Key result
Breast cancer survivorship is linked to ~68% higher VTE risk vs matched controls.
Why the study?
Venous thromboembolism is a serious complication for breast cancer survivors.
Does a history of breast cancer increase the risk of venous thromboembolism in women compared to those without a cancer history?
Cohort (n=450,088)
Yes
Does a history of breast cancer increase the risk of venous thromboembolism in women compared to those without a cancer history?
Hazard Ratio: 1.68 (95% CI 1.61–1.75)
Female breast cancer survivors have a significantly elevated mid- and long-term risk of venous thromboembolism, particularly in the first year post-diagnosis and with certain chemotherapies, highlighting the need for VTE risk assessment.
BC survivors face elevated VTE risk, highest early post-diagnosis; leaves open optimal prevention strategies in this population.
Venous thromboembolism (VTE) is a serious complication for breast cancer (BC) survivors. We identified records of female BC survivors from the Korean Health Insurance Service database between January 1, 2010, and December 31, 2016. After applying exclusion criteria (age < 18 years, prior cancers or VTE, absence of BC surgery, or missing data), 112,522 BC survivors were included; for the comparison group, BC survivors were matched (1:3) to women without cancer history. VTE risk was evaluated with a Fine and Gray model, accounting for death as a competing risk; multiple time periods were analyzed. Associations between VTE risk and treatment modalities also were estimated. Over a mean analysis period of 7.4 years, BC survivors had 3621 VTE events; their subdistribution hazard ratio (sHR) for VTE was greater than that of the comparison group (sHR 1.68, 95% CI 1.61-1.75). The risk was prominent within the first year post-diagnosis (sHR 7.78, 95% CI 6.88-8.80) and attenuated in analyses restricted to VTE events occurring beyond 1 year after diagnosis (sHR 1.34, 95% CI 1.28-1.40), but remained significantly elevated in landmark (delayed-entry) analyses starting at later time points. Anthracycline (sHR 1.11, 95% CI 1.00-1.23) and taxane (sHR 1.73, 95% CI 1.57-1.91) therapies were associated with an increased risk of VTE in 1-year landmark analysis. Female BC survivors are at increased risk of VTE, especially during the first year post-diagnosis, which underscores the importance of VTE risk assessment for BC survivors.
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Kang et al. (2026) conducted a cohort in Breast cancer (n=450,088). Breast cancer survivorship vs. Women without cancer history was evaluated on Venous thromboembolism (VTE) (sHR 1.68, 95% CI 1.61-1.75). Female breast cancer survivors had a significantly higher risk of venous thromboembolism compared to matched women without cancer history (sHR 1.68; 95% CI 1.61-1.75).
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