Distinct clinicopathological features and treatment differences in breast cancer patients of young age

The incidence of breast cancer in young women (aged under 40) is on the rise and is associated with more aggressive tumor characteristics and lower survival rates. Breast cancer is most frequently diagnosed in the sixth decade, and most research presents results based on data from older patients. By using large-scale clinico-pathologic and transcriptomic data from the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC) (n = 1932), we aimed to explore age-related differences in treatment, tumor characteristics, and gene expression signatures. Young patients presented more aggressive clinico-pathologic features such as higher histological grade, more frequent lymph node metastasis involvement, and estrogen receptor negativity. Accordingly, age below 40 years was associated with lower mRNA expression of the estrogen- and progesterone receptors, encoded by ESR1 and PGR, a higher proportion of the basal-like subtype, and increased transcription patterns reflecting stemness. Young breast cancer patients showed reduced survival, also within the basal-like subtype. We observed age-related differences in treatment, with more patients receiving chemotherapy among the young. Our results confirm a more challenging disease in young patients with breast cancer despite the more abundant use of chemotherapy. This argues for increased attention to young patients in current management and future research in breast cancer.

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Publication Details

Journal
Scientific Reports
Published
2025-02-15
DOI
https://doi.org/10.1038/s41598-025-90053-9
Citations
8
Primary Topic
Breast Cancer Treatment Studies
Type
article
Field-Weighted Citation Impact
7.49
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article

Distinct clinicopathological features and treatment differences in breast cancer patients of young age

Anna Kristine Myrmel Sæle, Erling A. Høivik, Lars A. Akslen, Rasmus O. C. Humlevik et al.
8 citations
Scientific Reports
Breast Cancer Treatment Studies
7.49
article

Distinct clinicopathological features and treatment differences in breast cancer patients of young age

Anna Kristine Myrmel Sæle, Erling A. Høivik, Lars A. Akslen, Rasmus O. C. Humlevik, Amalie A. Svanøe, Anette Heie, Elisabeth Wik, Turid Aas
article en
8 citations

Abstract

The incidence of breast cancer in young women (aged under 40) is on the rise and is associated with more aggressive tumor characteristics and lower survival rates. Breast cancer is most frequently diagnosed in the sixth decade, and most research presents results based on data from older patients. By using large-scale clinico-pathologic and transcriptomic data from the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC) (n = 1932), we aimed to explore age-related differences in treatment, tumor characteristics, and gene expression signatures. Young patients presented more aggressive clinico-pathologic features such as higher histological grade, more frequent lymph node metastasis involvement, and estrogen receptor negativity. Accordingly, age below 40 years was associated with lower mRNA expression of the estrogen- and progesterone receptors, encoded by ESR1 and PGR, a higher proportion of the basal-like subtype, and increased transcription patterns reflecting stemness. Young breast cancer patients showed reduced survival, also within the basal-like subtype. We observed age-related differences in treatment, with more patients receiving chemotherapy among the young. Our results confirm a more challenging disease in young patients with breast cancer despite the more abundant use of chemotherapy. This argues for increased attention to young patients in current management and future research in breast cancer.

Scientific ReportsVol. 15(1)
Haukeland University Hospital (NO), University of Bergen (NO)
Good health and well-being
Openalex Percentile: Top 3%
Breast Cancer Treatment Studies
7.49
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Distinct clinicopathological features and treatment differences in breast cancer patients of young age — Anna Kristine Myrmel Sæle, Erling A. Høivik, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS