Objectives. Stage T1 c carcinoma of the prostate is defined as a nonpa
lpable carcinoma (NPC-P) that is not visible by imaging and is identif
ied by needle biopsy performed because of elevated prostate-specific a
ntigen (PSA) concentrations. The purpose of this study was to define t
he incidence of normal findings on transrectal ultrasound (TRUS) and/o
r endorectal coil magnetic resonance imaging (EMRI) among patients wit
h NPC-P, as well as to investigate the value of differentiating patien
ts with Stage Tie disease from all other patients with NPC-P. Methods.
The records of 2211 patients diagnosed with prostate carcinoma betwee
n 1988 and 1995 were reviewed to identify 291 men with NPC-P. TRUS and
EMRI reports were analyzed with regard to the presence and laterality
of hypoechoic nodules or low-signal areas reported on T2-weighted ima
ges, respectively, Ninety percent of patients (n = 262) had at least s
ix prostate biopsies, 185 patients (64%) underwent both TRUS and EMRI,
224 (77%) had TRUS, and 251 (86%) had an EMRI study. Results. Results
were considered normal in 101 (47%) of 214 patients undergoing TRUS,
in 58 (23%) of 249 undergoing EMRI, and in 22 (12%) of 185 undergoing
both TRUS and EMRI. For the side of the prostate with positive biopsy
results, correlation with imaging abnormalities was better for EMRI th
an for TRUS (39% versus 24%). There was no significant difference in m
ean PSA value, distribution of Gleason score, or unilateral versus bil
ateral positive biopsy results among patients with normal versus abnor
mal findings on both TRUS and EMRI. Conclusions. (1) Only 12% of men w
ith NFC-P have no TRUS or EMRI abnormalities, fulfilling the criteria
for Stage Tie prostate carcinoma. (2) Those patients with Stage Tie di
sease do not differ from patients with NPC-P up-staged by TRUS or EMRI
, with regard to pretreatment PSA levels, Gleason scores, and the prob
ability of having bilateral rather than unilateral positive biopsy res
ults. (3) The value of classifying patients with NPC-P into Stage Tie
versus higher stages of prostate carcinoma on the basis of imaging sho
uld be questioned. (C) 1997, Elsevier Science Inc. All rights reserved
.