There is clear evidence the risk of bowel cancer is increased by tobacco smoking, alcohol, overweight and obesity, low physical activity and dietary factors such as low fibre and the consumption of red and processed meat.1 These risk factors should be assessed and information and support offered to modify them, wherever practicable, in primary care settings. All adolescent and adult Aboriginal and Torres Strait Islander people should be offered culturally appropriate preventive advice and asked specifically about any family history of bowel cancer. This could be assessed, documented, discussed and updated at an annual health assessment and communicated through tailored health promotion and community awareness activities. Cultural safety is a key aspect of asking about family history among Aboriginal and Torres Strait Islander peoples given the impact of colonisation, racism, forced removal of children from families and communities and intergenerational trauma.
Primary preventive activities that can be discussed with all adults and inform community health promotion messaging include the following:1,14
- not smoking (tobacco is an established cause of up to 8% of bowel cancer)
- eating a high-fibre diet
- maintaining a healthy body weight and avoiding abdominal obesity
- aiming for 30–60 minutes per day of at least moderate physical activity
- limiting alcohol intake to a maximum of four standard drinks per day and not more than 10 standard drinks per week
- limiting the consumption of red meat (especially when cooked until charred) and processed meats.
Refer to Chapter 2: Healthy living and health risks, Healthy eating, Physical activity and sedentary behaviour, Smoking and Alcohol and Chapter 15: Overweight and obesity.
Medication
Chemoprevention of bowel cancer for at least 2.5 years with low-dose (100–300 mg) daily aspirin for people aged 50–70 years with an average risk has been shown to reduce bowel cancer risk 10 years after the initiation of aspirin.5 The 2017 Australian guidelines recommend active consideration of aspirin in this group, particularly if there is added benefit of reducing cardiovascular and cerebrovascular events and thrombotic stroke. (A review of this was not included in the recently published guideline updates.) However, in clinical practice, aspirin is rarely used purely to prevent bowel cancer, except in the context of Lynch syndrome and familial adenomatous polyposis (J Keck, pers. comm., 2023), which is in line with Cancer Council Australia clinical practice guidelines for these high-risk conditions.2 The choice to take aspirin can be considered and personalised based on age and sex and a holistic health lens, including the additional potential reduction in cardiovascular events, but also considering the risk of bleeding and renal impairment.3,5
There is no current evidence for benefit over harms for the use of metformin, non-steroidal anti-inflammatory drugs (except aspirin), statins or bisphosphonates in the chemoprevention of bowel cancer at a population level.3
Screening
The NBCSP aims to reduce morbidity and mortality from bowel cancer by actively recruiting and screening all eligible people aged45–74 years with an iFOBT every two years, followed by colonoscopy for those with positive screening results.3 Screening is for people who do not have any signs or symptoms of bowel cancer. NBCSP screening activity, results and follow-up, including of colonoscopy, are recorded on the NCSR. The NCSR provides results and prompts for screening and follow-up to participants, so it is important for healthcare providers to notify the NCSR when NBCSP screening is initiated by the health service/practice or when NBCSP screening should be deferred if screening has occurred outside the program (see Useful resources).
Other bowel cancer screening tests are available, including flexible sigmoidoscopy and colonoscopy, computed tomography colonography and multitarget DNA stool testing,15 but considerations including cost, risks associated with invasive procedures, accessibility and resource allocation mean that these modalities are not part of the current population-based screening program.3,16,17 Surveillance colonoscopy, rather than iFOBT screening, is recommended for high-risk individuals with known familial syndromes.5 It is important to clarify that patients with symptoms of macroscopic blood loss, change in bowel habits or a past history of bowel cancer should not participate in the screening program, but rather be referred directly for investigation and/or surveillance.15,17 In addition, screening for bowel cancer with an iFOBT is inappropriate for high-risk individuals with chronic inflammatory bowel disease or certain genetic disorders, and in such cases specialist input is advisable.15
Assessing level of risk based on family history
People with a family history of bowel cancer may be at higher risk. The level of added risk depends on the number and closeness of relatives, and age at diagnosis.5 The level of added risk in an asymptomatic person is well described and informs guidelines for the age of starting, mode and interval of screening and/or surveillance3 (see Box 1).