A new era of PSA testing has been ushered in by identifying and measur
ing various molecular forms of PSA in the serum. The introduction of t
hese concepts into clinical medicine makes it possible for us to ident
ify the carcinoma of the prostate at an early and curable state and to
avoid negative and expensive biopsies of the prostate. The present st
ate of data shows that percentage-free PSA and not percentage-bound PS
A is the better discriminator within the total PSA range between 2.5-3
.0 and 10.0 ng/ml to differentiate patients with an early-stage carcin
oma of the prostate against those with benign prostate hypertrophy. In
this range of data percentage-free PSA improved the clinical performa
nce of the PSA test by 20-25%. If the total PSA value is normal (< 4.0
ng/ml), percentage-free PSA yields better sensitivity and, if the tot
al PSA value is slightly elevated (4.1-10 ng/ml), percentage-free PSA
improves specificity. Both aspects are highly desirable in View of the
aim to detect an organ-located carcinoma of the prostate early and co
st-effectively within a group of patients with a high prevalence of be
nign prostate hypertrophy (BPH).