Obstacles in genetic testing for germline BRCA1/2 pathogenic mutations in patients with primary breast and ovarian cancer in Switzerland
Timely, well-communicated recommendations and informational resources significantly improve genetic counseling uptake among breast and ovarian cancer patients. Addressing systemic and patient-specific barriers will enhance equitable access, optimize targeted therapies and preventive strategies, and should be supported by national registries, qualitative research, and digital integration.
Authors
- Christine Brambs (ORCID: https://orcid.org/0000-0001-7682-2172)
- Lucie Krautova
- Kathrin Schwedler
- Christian Braun (ORCID: https://orcid.org/0000-0001-7966-4085)
- Corina Christmann
Institutions
- University of Lucerne (CH)
- Luzerner Kantonsspital (CH)
Publication Details
- Journal
- Archives of Gynecology and Obstetrics
- Published
- 2025-08-09
- DOI
- https://doi.org/10.1007/s00404-025-08138-9
- Primary Topic
- BRCA gene mutations in cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00