, pp. 188-194
Citations number
29
Categorie Soggetti
Endocrynology & Metabolism","Urology & Nephrology
Journal title
ISSN journal
02704137
Volume
33
Issue
3
Year of publication
1997
Pages
188 - 194
Database
ISI
SICI code
0270-4137(1997)33:3<188:PVACIS>2.0.ZU;2-L
Abstract
BACKGROUND. Prostate cancer screening is studied in a randomized trial in Antwerp, Belgium. The case group receives three screening tests (D RE, TRUS, and PSA). Intermediate evaluation shows that only 1/3 of the biopsy results is positive (35/125). The proposed analysis identifies variables that determine the biopsy outcome. METHODS. Multiple logist ic regression analysis is used to regress biopsy results (n = 125) by age (60-74), PSA, PSA-D, prostate volume, TRUS, and DRE. Continuous va riables are transformed into quartile values. Robustness of the outcom e is tested with ROC and sensitivity analysis on age. RESULTS. Biopsy outcomes are best explained (82.3%) by PSA, DRE, and DRE related to vo lume. Volume is more sensitive than age to explain the biopsy result. PSA-D, instead of PSA, does not procure more precise information when a high PSA cut-off level is used. Restricting the analysis to the 60-7 0-year-old age group shows that volume is more sensitive. ROC-analysis confirms the findings. CONCLUSIONS. When performing prostate cancer m ultitest screening among a wide age range, the use of uniform screenin g criteria is difficult to accept due to differences in prostate volum e. Logistic regression analysis is an appropriate method to identify c ut-off levels for prostate volume. (C) 1997 Wiley-Liss, Inc.