Personalised breast cancer prevention for women

AnteBC

Genetic risk test for of breast cancer
Clinical recommendations based on your personal risk level for prevention and early detection
Recommended for women aged 30-75
Official healthcare service

Original price was: 195.00 €.Current price is: 175.50 €.
October is Breast Cancer Awareness Month – get 10% off.
Offer valid until October 31.

Important information

E-mail *

Test results are connected to the e-mail you provide.

Post-test consultation

No

Yes (+50.00 €)

Additional test

AnteCRC (+40.00 €)

AnteCRC is a colorectal cancer genetic risk test. It is suitable for both sexes.

AnteMEL (+40.00 €)

AnteMEL is a melanoma genetic risk test. It is suitable for both sexes.

Service price:	175.50 €
Additional options total:
Order total:

The test results provide answers to the following questions:

View AnteBC sample report

What is my genetic risk level of breast cancer?
At what age should I start breast cancer screening?
Should I take additional measures to prevent breast cancer?
What can I do to reduce my risk of breast cancer?
What changes and symptoms do I need to look out for regarding breast cancer?

Changing people's lives

Early detection makes a difference

4

Every 4th woman gets cancer during their lifetime.
48%

In 48% of cases, breast cancer is widespread at the time of detection, meaning it has a poor prognosis.
99%

With timely detection of breast cancer, it is possible to achieve a 99% probability of recovery.

Personalised cancer prevention is an up-to-date solution aimed at minimising the potential impact of three different cancers by tailoring it to your genetic risk level.

Tests take into account your unique characteristics – genetic composition, sex, age and ethnicity – which make your results fully personalised.

Personalised cancer prevention is meant for all women aged 35-75.

Research has shown that the genetic predisposition of many cancers is due to variants in many genes, meaning it is polygenic. Antegenes assesses a person’s risk of developing cancer using polygenic risk score technology, which is developed based on extensive international research. The polygenic risk score (PRS) sums up information over hundreds to thousands of genetic variants in the human genome. By combining the PRS with a person’s background (origin, age and gender), we are able to calculate a person’s risk of developing cancer and provide medical advice on prevention and early detection.

Based on the test results, you will receive personalised preventive recommendations from leading medical experts in the field. This guidance includes when and how to initiate cancer screening and other effective strategies to reduce your risks.

Armed with scientifically backed and well-documented medical advice, you are equipped to take preventive measures within your local healthcare system to proactively protect your health.

Approved by doctors and customers

Over 16 000 tests taken

"Currently, a very large proportion of malignant tumors are diagnosed at a late stage, when the disease's prognosis for life is already poor. With personalised cancer prevention, it is possible to find an individual prevention plan for each person and, thanks to this, raise people's awareness of their health and possible risks."

Dr Kristina Kuhi Gynecologist-mammologist
"Since I am younger than the age of being called for breast cancer screening, it was important for me to take a genetic risk test to find out my own genetic risk assessment of breast cancer and what I can do at a younger age to maintain my health. I found out that I have a higher risk and I’m now advised to go for a mammography screening as early as age 40 and should do it every two years. This is why I strongly encourage and recommend this kind of genetic testing – it gave me a sense of peace."

Hanna, 32
"I am one of those who became a breast cancer survivor under the age of 50. But at the same time, I am very lucky because I knew about my high polygenic risk score earlier thanks to the Antegenes genetic risk test so I started having mammograms several years ago. My cancer that did not make itself felt at all was discovered during a regular annual check-up as a small and easily treatable cancer. Only the PRS showed a high risk of breast cancer; a later genetic test during treatment did not find any common mutations associated with cancer. Without the Antegenes test, I might not have suspected that it would be wise for me to have a breast examination before the age of 50."

Katrin, 48

We’re here to answer your questions

What does AnteBC test include?

Personalised breast cancer prevention is based on the AnteBC test, which includes genetic risk testing for breast cancer.
AnteBC Test Limitations
- AnteBC test is not used to diagnose breast cancer.
- An elevated risk estimated by the AnteBC test does not mean that you will develop breast cancer during their lifetime. Also, a moderate or lower risk does not mean that the probability of developing the diseases is zero.
- AnteBC test does not assess the risk of your family and relatives, i.e. polygenic risk score-based disease risks may not be transmitted directly from parents to children.
- AnteBC test does not analyze rare pathogenic mutations in genes that significantly increase the risk of breast cancer, such as BRCA1, BRCA2, CHEK2, PALB2, ATM, TP53, CDH1, STK11, and others.
- The AnteBC test is based on the most up-to-date scientific data, which may, however, be supplemented and changed in the future as additional information becomes available. The field of genetics is constantly evolving, which may lead to changes in risk assessments over time, as well as changes in test selection recommendations and clinical recommendations based on test results.
- Different polygenic risk scores predicting risks of the same trait may give different estimates of the individual’s risks due to differences in the genetic variants included in the models and their weights.
- The results of this test should be applied in context with other relevant clinical data. In addition to the possible genetic predisposition, other risk factors also influence the risk of breast cancer.

How it works?

1 Choose your tests
Select from our range of specialized tests tailored to your health and wellness needs.
2 Prepare for sampling
Receive easy-to-follow instructions for a convenient sample collection process in the comfort of your own home.
3 Provide a sample
Use the provided kit to collect a sample, following guidelines to capture the genetic information needed for testing.
4 Receive your results
Receive results quickly, accompanied by recommendations and guidance for your next steps.