Objectives. To evaluate pathologic characteristics and biochemical survival
rate differences between patients with Gleason score 6 or less, 7, and 8 o
r more prostate cancer.
Methods. A total of 652 patients who underwent a radical prostatectomy for
clinically localized prostate cancer between March 1991 and December 1995 w
ere selected for this study. Patients who underwent neoadjuvant or adjuvant
hormonal therapy or radiotherapy were excluded. Clinical and pathologic da
ta were obtained from our prostate cancer data base. Serum prostate-specifi
c antigen (PSA) level, pathologic stage, and disease-free survival (DFS) we
re analyzed between the three Gleason score groups.
Results. The overall mean pretreatment serum PSA level was 12.9 ng/mL, bein
g 8.4, 13.4, and 23 ng/mL for Gleason score 6 or less, 7, and 8 or more pro
state cancers, respectively (P = 0.0001). Of patients with specimen Gleason
score 6 or less, 7, and 8 or more, pathologic organ-confined disease was p
resent in 69.4%, 43.1%, and 9.2%, respectively (P = 0.001). Extraprostatic
extension was present in 30.6%, 56.9%, and 90.8% (P = 0.0001); positive sur
gical margins, considered independently from the other pathologic findings,
were present in 31%, 47.6%, and 67.8% of patients with Gleason score 6 or
less, 7, and 8 or more, respectively (P = 0.0001). DFS was 34.5% for patien
ts with Gleason score 8 or more, 75% for Gleason score 7, and 91.2% for Gle
ason score 6 or less prostate cancers, at a median follow-up of 34.2 months
(P = 0.0001). On multivariable analysis, after adjusting for serum PSA lev
el (10 or less or more than 10 ng/mL) and pathologic stage, Gleason score (
6 or less, 7, 8 or more) remained a statistically significant predictor of
DFS (P = 0.0001).
Conclusions. Patients with Gleason score 7 prostate cancer should be consid
ered a specific prognostic category. We believe that this distinction is cr
itical to obtain more reliable results from prostate cancer analyses about
prognosis of patients treated with curative intent. (C) 1999, Elsevier Scie
nce Inc. All rights reserved.