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Report in English with a Dutch summary (KCE reports 45A)

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<strong>KCE</strong> <strong>reports</strong> vol.45 Screen<strong>in</strong>g for Colorectal Cancer: Appendices 157<br />

9 CONCLUSIONS AND RECOMMENDATIONS<br />

The purpose of this HTA on Colorectal Cancer (CRC) Screen<strong>in</strong>g was to<br />

evaluate whether, and under which conditions, CRC screen<strong>in</strong>g could become an<br />

effective and cost-effective method to reduce the burden of CRC <strong>in</strong> Belgium.<br />

Therefore, we analysed and evaluated the available evidence about CRC<br />

screen<strong>in</strong>g. We also evaluated the uncerta<strong>in</strong>ties surround<strong>in</strong>g CRC screen<strong>in</strong>g and<br />

identified areas where specific additional data are necessary before such a<br />

program can successfully be implemented <strong>in</strong> this country.<br />

9.1 CONCLUSIONS<br />

Provided that the organisational conditions are met, colorectal cancer screen<strong>in</strong>g<br />

clearly fulfils the orig<strong>in</strong>al Wilson and Jung criteria and also the more recent<br />

extended criteria regard<strong>in</strong>g practical and ethical issues. These extensions of the<br />

criteria ma<strong>in</strong>ly emphasize that screen<strong>in</strong>g programs should be concerted actions,<br />

<strong>with</strong> adequate quality assurance, broadly accessible and <strong>with</strong> full <strong>in</strong>formation<br />

about potential benefits and harms but <strong>with</strong>out any moral pressure on<br />

<strong>in</strong>dividuals to participate. In the case of CRC screen<strong>in</strong>g we observed that <strong>in</strong><br />

most countries opportunistic screen<strong>in</strong>g, historically, is the ma<strong>in</strong> form of<br />

screen<strong>in</strong>g. Recently, however, several countries started pilot projects to f<strong>in</strong>d<br />

out how to organise a programmed mass screen<strong>in</strong>g for CRC.<br />

In Belgium, colorectal cancer is the third most common cancer <strong>in</strong> men and the<br />

second most common cancer <strong>in</strong> women. It is also the second most common<br />

cause of cancer death. Its <strong>in</strong>cidence rises <strong>with</strong> age and every year CRC is<br />

diagnosed <strong>in</strong> approximately 7700 Belgians. Even though men have, at every age,<br />

a higher <strong>in</strong>cidence of CRC, the absolute number of CRC <strong>in</strong> women is also high<br />

because of their longer life expectancy. Survival after the diagnosis of CRC is<br />

strongly associated <strong>with</strong> stage of disease at diagnosis: the more localised the<br />

tumor, the better the prognosis. Therefore, early identification of the<br />

malignancy through screen<strong>in</strong>g is considered important.<br />

Most CRC occur sporadically, i.e. <strong>in</strong> <strong>in</strong>dividuals <strong>with</strong>out apparent evidence of<br />

<strong>in</strong>creased risk. However, about 25 to 30% of CRC occur <strong>in</strong> <strong>in</strong>dividuals who are<br />

known to be at <strong>in</strong>creased risk, either through a family history of CRC<br />

occurrence or through personal predispos<strong>in</strong>g conditions. Although to date no<br />

exact numbers are available for Belgium, it can be estimated that this population<br />

amounts to about 15% of the general population, assum<strong>in</strong>g an average twofold<br />

risk <strong>in</strong> this subpopulation as a whole. Those <strong>in</strong>dividuals should not be the target<br />

of mass screen<strong>in</strong>g programs but nevertheless should be cared for. Therefore,<br />

we <strong>in</strong>cluded <strong>in</strong> this report reviews of general recommendations for risk<br />

stratification for CRC and of guidel<strong>in</strong>es for tak<strong>in</strong>g care of <strong>in</strong>dividuals at<br />

<strong>in</strong>creased or at high risk. Those <strong>in</strong>dividuals should be referred to appropriate<br />

regular healthcare.<br />

Many guidel<strong>in</strong>es on CRC screen<strong>in</strong>g and surveillance are available worldwide,<br />

<strong>in</strong>clud<strong>in</strong>g the position paper on cancer screen<strong>in</strong>g <strong>in</strong> the European Union, and we<br />

described many of those. All guidel<strong>in</strong>es recommend CRC screen<strong>in</strong>g to be<br />

offered to low risk patients start<strong>in</strong>g at age 50, and all guidel<strong>in</strong>es also<br />

recommend us<strong>in</strong>g colonoscopy for the follow-up of <strong>in</strong>dividuals <strong>with</strong> a positive<br />

screen<strong>in</strong>g test. However, guidel<strong>in</strong>es disagree on optimal age span of screen<strong>in</strong>g<br />

and on optimal screen<strong>in</strong>g techniques. If FOBT is chosen as screen<strong>in</strong>g technique<br />

the unrehydrated home-adm<strong>in</strong>istered FOBT is univocally recommended. All<br />

guidel<strong>in</strong>es also recommend total colonoscopy as the first choice method for<br />

<strong>in</strong>dividuals at <strong>in</strong>creased CRC risk as well as for surveillance. Guidel<strong>in</strong>es on

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