Breast cancer is the most common cancer in Australian women. About 1 in 7 women will be diagnosed during their lifetime. Around 20,000 Australians are diagnosed each year and 5-year survival is approximately 93%.
- Average-risk screening
- Mammogram every 2 years from age 50–74 years through BreastScreen Australia.
- Women aged 40–49 years may self-refer for free screening but are not routinely invited.
- Women aged ≥75 years can access BreastScreen, but routine screening is not generally recommended because evidence of net benefit is insufficient.
- Screening applies to asymptomatic women. A breast symptom requires diagnostic assessment, not routine screening.
- For expanded detail: Mammograms and Breast Augmentation
- Moderately increased familial risk
- Think:
- 1 first-degree relative diagnosed <50 years, or
- 2 first-degree relatives on the same side of the family, or
- 2 second-degree relatives on the same side, with ≥1 diagnosed <50 years.
- Consider mammographic screening from age 40–74 years, at least every 2 years.
- Some women may warrant annual mammography from age 40.
- Think:
- Potentially high familial / genetic risk
- Think multiple cancers on one side of the family plus red flags:
- breast cancer <40 years
- bilateral breast cancer
- breast and ovarian cancer in the same person
- male breast cancer
- Ashkenazi Jewish ancestry
- known pathogenic familial variant such as BRCA1/BRCA2.
- Also remember paternal family history counts just as much as maternal history.
- Refer to a familial cancer service / genetics service for formal risk assessment, genetic counselling and consideration of testing.
- High-risk surveillance may include MRI plus mammography, rather than simply “more frequent BreastScreen”.
- For expanded detail: Genetic Counselling
- Think multiple cancers on one side of the family plus red flags:
- BRCA and other hereditary cancer testing
- Do not simply order BRCA testing as routine GP screening.
- Current MBS germline testing items for hereditary breast/ovarian cancer are restricted to testing requested by a specialist or consultant physician in patients meeting defined criteria.
- A GP’s role is to recognise the family-history pattern and refer for genetic assessment.
- Testing now commonly involves a multigene panel, not just BRCA1/BRCA2; relevant genes can include PALB2, TP53, PTEN, CDH1 and STK11.
- Public familial cancer services generally arrange testing without charge where criteria are met.
- Private genetic testing is available, but cost varies by laboratory and panel; there is no useful single national price to quote.
- For expanded detail: Genetic Counselling
- Family history changes risk
- 1 first-degree relative: about 2× risk
- 2 first-degree relatives: about 3× risk
- ≥3 affected relatives: about 4× risk
- Second-degree relative(s): about 1.5× risk
- Risk rises further when relatives are diagnosed young, particularly <50 years.
- Clinical breast examination and self-examination
- Routine clinical breast examination is not recommended for screening average-risk asymptomatic women.
- Formal scheduled breast self-examination — eg “every 3 months” — is not the current recommendation.
- Instead teach breast awareness: know what is normal and report a new or unusual change promptly.
- Important changes include:
- new lump or lumpiness
- nipple inversion, crusting or discharge
- change in breast size or shape
- skin dimpling or redness
- persistent unusual breast pain.
- There is no preferred technique or interval for checking the breasts.
- What not to use for average-risk screening
- MRI alone is not a screening test for average-risk women.
- Thermography is not recommended.
- Supplemental ultrasound or MRI solely for dense breasts remains an area where evidence of benefit versus harm is insufficient.
- High-risk women are different: MRI may form part of specialist surveillance.
- Benefits and harms
- Mammography reduces breast cancer mortality through earlier detection.
- Harms include:
- false positives
- unnecessary biopsies
- anxiety
- overdiagnosis and overtreatment.
- The balance of benefit is strongest in the 50–74 year target group.