Background We aimed to clarify the features of adolescents and young adults (AYA: younger than 40yo) breast cancer (BC) compared with other age groups in ER-positive/HER2-negative BC, given the effects of age-related hormonal status. Methods The cohorts analyzed were divided into: AYA (15-39yo), Perimenopausal (40-54yo), Menopausal (55-64yo), and Old (65 + yo). Clinicopathological and biological features were analyzed using gene set variation analysis and the xCell algorithm using transcriptome profiles from large public databases of ER-positive/HER2-negative BC (METABRIC; n = 1,353, SCAN-B; n = 2,381). Results Tumors were larger and more advanced among the AYA and Old age groups than among the other groups. Pathological lymph node positivity and Nottingham grade 3 were higher among AYA. AYA was significantly associated with triple-negative BC and higher HER2-positivity. AYA had poorer disease-specific and overall survival particularly compared to perimenopausal group. In the ER-positive/HER2-negative subtype, estrogen response late signaling decreased with age. AYA was associated with significantly higher BRCAness and DNA repair than the other groups. AYA significantly enriched cell proliferation-related and pro-cancerous gene sets (MTORC1, unfolded protein response, and PI3K/AKT/MTOR signaling) when compared to the others. Interestingly, these features have also been observed in small tumors. Infiltration of CD8+, regulatory, and helper type 2 T cells, and M1 macrophages was higher, while M2 macrophages were lower in AYA. Finally, ER-positive/HER2-negative BC in AYA patients has different features of gene mutations compared to other age groups. Conclusions ER-positive/HER2-negative BC in AYA was highly proliferative with high immune cell infiltration compared to other generations.
No takes yet. Share an insight, caveat, or question.
Oshi et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: