RESUMENCon el objetivo de determinar las características clínicas y pronósticas de los carcinomas de mama, según sus subtipos moleculares mediante la aplicación de marcadores de inmunohistoquímica, se realizó un estudio en 280 mujeres con cáncer infiltrante de mama unilateral, del 2009 al 2012. Se clasificó por técnicas de inmunohistoquímica en 4 subtipos: luminal A, luminal B, HER2 y triple negativo. Para determinar la influencia del tipo histológico y del subtipo molecular en la sobrevida global, se utilizó el método de Kaplan Meier. Se encontró que los carcinomas de mama fueron: luminal A con 105 (37,5%); luminal B con 88 (31,4%); carcinomas HER2 con 46 (16,4%), y triple negativo con 41 (14,6%). Se concluye que los carcinomas de tipo luminal fueron con mayor frecuencia tumores bien diferenciados, con ganglios axilares negativos, tamaño tumoral y estadio semejante; mientras que los tumores HER2 y triple negativo presentaron mayor proporción de tumores pobremente diferenciados, compromiso ganglionar axilar, y menor sobrevida global.Palabras clave: Neoplasias de la mama; Inmunohistoquimica; Mastectomía; Carcinoma (fuente: DeCS BIREME).
CLINICAL AND PROGNOSTIC CHARACTERISTICS OF THE MOLECULAR SUBTYPES OF BREAST CANCER DETERMINED BY IMMUNOHISTOCHEMISTRY. AREQUIPA, PERU ABSTRACTThe objective of this study was to determine the clinical and prognostic characteristics of breast carcinomas according to the molecular subtype using immunohistochemical markers. The study included 280 women with unilateral breast cancer enrolled from 2009 to 2012. The carcinomas were classified into four subtypes based on immunohistochemical findings: luminal A, luminal B, HER2, and triple negative. The Kaplan-Meier test was used to determine the effect of histological type and molecular subtype on overall survival. Our results indicated that the most common breast carcinoma subtype was luminal A (105 cases, 37.5%), followed by luminal B (88 cases, 31.4%), HER2 (46 cases, 16.4%), and triple negative (41 cases, 14.6%). Luminal carcinomas were well-differentiated in most cases, without involvement of the axillary lymph nodes, and showed a similar tumor size and stage. In contrast, HER2 and triple-negative tumors were poorly differentiated in most cases, with axillary node involvement, and were associated with decreased overall survival.