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

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

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

1.4 SCREENING VERSUS SURVEILLANCE<br />

The New Zealand Guidel<strong>in</strong>es Group 27 def<strong>in</strong>es screen<strong>in</strong>g and surveillance as<br />

follows:<br />

1. Screen<strong>in</strong>g is the exam<strong>in</strong>ation of asymptomatic <strong>in</strong>dividuals <strong>in</strong><br />

order to classify them as unlikely or likely to have a disease. A<br />

national screen<strong>in</strong>g program is an example of a population<br />

preventive strategy, where everyone <strong>in</strong> a particular age-group is<br />

<strong>in</strong>vited to participate. Such strategy has the potential to identify<br />

a high proportion of <strong>in</strong>dividuals <strong>with</strong> early disease <strong>in</strong> a given<br />

population. This proportion depends on the uptake of screen<strong>in</strong>g<br />

and the sensitivity of the test chosen. Even <strong>in</strong> cancer screen<strong>in</strong>g<br />

programs where uptake is high and the screen<strong>in</strong>g test is very<br />

sensitive, the vast majority of <strong>in</strong>dividuals who take part will not<br />

have cancer, so that the potential benefits of screen<strong>in</strong>g are<br />

available to a relatively small group.<br />

2. Surveillance, as opposed to screen<strong>in</strong>g, refers to monitor<strong>in</strong>g<br />

<strong>in</strong>dividuals known to have a disease or to be at <strong>in</strong>creased risk<br />

for a disease. For this population the potential benefit of<br />

surveillance is higher than that of screen<strong>in</strong>g <strong>in</strong> the population at<br />

large, because the prevalence of the disease is higher <strong>in</strong> this<br />

population. Thus, the benefit-to-risk ratio of surveillance is more<br />

favourable than the benefit-to-risk ratio of screen<strong>in</strong>g. Therefore,<br />

for example, <strong>in</strong>dividuals who believe themselves to be at<br />

<strong>in</strong>creased risk of develop<strong>in</strong>g colorectal cancer (CRC) may be<br />

more will<strong>in</strong>g to accept the risks associated <strong>with</strong> surveillance.<br />

Others 28, 29 more restrictively def<strong>in</strong>e surveillance as monitor<strong>in</strong>g of patients<br />

known to have a specific disease or a genetic predisposition to it and screen<strong>in</strong>g<br />

as the exam<strong>in</strong>ation of <strong>in</strong>dividuals not (yet) known to have it, irrespective of the<br />

risk (average or <strong>in</strong>creased). In this def<strong>in</strong>ition screen<strong>in</strong>g can either refer to a<br />

population based screen<strong>in</strong>g program (average risk screen<strong>in</strong>g, population or mass<br />

screen<strong>in</strong>g), or to targeted screen<strong>in</strong>g for <strong>in</strong>dividuals <strong>with</strong> established risk factors<br />

or personal concerns about it (also called sensitive screen<strong>in</strong>g). Both methods<br />

imply different objectives and thus different requirements: if the aim is to<br />

reduce the burden of disease on a community the approach needed is<br />

population screen<strong>in</strong>g; this requires the use of a test associated <strong>with</strong> a high<br />

uptake and low cost. If, on the other hand, the aim is to respond to an<br />

<strong>in</strong>dividual s request for <strong>in</strong>formation regard<strong>in</strong>g his disease status, the emphasis<br />

must be on a test of high sensitivity and specificity 30.<br />

1.5 IMPLICATIONS FOR COLORECTAL CANCER SCREENING<br />

In deal<strong>in</strong>g <strong>with</strong> guidel<strong>in</strong>es for CRC screen<strong>in</strong>g, one must recognize that <strong>in</strong> many<br />

countries sensitive case f<strong>in</strong>d<strong>in</strong>g on an <strong>in</strong>dividual basis forms the foundation of<br />

so-called screen<strong>in</strong>g 31. Implementation of CRC mass screen<strong>in</strong>g programs is<br />

<strong>in</strong>deed tedious, expensive and requires several barriers to be overcome. It<br />

might therefore seem logical <strong>in</strong> some countries to concentrate public health<br />

resources on a selected sub-population, <strong>in</strong> which screen<strong>in</strong>g appears to be most<br />

mean<strong>in</strong>gful and probably more cost-effective.<br />

Return<strong>in</strong>g to def<strong>in</strong>itions, we have to recognize that the demarcation l<strong>in</strong>e<br />

between surveillance and targeted screen<strong>in</strong>g rema<strong>in</strong>s fuzzy: should we consider<br />

a proven genetic predisposition as a pre-cl<strong>in</strong>ical phase of the disease and thus<br />

need<strong>in</strong>g surveillance (follow-up)? And what should be done for patients <strong>with</strong> a

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