Why Prevent Breast Cancer Supports PRS Testing

What is Polygenic Risk Score Testing?
A Polygenic Risk Score Test (PRS Test) estimates your risk of developing certain cancers, including breast cancer, based on your genes.
Instead of reviewing just one gene, it examines tiny DNA fragments called SNPs (Single Nucleotide Polymorphisms), which can affect your risk of developing breast cancer.
Most breast cancers are not caused just by genetics, but by a combination of genetic, environmental and lifestyle factors.
The polygenic risk score test is simple and non-invasive. Simply provide a saliva sample using a spit kit and fill out a short questionnaire.
By combining your genetic information with your personal and family history, the test gives you a personalised risk score for developing cancer.
On this page we will refer to the AnteBC Polygenic Risk Score Test, which is a type of PRS test offered privately by Prevent Cancer UK, as part of their Personalised Breast Cancer Prevention Plan service.
How Does the AnteBC Polygenic Risk Score Test Prevent Breast Cancer?
In the UK, NHS breast cancer screening starts at age 50, with mammograms offered every three years. Currently, most screenings are based on age and family history, rather than an individual’s personal level of risk.
Eventually, the polygenic risk score testing will move us towards preventative interventions based on who needs it most, rather than a one-size-fits-all model.
Results from an AnteBC polygenic risk score test could allow those with a high Polygenic Risk Score to receive preventative breast cancer treatments.
Is PRS Testing Different to BRCA1/2 Testing?
BRCA1/2 gene mutations are rare, occurring in 0.2 – 0.3% of women in the general population. BRCA1/2 tests are only performed in specific cases, such as when there is a strong family history of breast cancer.
Whereas polygenic risk score testing evaluates common genetic variations that influence breast cancer risk for all women, not just those with a strong family history.
As part of the Personalised Breast Cancer Prevention Plan, those with a strong family history will be advised to request NHS gene testing for high-risk genes such as BRCA1 and BRCA2.
Why is Prevent Breast Cancer Supporting AnteBC Polygenic Risk Score Test?
One of the ambitions of Prevent Breast Cancer is to see risk prediction tests made available to all women over 30 across the UK as an NHS screening service. At the present time, the NHS simply doesn’t have the funds or the staff to do this.
For those of you who wish to purchase private polygenic risk score gene testing, we can point you to Prevent Cancer UK as a reputable company who offers the AnteBC polygenic risk score test within their Personalised Breast Cancer Prevention Plan.
Who is the AnteBC Tests Targeted at?
The polygenic risk score test is currently only available privately. The AnteBC PRS test can be purchased on the Prevent Cancer UK website, meaning anyone can order the test. However, the test is targeted at women over the age of 30.
Can Men Take The Test?
Breast cancer in men is very rare and typically occurs in those with a strong family history and genetic risk factors (such as BRCA mutations). Prevent Cancer UK’s Breast Cancer Prevention services are calibrated for women only. However, personalised cancer prevention strategies for prostate cancer can provide significant benefits for men, helping them optimise their screening and prevention strategies.
Key Reasons Why Prevent Breast Cancer Supports This Personalised Breast Screening Service
What To Consider Before Taking the AnteBC Polygenic Risk Score Test
If your test result shows particularly high risk, then your GP may be able to refer you to an NHS clinic for advice on what to do. On the other hand, you may have to pay for any additional tests or scans yourself, adding to the final cost.
Please note that Prevent Breast Cancer cannot give you individual clinical advice on the results of a private test.Â
Promoting Fairer Breast Cancer Screening and Prevention
Although the initial model involves women choosing to pay for polygenic risk score testing, the insights gained could drive a shift towards more personalised, targeted, and ultimately more fair and inclusive breast cancer screening and prevention – ensuring that interventions are based on actual risk, not assumptions, and helping identify and support high-risk women who might otherwise be missed.
Ensuring Health Equity
At first glance, offering private polygenic risk score testing (especially when paid for by individuals) might seem like it risks creating unfairness, because not everyone can afford it.
However, if you design the programme carefully, it can support a more equitable approach overall to breast cancer prevention and screening.

Better Identification of Hidden Risk:
Traditional risk factors (like family history) miss a lot of women at high risk – particularly women from underrepresented groups who might not have complete family history records (e.g., smaller families, adoption, earlier deaths). Polygenic risk score testing gives everyone an opportunity to understand their personal genetic risk, beyond just those with obvious family histories.

Targeted Screening Based on Need, Not Assumptions:
Currently most breast screening is based on age, not individual risk.
PRS testing helps move towards screening based on who most needs it, rather than a one-size-fits-all model

Informing Future Public Provision:
Even if the first step involves women paying for polygenic risk score if they can afford it, the data collected can demonstrate the value of risk-based screening.
This evidence could strengthen the case for a polygenic risk score test to be offered free or subsidised in the NHS in the future, making personalised prevention accessible to all women, not just those who can pay.

Earlier Intervention for Underserved Groups:
By identifying high-risk women earlier (especially in communities that traditionally have lower screening uptake), polygenic risk score testing could lead to earlier interventions, improving survival rates across diverse populations.

Building Inclusive Risk Prediction Models:
Over time, offering polygenic risk score testing to a broader range of women will help improve and diversify the data that underpins the risk scores themselves, making them more accurate and fairer for women from different ethnicities and backgrounds.
What Happens After You Receive Your Results?
Based on your results, you will receive a personalised prevention plan post-test and will be advised should you need further testing based on your results.
It is important to understand that if your test result shows that you have a particularly high risk, you may have to pay privately for any additional tests or scans yourself, adding to the final cost.
Your GP may be able to refer you to an NHS clinic for advice on what to do, but this will depend on the type of results you receive, and if you meet NHS and NICE referral eligibility criteria.
Tailored Medical Recommendations
Laura Naylor, a Senior Breast Clinical Nurse Specialist and founder of The Breast Awareness Clinic, offers personalised genetic testing, as well as consultation and support, to assess an individual’s risk of breast cancer. In collaboration with Antegenes, Prevent Cancer UK, and Prevent Breast Cancer, she provides tailored medical recommendations based on each person’s unique genetic profile, empowering individuals to make informed choices about their breast health.
About Prevent Breast Cancer
Prevent Breast Cancer is the only UK charity entirely dedicated to the prediction and prevention of breast cancer – we’re committed to freeing the world from the disease altogether. Unlike many cancer charities, we’re focused on preventing, rather than curing. Promoting early diagnosis, screening and lifestyle changes, we believe we can stop the problem before it starts. And being situated at the only breast cancer prevention centre in the UK, we’re right at the front-line in the fight against the disease. Join us today and help us create a future free from breast cancer. If you have any questions or concerns, email us today.
on July 4, 2025.
on June 13, 2025.


