Clinical characteristics of male patients with breast cancer in the Latino population

Breast cancer is the most prevalent cancer type in Mexico, with male breast cancer accounting for only 1% of all breast cancer cases. A limited number of studies have described the clinical-pathological profiles of males with breast cancer in low- and middle-income countries. This study presents an...

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Veröffentlicht in:Breast cancer research and treatment 2024-10
Hauptverfasser: González-Nuñez, Carlos, Mohar, Alejandro, Reynoso-Noverón, Nancy, Alvarez-Gómez, Rosa María, Chavarri-Guerra, Yanin, Aguilar-Villanueva, Sergio, Guzmán-Trigueros, Raúl, Velázquez-Martínez, Areli, Wegman-Ostrosky, Talía, Porras-Reyes, Fanny, Garcilazo, Alexandra, Arce, Claudia, Bargallo-Rocha, Juan Enrique, Cabrera-Galeana, Paula
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Sprache:eng
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Zusammenfassung:Breast cancer is the most prevalent cancer type in Mexico, with male breast cancer accounting for only 1% of all breast cancer cases. A limited number of studies have described the clinical-pathological profiles of males with breast cancer in low- and middle-income countries. This study presents an analysis of patients with breast cancer seen at three different institutions in México. A retrospective review of the medical records was performed to analyze the clinical and pathological characteristics of 49 men diagnosed with breast cancer and their overall survival. The mean age at diagnosis was 64.65 years. A significant proportion of patients presented at diagnosis with stage IV disease (n = 11, 22.45%), had triple-negative subtype (n = 6, 12.24%), and nuclear grade III (n = 20, 40.8%). Primary endocrine resistance was observed in 10 patients (31.25%). Genetic analysis was performed on 24 patients (48.9%), revealing a germline BRCA pathogenic variant in 8.33%. Our findings described the clinical and pathological profile of breast cancer in a male cohort in Mexico, with a significantly high proportion of advanced disease, triple-negative subtype, nuclear grade III, and endocrine resistance. Further comprehensive studies, including research into somatic mutations, are needed.
ISSN:0167-6806
1573-7217
1573-7217
DOI:10.1007/s10549-024-07525-1