Colorectal (bowel) cancer is common in Australia, with about 14,800 new cases each year and a lifetime risk of approximately 1 in 23 by age 85. Screening detects occult bleeding from cancers and precancerous lesions before symptoms develop.
- Average-risk screening
- iFOBT every 2 years from age 45–74 years.
- Age 45–49: eligible for the National Bowel Cancer Screening Program (NBCSP), but must request the first free kit or obtain one through their healthcare provider.
- Age 50–74: kits are automatically mailed every 2 years.
- After completing a kit, subsequent kits are automatically sent every 2 years until age 74.
- Colonoscopy is not recommended as routine screening for average-risk asymptomatic people.
- iFOBT
- Detects small amounts of blood in stool that may arise from colorectal cancer or adenomas.
- Negative iFOBT does not exclude bowel cancer.
- Positive iFOBT → diagnostic assessment, usually colonoscopy.
- Do not use screening iFOBT to investigate symptoms.
- Family history – Category 1: average or slightly increased risk
- No family history, or
- 1 first-degree relative diagnosed at ≥60 years.
- Screening remains iFOBT every 2 years from 45–74 years.
- Family history at this level does not justify screening colonoscopy.
- Family history – Category 2: moderately increased risk
- 1 first-degree relative diagnosed <60 years, or
- 1 first-degree + ≥1 second-degree relative diagnosed at any age, or
- 2 first-degree relatives diagnosed at any age.
- Risk is approximately 2–4 times average.
- Colonoscopy every 5 years from:
- 10 years younger than the earliest diagnosis in a first-degree relative, or
- age 50,
- whichever is earlier.
- Continue to age 74.
- Family history – Category 3: potentially high risk
- Where Lynch syndrome has been excluded:
- 2 first-degree + 1 second-degree relative, with ≥1 diagnosed <50 years, or
- 2 first-degree + ≥2 second-degree relatives diagnosed at any age, or
- ≥3 first-degree relatives diagnosed at any age.
- Risk is approximately 4–20 times average.
- Colonoscopy every 5 years from:
- 10 years younger than the earliest diagnosis in a first-degree relative, or
- age 40,
- whichever is earlier.
- Continue to age 74.
- Consider referral to a familial cancer / clinical genetics service.
- For expanded detail: Genetic Counselling
- Where Lynch syndrome has been excluded:
- Hereditary colorectal cancer syndromes
- Lynch syndrome, familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) require syndrome-specific surveillance.
- Do not apply the generic Category 3 schedule to a known hereditary cancer syndrome.
- Refer for genetics/familial cancer assessment where the pedigree suggests inherited cancer susceptibility.
- Particularly consider referral with:
- colorectal cancer <50 years
- multiple Lynch-associated cancers in one person
- multiple affected close relatives
- colorectal and endometrial cancers within the family.
- For expanded detail: Genetic Counselling
- Previous colorectal cancer, adenomas or inflammatory bowel disease
- These patients require surveillance, not population screening.
- Surveillance intervals depend on previous cancer, polyp findings and underlying disease.
- Long-standing ulcerative colitis and Crohn colitis increase colorectal cancer risk.
- For expanded detail: Follow-up Post Colorectal Cancer
- Symptoms are not screening
- Rectal bleeding
- persistent change in bowel habit
- unexplained iron deficiency anaemia
- unexplained weight loss
- abdominal or rectal mass.
- These require diagnostic investigation regardless of age or previous screening results.
- DRE is not a population screening test, but may be appropriate when investigating symptoms.
- Aspirin
- For people at higher-than-average colorectal cancer risk, consider aspirin 100 mg daily from age 45–70 years after discussing benefits and bleeding risk.
- The previous advice of 100–300 mg from age 50–70 for ≥2.5 years is no longer the clean current Red Book recommendation.
- What does a positive iFOBT mean?
- In 2024, approximately 5.8% of NBCSP screening tests were positive.
- Among people with a recorded diagnostic assessment after a positive result:
- about 1 in 29 had confirmed or suspected bowel cancer
- about 1 in 3 had an adenoma.
- Therefore, most positive iFOBTs are not cancer, but the probability of important colorectal pathology is high enough that follow-up is essential.
- Risk reduction
- Eat plenty of vegetables, fruit and whole grains.
- Minimise red meat, processed meat and heavily grilled/barbecued meat.
- Maintain a healthy weight.
- Exercise regularly.
- Limit alcohol.
- Do not smoke.
The useful exam skeleton
- Average risk → iFOBT q2y age 45–74
- Positive iFOBT → colonoscopy
- 1 FDR ≥60 → iFOBT
- 1 FDR <60 / 2 FDR → Category 2 → colonoscopy q5y from 50 or 10 years before
- Heavy family history → Category 3 → colonoscopy q5y from 40 or 10 years before
- Lynch / FAP / MAP → specialist genetic pathway
- Symptoms → investigate, don’t screen