Abstract
Objective. Describe the prevalence of breast cancer (BC)- associated germline pathogenic variants (PVs) among Mexican patients with triple-negative BC (TNBC). Materials and methods. The spectrum of PVs identified among patients with TNBC who were enrolled in a prospective registry and underwent genetic testing was analyzed. Results. Of 387 patients with invasive TNBC and a median age at diagnosis of 39 years (range 21-72), 113 (29%) were carriers of PVs in BC-susceptibility genes: BRCA1 (79%), BRCA2 (15%), and other (6%: ATM, BRIP1, PALB2, PTEN, RAD51C, and TP53). PV carriers were younger at BC diagnosis (37 vs. 40 years, p=0.004) than non-carriers. Conclusion. A large proportion of TNBC in Mexican patients is associated with germline PVs, the vast majority in BRCA. The incremental yield of PVs in other BC-susceptibility genes was modest, and a stepwise approach starting with BRCA testing may be justified if it is more costeffective than multigene panel testing.
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Chavarri-Guerra, Y., Villarreal-Garza, C., Ferrigno, A. S., Mohar-Betancourt, A., Aguilar, D., Alvarez-Gomez, R. M., … Weitzel, J. N. (2022). Germline pathogenic variants in Mexican patients with hereditary triple-negative breast cancer. Salud Publica de Mexico, 64(1), 41–48. https://doi.org/10.21149/12704
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