Home > Publications database > Prognostic role of pre-diagnostic circulating inflammatory biomarkers in breast cancer survival: evidence from the EPIC cohort study. |
Journal Article | DKFZ-2024-02193 |
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2024
Nature Publ. Group
Edinburgh
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Please use a persistent id in citations: doi:10.1038/s41416-024-02858-6
Abstract: Inflammation influences tumour progression and cancer prognosis, but its role preceding breast cancer (BC) and its prognostic implications remain inconclusive.We studied pre-diagnostic plasma inflammatory biomarkers in 1538 women with BC from the EPIC study. Cox proportional hazards models assessed their relationship with all-cause and BC-specific mortality, adjusting for tumour characteristics and lifestyle factors.Over a 7-year follow-up after diagnosis, 229 women died, 163 from BC. Elevated IL-6 levels were associated with increased all-cause mortality risk (HR1-SD 1.25, 95% CI 1.07-1.47). Among postmenopausal, IL-6 was associated with higher all-cause (HR1-SD 1.41, 95% CI 1.18-1.69) and BC-specific mortality (HR1-SD 1.31, 95% CI 1.03-1.66), (PHeterogeneity (pre/postmenopausal) < 0.05 for both), while IL-10 and TNFα were associated with all-cause mortality only (HR1-SD 1.19, 95% CI 1.02-1.40 and HR1-SD 1.28, 95% CI 1.06-1.56). Among ER+PR+, IL-10 was associated with all-cause and BC-specific mortality (HR1-SD 1.35, 95% CI 1.10-1.65 and HR1-SD 1.42 95% CI 1.08-1.86), while TNF-α was associated with all-cause mortality in HER2- (HR1-SD 1.31, 95% CI 1.07-1.61). An inflammatory score predicted higher all-cause mortality, especially in postmenopausal women (HR1-SD 1.30, 95% CI 1.07-1.58).Higher pre-diagnosis IL-6 levels suggest poorer long-term survival among BC survivors. In postmenopausal survivors, elevated IL-6, IL-10, and TNFα and inflammatory scores seem to predict all-cause mortality.
Keyword(s): Humans (MeSH) ; Female (MeSH) ; Breast Neoplasms: mortality (MeSH) ; Breast Neoplasms: blood (MeSH) ; Breast Neoplasms: diagnosis (MeSH) ; Breast Neoplasms: pathology (MeSH) ; Middle Aged (MeSH) ; Prognosis (MeSH) ; Inflammation: blood (MeSH) ; Inflammation: mortality (MeSH) ; Biomarkers, Tumor: blood (MeSH) ; Interleukin-6: blood (MeSH) ; Aged (MeSH) ; Postmenopause: blood (MeSH) ; Cohort Studies (MeSH) ; Interleukin-10: blood (MeSH) ; Adult (MeSH) ; Tumor Necrosis Factor-alpha: blood (MeSH) ; Proportional Hazards Models (MeSH) ; Biomarkers, Tumor ; Interleukin-6 ; Interleukin-10 ; Tumor Necrosis Factor-alpha ; IL6 protein, human ; IL10 protein, human
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