Gleason grade, especially at low and high ends of the spectrum, is a k
nown predictor of pathologic stage. What are needed are predictors of
stage with Gleason sum 5 to 7 tumors, which encompasses the majority o
f clinically organ-confined tumors, In this study, we analyzed whether
cell proliferation and apoptosis (programmed cell death) were correla
ted with stage in men with clinically organ-confined Gleason sum 6 to
7 cancer, We studied 98 radical prostatectomies with the following pat
hologic stages: organ-confined disease (n = 28); capsular penetration
(n = 28); seminal vesicle invasion (n = 21); and pelvic lymph node met
astases (n = 21), Histological sections from the radical prostatectomi
es were stained for cell proliferation using MIB1 antibody (Ki-67) and
for apoptosis using the TUNEL technique. The extent of staining was r
ecorded as the number of positive cells per 1000 cells, Overall daily
growth (kp) was calculated as: kp = (ki/2) (apoptosis/0.5), based on t
he time of prostate cancer to undergo mitosis and apoptosis per day, U
sing logistic regression analysis, pathologic stage did not correlate
with cell proliferation, apoptosis, or overall daily growth, These par
ameters also did not distinguish between Gleason sum 6 and Gleason sum
7 tumors, We supplemented these cases with examples of Gleason sum le
ss than or equal to 4 and Gleason sum greater than or equal to 8 to st
udy cell proliferation and cell death in the full spectrum of Gleason
grades, There was a significant difference (P = 0.005) in cell prolife
ration between Gleason sum greater than or equal to 6 and Gleason sum
less than or equal to 4 tumors, but apoptosis and daily growth were no
t significant, We conclude that cell proliferation and apoptosis do no
t correlate with pathological stage in clinically organ-confined cance
r with Gleason sum 6 or 7, but that cell proliferation can distinguish
between high (Gleason sum greater than or equal to 6) and low (Gleaso
n sum less than or equal to 4) grade tumors.