Integrating Polygenic Scores into Multifactorial Breast Cancer Risk Assessment: Insights from the First Year of Clinical Implementation in Western Austria
<b>Background/Objectives:</b> The implementation of polygenic scores (PGSs) and multifactorial risk assessments (MFRAs) has the potential to enhance breast cancer risk stratification, particularly in carriers of moderate-penetrance pathogenic variants (PVs), whose risk profiles often remain unclear if testing is limited to monogenic risk factors. <b>Methods:</b> To enhance breast cancer risk stratification, we included the BCAC313 polygenic score, together with MFRA, for carriers of moderate-penetrance pathogenic variants (PVs) during routine diagnostics and assessed its effect on the classification of patients' risk categories in a real-world cohort at our center in its first year of implementation. Seventeen carriers with PVs in moderate-risk breast cancer genes were included in this study. Thirteen of them qualified for analysis for a full MFRA, including PGS, according to ancestry estimation and clinical criteria. The MFRA was performed using the CanRisk tool, which incorporates clinical, lifestyle, familial, and genetic data, including the BCAC313 score. <b>Results:</b> PGS z-scores were significantly higher in breast cancer patients compared to the unaffected control cohort (<i>p</i> = 0.016). The MFRA, including PGS, increased risk estimates for contralateral breast cancer in seven of eight patients with breast cancer and for primary breast cancer in three of five healthy carriers, compared to the risk conferred by the MFRA and moderate-penetrance pathogenic variant alone. Risk estimates varied widely, demonstrating the value of MFRA in personalized care. In five cases, one with a <i>CHEK2</i>-PV and four with an <i>ATM</i>-PV, the modified risk assessment contributed to the surgical decision for a prophylactic mastectomy. <b>Conclusions:</b> The MFRA, including PGS, provides the clinically meaningful refinement of breast cancer risk estimates in individuals with moderate-risk PVs. Personalized risk predictions can inform clinical management and support decision-making, which highlights the utility of this approach in clinical practice.
Authors
- Simon Schnaiter (ORCID: https://orcid.org/0009-0009-5213-6237)
- Gunda Schwaninger (ORCID: https://orcid.org/0000-0002-2120-848X)
- Lukas Forer (ORCID: https://orcid.org/0000-0003-2139-7329)
- Daniel Egle (ORCID: https://orcid.org/0000-0003-0283-8176)
- Florian Schnitzer
- Johannes Zschocke (ORCID: https://orcid.org/0000-0002-0046-8274)
- Kathrin Taxer
Institutions
- Innsbruck Medical University (AT)
- Health University of Applied Sciences Tyrol (AT)
- BrustGesundheitZentrum Tirol (AT)
Publication Details
- Journal
- Cancers
- Published
- 2025-07-26
- DOI
- https://doi.org/10.3390/cancers17152472
- Primary Topic
- BRCA gene mutations in cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00