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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 />

7

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