Borstkanker

Lagere overleving bij sociaaleconomisch achtergestelde vrouwen met HER2-negatieve borstkanker na chemotherapie

Canadees onderzoek toont aan dat sociaaleconomische achterstand een substantiële rol speelt bij de overleving van borstkankerpatiënten. Naast het tumorstadium en subtype beïnvloeden sociale determinanten de prognose significant.

Abstract (original)

BACKGROUND: Breast cancer remains the most common oncological condition and the leading cause of cancer-related mortality in the world. In addition to the breast cancer stage at diagnosis, its histology and subtype, the social determinants of health have a substantial role in cancer survivorship. METHODS: Utilizing administrative health databases, a retrospective analysis of stage I-III HER2-negative breast cancer was conducted, examining a cohort of 10,634 women treated with surgery and adjuvant chemotherapy in Ontario, Canada. RESULTS: Our study registered a median follow-up of 5.5 years. The 5-year OS ranging from the lowest to the highest socioeconomic status (SES) was (Q1) 91.3%, (Q2) 92.8%, (Q3) 93.0%, (Q4) 92.9% and (Q5) 94.0%. The 5-year OS rate between the SES groups showed (Q5 vs. Q1) HR 0.65 (95% CI, 0.52-0.81), P = .002), (Q4 vs. Q1) HR 0.79 (95% CI, 0.64-0.97, P = .029) and (Q3 vs. Q1) HR 0.75 (95% CI, 0.60-0.94, P = .013). In the analysis of underlying medical conditions, the mean range of the Charlson comorbidity index was Q1 (2.73 ± 2.96) versus Q5 (2.52 ± 2.63), P < .001. CONCLUSION: Our study shows that there are inequities in the delivery of oncological care amongst women with HER2-negative breast cancer. Those within the lower SES, thereby likely with a socioeconomic disadvantage, exhibited a greater probability of presenting with more advanced cancer staging, were more prone to receive anthracycline-based chemotherapy, while also being confronted with an increased likelihood of significant comorbidities and mortality rates, compared to their wealthier counterparts.

Dit artikel is een samenvatting van een publicatie in Clinical breast cancer. Voor het volledige artikel, alle details en referenties verwijzen wij u naar de oorspronkelijke bron.

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DOI: 10.1016/j.clbc.2026.02.015