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

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

4 Guidel<strong>in</strong>es for the<br />

Prevention, Early<br />

Detection and<br />

Management of<br />

Colorectal Cancer 50<br />

5 American Cancer<br />

Society guidel<strong>in</strong>es on<br />

screen<strong>in</strong>g and<br />

surveillance for the<br />

early detection of<br />

adenomatous polyps<br />

and colorectal cancer<br />

- update 200456 .<br />

6 Surveillance and<br />

management of<br />

groups at <strong>in</strong>creased<br />

risk of colorectal<br />

cancer27 .<br />

Australian Cancer Network<br />

Colorectal Cancer<br />

Guidel<strong>in</strong>es Revision<br />

Committee<br />

American Cancer Society<br />

(ACS)<br />

New Zealand Guidel<strong>in</strong>es<br />

Group (NZGG)<br />

2005 1 FDR <strong>with</strong> CRC diagnosed at 55 years<br />

or over (<strong>in</strong>cluded <strong>in</strong> category 1 RR up to<br />

2-fold)<br />

1 FDR <strong>with</strong> CRC diagnosed under 55<br />

years (RR 3 to 6-fold)<br />

2 FDR <strong>with</strong> CRC diagnosed at any age<br />

(RR 3 to 6-fold)<br />

2004 Either CRC or adenomatous polyps <strong>in</strong> any<br />

FDR < 60 y, or <strong>in</strong> 2 FDR at any age (if<br />

not a hereditary syndrome).<br />

CRC <strong>in</strong> relatives more distant than FDR<br />

does not <strong>in</strong>crease risk substantially above<br />

the average risk group<br />

2004 Category 3 risk:<br />

1 FDR plus 2 FDR or SDR, all on the<br />

same side of the family, <strong>with</strong> a diagnosis or<br />

CRC at any age<br />

2 FDR, or 1 FDR plus 1 SDR, all on<br />

the same side of the family, <strong>with</strong> a<br />

diagnosis of CRC and one such relative (1)<br />

was diagnosed <strong>with</strong> CRC under age of 55<br />

y, (2) developed multiple bowel cancers,<br />

or (3) developed an extra-colonic tumor<br />

suggestive of hereditary nonpolyposis<br />

colorectal cancer (i.e., endometrial,<br />

ovarian, stomach, small bowel, upper renal<br />

tract, pancreas, or bra<strong>in</strong>)<br />

At least 1 FDR or SDR diagnosed <strong>with</strong><br />

CRC <strong>in</strong> association <strong>with</strong> multiple bowel<br />

polyps<br />

1 FDR <strong>with</strong> CRC diagnosed < 50 y,<br />

particularly if colorectal tumor<br />

immunohistochemistry has revealed loss<br />

of prote<strong>in</strong> expression for one of the<br />

mismatch repair genes (hMLH1 or<br />

hMSH2)<br />

Colonoscopy<br />

FS and DCBE or CT<br />

colonography may be<br />

offered if colonoscopy is<br />

contra<strong>in</strong>dicated for some<br />

reason.<br />

50 y. or 10 years<br />

younger than the<br />

age of first<br />

diagnosis of<br />

bowel cancer <strong>in</strong><br />

the family,<br />

whichever<br />

comes first.<br />

Colonoscopy Age 40, or 10 y<br />

before the<br />

youngest case <strong>in</strong><br />

the immediate<br />

family<br />

Suspect hereditary<br />

disease and refer patient<br />

to:<br />

A genetic<br />

specialist/family cancer<br />

cl<strong>in</strong>ic or familial bowel<br />

cancer registry for<br />

further risk assessment<br />

and possible genetic<br />

test<strong>in</strong>g<br />

If yes see<br />

surveillance; if no <br />

colonoscopy<br />

40 y or 10 y<br />

younger than<br />

affected relative<br />

(whichever is<br />

younger),<br />

Repeat every 5<br />

y.<br />

Every 5-10 y Evidence<br />

discussed<br />

but not<br />

explicitly<br />

rated<br />

Repeat every 1-5<br />

y<br />

III-2 Recommended<br />

Grade 5<br />

N/A<br />

See Appendix 2<br />

NZGG National<br />

Health Committee<br />

evidence grad<strong>in</strong>g<br />

hierarchy

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