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96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...

96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...

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Abstracts<br />

SA-P-081<br />

Significance of Gleason Grading in a clinical setting that consi<strong>der</strong>s<br />

active surveillance as a therapeutic option of prostatic low grade<br />

cancer<br />

B . Helpap 1 , G . Kristiansen 2 , J . Köllermann 3 , U . Oehler 1 , C . Fellbaum 1<br />

1 HBH-Hospital, Dept . Pathology, Singen, 2 University of Bonn, Dept . Pathology,<br />

Bonn, 3 HKS-Wiesbaden, Dept . Pathology, Wiesbaden<br />

Aims. Active surveillance has become an increasingly accepted clinical<br />

strategy to handle patients with presumably insignificant carcinomas<br />

by observant waiting, without endangering the curative intent. Aim of<br />

this analysis was to evaluate the diagnostic value of nuclear features in<br />

addition to Gleason grade in the prediction of non-aggressive disease in<br />

a large and representative prostate cancer cohort.<br />

Methods. A cohort of 968 prostatectomy specimens with matching preceding<br />

biopsies (12 cores) was morphologically analysed. Architectural<br />

features according to Gleason and cytological grading were recorded<br />

and compared.<br />

Results. The combination of architectural and cytoplogical features as<br />

incorporated in the Helpap Grading increase the rate of agreement of<br />

grading between the biopsy and the prostatectomy specimens especially<br />

GS 6 up to 90%. The parallel use of Gleason and Helpap grading allows<br />

for a better prediction of organ confined disease (pT2) following prostatectomy.<br />

Conclusions. By adding cytologic features to Gleason grading, an increased<br />

diagnostic accuracy in the identification of low grade carcinomas,<br />

which may be treated by active surveillance, can be achieved.<br />

SA-P-082<br />

The Microtubule-associated Protein 2 (MAP2) is frequently expressed<br />

in prostate cancer and its precursor lesions<br />

M . Majores1 , E . Krappe1 , N . Wernert1 , J . Ellinger2 , G . Kristiansen1 1 2 University of Bonn, Department of Pathology, Bonn, University of Bonn,<br />

Department of Urology, Bonn<br />

Aims. The microtubule-associated protein 2 (MAP2) is involved in microtubule<br />

assembly and plays a crucial role for nucleation and stabilization<br />

of microtubules. MAP2 is frequently expressed in mature neurons<br />

and tissue with neuroendocrine differentiation.<br />

Methods. We incidentally revealed that MAP2 is expressed in prostate<br />

cancer (PCA) and have evaluated the immunohistochemical characteristics<br />

of MAP2 expression in 107 PCA specimens in comparison to adjacent<br />

normal and dysplastic tissue.<br />

Results. MAP2 expression was strikingly focused on high-grade PIN lesions<br />

and invasive tumour glands: mo<strong>der</strong>ate or strong immunolabelling<br />

was found in 92% of high-grade PIN (n=61/68) and in 58% (n=62/107) of<br />

low-grade PIN lesions. In contrast, normal glands or hyperplastic epithelia<br />

of the periurethral zone stained weakly. Invasive carcinoma was<br />

MAP2-positive in 86% of Gleason pattern (GP) 3 glands (n=89/103), in<br />

78% of GP 4 (n=28/36) and in 75% of GP 5 areas (n=6/8). In several cases,<br />

MAP2 was expressed in high-grade PINs with continuous transition to<br />

invasive carcinomas.<br />

Conclusions. Our preliminary findings support MAP2 as a promising<br />

new immunomarker for PCA and PIN lesions and moreover point to<br />

MAP2 as an “interface marker” in the progression from in-situ lesions to<br />

invasive carcinomas. We currently conduct correlations between MAP2<br />

expression and clinicopathological features including patient survival<br />

times.<br />

164 | Der Pathologe · Supplement 1 · 2012<br />

SA-P-083<br />

CyclinD1 expression indicates possible lymph node metastasis in<br />

invasive blad<strong>der</strong> cancer<br />

J . Rokahr1 , E . Herrmann2 , M . Bögemann2 , S . Bierer2 , E . Eltze3 1 2 University of Muenster, Institute of Pathology, University of Muenster,<br />

Department of Urology, 3Institute of Pathology Saarbrücken Rastpfuhl,<br />

Saarbrücken<br />

Aims. Overexpression of proteins involved in antiapoptosis or proliferation<br />

is often associated with tumour progression and treatment resistance.<br />

Cyclin D1 and BCL2 play a potential role in progression of blad<strong>der</strong> cancer<br />

like Ki67 and TP53.<br />

Methods. Immunhistochemical stainings were performed for Cyclin D1,<br />

BCL2, TP53 and Ki67 on TMA containing paraffin embedded tissues of<br />

219 invasive blad<strong>der</strong> cancer patients who had un<strong>der</strong>gone radical cystectomy<br />

between 1987 and 2004. The results were correlated with clinicopathological<br />

parameters and overall and recurrence-free survival.<br />

Results. Expression of the BCL2 was found in only 19 tumours, and only<br />

mo<strong>der</strong>ately in 6 of these. Overexpression of BCL2 correlated with a low<br />

proliferation rate (Ki67< 10%, p=0.067) and a low grade (p=0.004). No<br />

correlation could be found to pTstage or TP53 expression or survival<br />

data. Cyclin D1 expression of correlated significantly with pN1 (p=0.031),<br />

whereas no correlations to tumour stage, grade, TP53 expression or proliferation<br />

rate could be detected. Kaplan Meier analysis showed a significant<br />

shorter overall survival for patients with Cyclin D1 expression<br />

tumours (p=0.022).<br />

Conclusions. The correlation between Cyclin D1 expression and lymph<br />

node metastasis and a poor prognosis in invasive blad<strong>der</strong> cancer after<br />

cystectomy indicates a role in mediating invasion and metastasis of cancer<br />

cells.<br />

SA-P-084<br />

High IMP3 protein expression is a negative prognostic factor in<br />

advanced urothelial carcinoma of the blad<strong>der</strong><br />

H . Reis1 , 2 , F . vom Dorp3 , C . Niedworok3 , C . Niedworok4 , A . Melchior-Becker4 ,<br />

J .W . Fischer4 , D . Gödde1 , B .B . Singer5 , A . Bankfalvi2 , I . Romics6 , K .W . Schmid2 ,<br />

S . Störkel1 , S . Ergün5 , H . Rübben3 , T . Szarvas3 , 7<br />

1 2 University of Witten/Herdecke, Institute of Pathology, Wuppertal, University<br />

of Duisburg-Essen, Institute of Pathology and Neuropathology, Essen,<br />

3 4 University of Duisburg-Essen, Department of Urology, Essen, University<br />

of Duisburg-Essen, Institute of Pharmacology and Clinical Pharmacology,<br />

Essen, 5University of Duisburg-Essen, Institute of Anatomy, Essen, 6Semmel weis University Budapest, Department of Urology, Budapest, Hungary,<br />

7Medical University of Vienna, Department of Urology, Wien, Austria<br />

Aims. The identification of the prognostic influence and interactions of<br />

the Insulin-like growth factor mRNA-binding protein 3 (IMP3) in advanced<br />

urothelial carcinoma of the blad<strong>der</strong> (UCB).<br />

Methods. A total of 224 urothelial blad<strong>der</strong> carcinoma cases were studied<br />

regarding IMP3 expression by immunohistochemistry, real-time PCR<br />

and Western blot analyses. The molecular targets of IMP3 – CD44, IGF2<br />

and its receptor IGF1-R – were also investigated. Expression levels were<br />

correlated with clinical follow-up data in univariate and multivariate<br />

analyses.<br />

Results. In high-stage and high-grade UCB both IMP3 protein and<br />

mRNA levels were significantly elevated. In muscle-invasive cancer<br />

IMP3 protein but not gene expression proved to be an independent<br />

predictor of disease-specific (HR=2.58, 95%CI 1.28–4.56, p=0.004) and<br />

overall survival (HR=2.07, 95%CI 1.12–3.82, p=0.020). IGF2 and CD44<br />

expression showed no correlation with that of IMP3.<br />

Conclusions. Identification of high IMP3 protein levels in UCB might aid<br />

in the selection of patients at high risk for disease progression and in the<br />

stratification to groups with more intensive therapy or strict follow-up.<br />

No tumor promoting effect of IMP3 in its regulatory action on IGF2 and<br />

CD44 expression was observable.

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