Colorectal cancer (bowel cancer)
| Age | 0 - 9 | 10 - 14 | 15 - 19 | 20 - 24 | 25 - 29 | 30 - 34 | 35 - 39 | 40 - 44 | 45 - 49 | 50 - 54 | 55 - 59 | 60 - 64 | 65 - 69 | 70 - 79 | >80 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| X | X | X | X | 75 | |||||||||||
| High risk | X | X | X | X | X | X | X | X | X | X | X |
Organised screening by faecal occult blood testing (FOBT) is recommended for the asymptomatic average risk population from 50 years of age every 2 years (A) until 75 years of age with repeated negative findings.404,405 Increased risk is determined by family history and this should include determining the number of relatives affected by CRC, side of family and age at onset. Digital rectal examination (DRE) is not recommended as a screening tool (D) but should be used as part of an investigation of patients who present with symptoms such as rectal bleeding.
A GP recommendation can positively influence participation in bowel cancer screening using FOBTs.406,407
| Who is at higher risk of bowel cancer? | What should be done? | How often? | Level of evidence and references |
|---|---|---|---|
| Category 1 – average or slightly increased risk |
|
||
Asymptomatic people with:
|
FOBT | Every 2 years from 50 years of age | I A 86,404 408,409 |
Category 2 – moderately increased risk
| Colonoscopy (sigmoidoscopy plus double contrast barium enema) or CT colonography (performed by an experienced operator) acceptable if colonoscopy is contraindicated |
Every 5 years from 50 years of age, or at an age 10 years younger than the age of first diagnosis of CRC in the family, whichever comes first |
III B 404,410,411 |
| Consider offering FOBT | In intervening years | ||
|
Category 3 – high risk Asymptomatic people with:
OR
OR
OR
(Members of proven FAP and HNPCC families who test negatively for the mutation are no longer at high risk and revert to the moderately at risk group but still require surveillance) * HNPCC related cancers include cancer of the endometrium, ovary, pancreas, hepatobiliary tract, stomach, small intestine (usually duodenum or jejunum), upper urinary tract (transitional cell carcinoma of ureter and renal pelvis), brain (glioblastoma) |
Refer for genetic screening of affected relatives Refer to bowel cancer specialist to plan appropriate surveillance FAP: flexible sigmoidoscopy HNPCC: colonoscopy FOBT |
HNPCC:
Alternate years |
III B 404,410,411 |
| Test | Technique | References |
|---|---|---|
| Faecal occult blood test screening | Two main types of FOBT are available: guaiac and immunochemical tests. Two or three serial stools should be tested, depending on the type and brand of test being used. Follow the manufacturer’s instructions. It is essential that any positive FOBT (including just one of the samples) be appropriately investigated by diagnostic tests as these people are at least 12 times more likely to have CRC than someone with a negative test. With guaiac tests, even if a subject fails to follow dietary restrictions, it is dangerous to assume that a positive result is a result of dietary noncompliance | 404,406 |
Strategy
Measures to increase screening in these groups include recall and reminders, community outreach and links to other community services and organisations (see the ‘green book’).
The National Bowel Cancer Screening Program commenced in 2006 targeting specific age groups. General practitioners play a critical role in this program in terms of maximising participation, managing participants with a positive FOBT and providing information to the program about the investigation of people with a positive FOBT.412
© The Royal Australian College of General Practitioners
Printed from www.racgp.org.au/redbook



