96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...
96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...
96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...
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Kolorektales Karzinom 2<br />
VO-005<br />
Translating biology of colorectal cancer into clinical applications<br />
G .A . Meijer 1<br />
1VU University Medical Center, VU University Medical Center, Amsterdam,<br />
Netherlands<br />
Colorectal cancer (CRC) is one of the most common malignancies and<br />
represents a substantial burden for society, in terms of patient suffering<br />
as well as economically. As cancer is an evolutionary process in which<br />
genotype drives phenotype, knowledge of the biological mechanisms<br />
un<strong>der</strong>lying CRC can help to improve patient outcome. Translational research<br />
in CRC mainly focuses on unmet clinical needs in three stages of<br />
the disease, i.e. early detection or screening, prognostication in primary<br />
CRC and prediction of response to drug therapy in metastatic CRC.<br />
As CRC develops over a number of years from a detectable precursor<br />
(adenoma), there is a window of opportunity for early detection and curative<br />
intervention. Our increased un<strong>der</strong>standing of CRC biology, and in<br />
particular adenoma to carcinoma progression, has yielded a number of<br />
markers based on e.g. DNA or proteins that hold great promise for the<br />
next generation CRC screening tests.<br />
In primary CRC, standard UICC staging is still the most important<br />
method for stratifying patients by risk of recurrence. Yet, the substantial<br />
number of stage II patients that do develop recurrences, and the still<br />
small proportion of stage III patients that actually benefit from adjuvant<br />
therapy, un<strong>der</strong>line the need for additional diagnostic arsenal. Since CRC<br />
biologically is a heterogeneous disease, it does not come as a surprise<br />
that there is a large number of markers for which some level of evidence<br />
exists that they could have additional prognostic value. The main challenge<br />
here is to make the next step to get these markers validated and<br />
implemented in routine diagnostic practice.<br />
In a similar way, much translational research has successfully translated<br />
biology of CRC into diagnostic tests that more rapidly have been implemented,<br />
like KRAS testing for anti-EGFR therapy. The fact that these<br />
predictive markers have entered the field much more rapidly than the<br />
prognostic markers most likely is associated with more efficient business<br />
development, stimulated by the companion diagnostic concept. Yet, also<br />
here challenges remain, as because of the complexity of CRC biology it<br />
is much more likely that we will have complex decision trees rather than<br />
single parameter tests to stratify patients for drug therapy. The exciting<br />
developments that will bring whole cancer genome sequencing within<br />
the reach of pathologists will eliminate current barriers for the full exploration<br />
of tumor biology for the purpose of diagnostic pathology.<br />
Keynote Lecture<br />
VO-007<br />
Deep Sequencing - new frontiers in GI-tumor pathology<br />
N . Papadopoulos<br />
Johns Hopkins University, Baltimore, USA<br />
Inflammatory bowel diseases represent a chronic disor<strong>der</strong> accompanying<br />
mostly young people throughout their life. Thus therapeutic strategies<br />
allowing for a normal life are mandatory. Although the incidence is<br />
increasing and the research of the last decades provides a detailed view<br />
of the pathogenesis, the available therapeutic strategies are still symptomatic.<br />
The primary aim is to induce a stable remission. Depending on<br />
disease localization as well as associated complications such as fistulas,<br />
abscesses and malnutrition, the therapeutic strategies range from local<br />
applications up to systemic immunosuppressive medications. Despite<br />
the availability of highly potent agents including azathioprine, calci-<br />
neurin inhibitors as well as anti-TNF antibodies, there is still a subset<br />
of patients that remains with active disease. Thus it is crucial to predict<br />
the disease course early on, in or<strong>der</strong> to decide whether early aggressive<br />
therapy is required or a less aggressive treatment is sufficient. Some factors<br />
helping with this decision have already been identified. Novel data<br />
suggest that the expression profile of CD8+ cells may help in predicting<br />
the disease course. However, these data will have to be confirmed in<br />
prospective studies. Equally important is the question when immunosuppressive<br />
therapies can be paused with low risk. Do we need clinical,<br />
endoscopic or even histological remission? On a long-term view mucosal<br />
healing gains impact since it reduces the risk of developing colorectal<br />
cancer. The discussed points emphasize that therapeutic strategies in<br />
inflammatory bowel diseases represent an increasingly individualized<br />
therapy in or<strong>der</strong> to allow for a high life quality of our patients.<br />
Primäre Entzündungen im GI-Trakt<br />
VO-008<br />
Clinical view and novel therapeutic strategies in inflammatory<br />
bowel diseases<br />
B . Siegmund1 1Charité – Universitätsmedizin Berlin, Klinik <strong>für</strong> Gastroenterologie, Infektiologie<br />
und Rheumatologie <strong>der</strong> Charite Campus Benjamin Franklin, Berlin<br />
Inflammatory bowel diseases represent a chronic disor<strong>der</strong> accompanying<br />
mostly young people throughout their life. Thus therapeutic strategies<br />
allowing for a normal life are mandatory. Although the incidence is<br />
increasing and the research of the last decades provides a detailed view<br />
of the pathogenesis, the available therapeutic strategies are still symptomatic.<br />
The primary aim is to induce a stable remission. Depending on<br />
disease localization as well as associated complications such as fistulas,<br />
abscesses and malnutrition, the therapeutic strategies range from local<br />
applications up to systemic immunosuppressive medications. Despite<br />
the availability of highly potent agents including azathioprine, calcineurin<br />
inhibitors as well as anti-TNF antibodies, there is still a subset<br />
of patients that remains with active disease. Thus it is crucial to predict<br />
the disease course early on, in or<strong>der</strong> to decide whether early aggressive<br />
therapy is required or a less aggressive treatment is sufficient. Some factors<br />
helping with this decision have already been identified. Novel data<br />
suggest that the expression profile of CD8+ cells may help in predicting<br />
the disease course. However, these data will have to be confirmed in<br />
prospective studies. Equally important is the question when immunosuppressive<br />
therapies can be paused with low risk. Do we need clinical,<br />
endoscopic or even histological remission? On a long-term view mucosal<br />
healing gains impact since it reduces the risk of developing colorectal<br />
cancer. The discussed points emphasize that therapeutic strategies in<br />
inflammatory bowel diseases represent an increasingly individualized<br />
therapy in or<strong>der</strong> to allow for a high life quality of our patients.<br />
VO-010<br />
Microscopic colitis: clinical appearance and therapy<br />
S . Miehlke1 1Magen-Darm-Zentrum, Hamburg<br />
Microscopic colitis (MC) is a chronic inflammatory bowel disease which<br />
is increasingly recognized as a common cause of chronic, non-bloody<br />
diarrhoea. Besides watery diarrhea, many patients also suffer from abdominal<br />
pain, weight loss and fecal incontinence which severely deteriorate<br />
their quality of life. There is a female predominance with an average<br />
age at diagnosis around 60 years. Smoking appears to be a relevant risk<br />
factor. Epidemiological studies have shown a rising incidence in the last<br />
Der Pathologe · Supplement 1 · 2012 |<br />
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