CLINICAL BREAST CANCER, vol.21, no.6, 2021 (Journal Indexed in SCI)
Next-generation sequencing has increased the detection of pathogenic/likely pathogenic variants in genes other than BRCA1/2. This study included 188 high-risk patients with BRCA1/2-negative breast cancer tested with a multigene cancer panel. Among 188 proband cases, 18 variants in 21 patients (11.1%) were classified as pathogenic/likely pathogenic. A multigene panel increased the diagnosis success in patients with BRCA1/2-negative high-risk breast cancer.