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EAU 2013 - Programme Book - YouMed

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Sunday<br />

Sunday, 17 March - <strong>EAU</strong> <strong>Programme</strong><br />

164 <strong>Programme</strong> <strong>Book</strong><br />

Thematic Session 3<br />

11.00 - 12.00 From bench to bedside: What will be replacing PSA?<br />

Blue Hall 1-2 - Level N1<br />

Chair: Z. Culig, Innsbruck (AT)<br />

11.00 - 11.15 State-of-the-art lecture Gene fusions in prostate cancer: Is it helping?<br />

T. Visakorpi, Tampere (FI)<br />

Aims and objectives<br />

The finding of TMPRSS2:ERG fusion immediately raised the question could it be utilized in the treatment of<br />

prostate cancer, either as a drug target or as a biomarker. What is good about the fusion genes as biomarkers,<br />

is that they are genetic alterations. As such they are cancer specific and do not exist in normal cells. There<br />

has been a large number of publications interrogating whether the TMPRSS2:ERG fusion detected in tissue<br />

specimen is associated with prognosis. Most of the studies suggest it is not. There have also been a few<br />

studies detecting the fusion from blood, circulating tumor cells (CTCs), and urine. And, it seems that in a<br />

combination with PCA3, TMPRSS2:ERG could improve the utility of serum PSA to detect clinically significant<br />

cancer. Also other fusion genes than TMPRSS2:ERG have been and will be identified in prostate cancer.<br />

Common factor for these fusions is that they are rare. Thus, they will unlikely have a potential of being<br />

biomarkers alone. However, they may turn out to be useful in selecting targeted drugs if available.<br />

11.15 - 11.30 State-of-the-art lecture The role of the pathologist in clinical prognosis<br />

G. Kristiansen, Bonn (DE)<br />

11.30 - 11.45 State-of-the-art lecture MicroRNA in prostate cancer diagnosis<br />

H. Sültmann, Heidelberg (DE)<br />

Aims and objectives<br />

miRNAs are small non-coding RNAs involved in posttranscriptional regulation of gene expression. While<br />

recent studies have suggested the usefulness of miRNAs in tissues and body fluids for tumor diagnosis,<br />

prognosis, and prediction, technical parameters, e.g. nucleic acid recovery from limited sources of<br />

biomaterial, sample standardisation, data normalisation, as well as independent validation of screening<br />

data, are still challenging. The presentation will highlight the potential as well as obstacles for translating<br />

miRNA markers into diagnostic applications for prostate cancer.<br />

11.45 - 12.00 Abstract presentations: Special selection from the poster sessions<br />

1045 Urinary PCA3 and TMPRSS2:ERG help predict biopsy outcome prior to initial prostate biopsy using a risk<br />

group analysis<br />

J.R. Day, L.A. Jones, S.E. Meyer, P.N. Hodge, J. Aussie, D.R. Saltzstein, J.C. Groskopf (San Diego, San Antonio,<br />

United States of America)<br />

139 Reducing unnecessary biopsies for suspicion of prostate cancer: Extension and validation of an ERSPC<br />

based risk calculator with Phi<br />

M.J. Roobol, D. Nieboer, A. Houlgatte, S. Vincendeau, M. Lazzeri, G. Guazzoni, C. Stephan, A. Semjonow,<br />

A. Haese, M. Graefen, E.W. Steyerberg (Rotterdam, The Netherlands; Paris, Rennes, France; Milan, Italy;<br />

Berlin, Munster, Hamburg, Germany)

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