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PATHOLOGY
doi: 10.1590/S1677-553820100002000021
Radical
prostatectomy (RP) findings in cases with only intraductal carcinoma of
the prostate (IDC-P) on needle biopsy
Robinson BD, Epstein JI
Dep. of Pathology, The Johns Hopkins Hospital, Baltimore, MD, USA
Mod Pathol 2010; 23 (suppl 1): 215A
- Background:
When IDC-P is present on biopsy, it is usually seen with infiltrating
acinar adenocarcinoma. In 2006, we reported 27 cases with IDC-P only
on biopsy; however, only 6 cases had available RP findings.
Design: 82 men with IDC-P only on prostate biopsy were identified from
the consult files of one of the authors. Follow-up information was available
in 66 cases. 20 men were treated with RP, 17 radiation therapy (RT),
8 hormone therapy (HT), 13 RT and HT, 6 active surveillance, and 2 rebiopsy.
An attempt was made to retrieve the slides of all 20 RP cases.
Results: Of the 20 RP cases, 5 showed extraprostatic extension, 3 seminal
vesicle invasion, 10 were organ-confined, and 2 showed extensive IDC-P
only without identifiable invasive cancer. Of the 18 cases with invasive
cancer, the average Gleason score (GS) was 7.8. 1 patient developed
bone metastases 3 years post-RP, and 3 others were post-RP PSA failures.
13 RPs were available for our review. 9 showed extensive IDC-P (including
one case of IDC-P only), defined as > 10% of the tumor volume being
intraductal; 3 focal IDC-P; and 1 no IDC-P. All cases with invasive
carcinoma were acinar, although 3 cases were classified as ductal by
referring pathologists. We concurred with the outside GS in 5/13 cases
(5 undergraded, 3 overgraded). In the 3 cases that we gave lower GS,
the outside institution graded cribiform IDC-P with and without necrosis
as Gleason pattern 5 or 4, respectively.
Conclusions: Our study, the largest to date with RP findings following
IDC-P only on needle biopsy, confirms that aggressive therapy is appropriate
for patients whose biopsies show only IDC-P. It is likely that the pathological
findings are even worse than we report herein, as most RPs were only
partially sampled. Most cases likely represent intraductal spread of
high grade cancer, but some cases represent in situ acinar adenocarcinoma.
- Editorial
Comment
Intraductal carcinoma of the prostate (IDC-P) is defined as presence
of atypical cells that span the entire lumen of prostatic ducts or acini
while the normal architecture of ducts or acini is still maintained
including presence of basal cells (1,2). With presence of IDC-P on a
biopsy, the pathologist considers 4 possibilities: 1) ductal carcinoma;
2) high-grade intraepithelial neoplasia (HGPIN); 3) intraductal carcinoma;
and, 4) intraductal spread of an invasive carcinoma.
Ductal carcinoma may be ruled out because of the presence of basal cells;
in cases of irregularity and distortion of the ducts, HGPIN may also
be ruled out; and, in presence of an invasive carcinoma, intraductal
spread is most probable and the finding adds no additional information
to the report. The problem is related to cases that IDC-P is the only
finding on a biopsy.
The Johns Hopkins group studied 20 radical prostatectomy specimens of
patients who presented on biopsy only the diagnosis of IDC-P. Two out
of twenty patients showed extensive IDC-P only, without identifiable
invasive cancer. IDC-P in these 2 patients may represent: 1. an early
phase of ductal or acinar carcinoma; or 2. intraductal spread of an
invasive not detected tumor.
According to the authors, IDC-P as the only finding on needle biopsy
corresponds to almost always to aggressive tumors and the patients may
have definitive treatment. A more conservative approach would be an
extended rebiopsy in order to detect a possible invasive cancer.
References
1. Cohen RJ, McNeal JE, Baillie T: Patterns of differentiation and
proliferation in intraductal carcinoma of the prostate: significance
for cancer progression. Prostate. 2000; 43: 11-9.
2. Guo CC, Epstein JI: Intraductal carcinoma of the prostate on needle
biopsy: Histologic features and clinical significance. Mod Pathol.
2006; 19: 1528-35.
Dr.
Athanase Billis
Full-Professor of Pathology
State University of Campinas, Unicamp
Campinas, São Paulo, Brazil
E-mail: athanase@fcm.unicamp.br
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