Key result
Long-term statin use linked to up to ~81% lower all-cause mortality in cancer survivors.
Why the study?
Does statin prescription reduce long-term all-cause mortality in Korean cancer survivors?
Cohort (n=154,916)
Yes
Does statin prescription reduce long-term all-cause mortality in Korean cancer survivors?
Effect estimate: HR 0.258 (men, T3) and 0.190 (women, T3) (95% CI 0.244-0.272 (men) and 0.178-0.203 (women))
p-value: p=<.001
Longer duration of statin prescription is associated with significantly lower long-term all-cause mortality among Korean cancer survivors.
Should not yet change statin prescribing in cancer survivors; leaves open potential survival benefit requiring randomized confirmation.
Cancer survivorship is rapidly increasing in Korea, and long-term outcomes are influenced not only by cancer progression but also by competing risks such as cardio-cerebrovascular disease. Statins, routinely prescribed for cardiovascular prevention, have pleiotropic anti-inflammatory and immunomodulatory properties and have been suggested to affect outcomes in patients with cancer. We investigated whether statin prescription was associated with long-term all-cause mortality using data from Korean nationwide health insurance claims. Patients were divided into 4 groups based on the duration of statin prescription: nonusers, T1, T2, and T3. Kaplan-Meier estimates and log-rank tests were performed to compare the survival rate among the 4 groups. Cox proportional hazards regression models were constructed for all-cause mortality. Among 154,916 patients, the median follow-up was 14.6 years, and the cumulative survival was lowest in statin nonusers and highest in T3 in both sexes (log-rank P < .001). After full adjustment, hazard ratios (95% confidence intervals) for all-cause mortality of T1, T2, and T3 were 0.637 (0.619-0.658), 0.482 (0.462-0.503), and 0.258 (0.244-0.272), respectively, in men and 0.608 (0.580-0.637), 0.406 (0.385-0.430), and 0.190 (0.178-0.203), respectively, in women. Similar inverse associations were observed across most major cancer types. In this nationwide cohort of Korean cancer survivors, statin prescription duration was associated with lower all-cause mortality. Given the observational design and the potential for residual confounding and immortal time bias, these findings should be interpreted cautiously.
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Kim et al. (2026) conducted a cohort in Cancer survivors (n=154,916). Statin prescription vs. Statin nonusers was evaluated on All-cause mortality (HR 0.258 (men, T3) and 0.190 (women, T3), 95% CI 0.244-0.272 (men) and 0.178-0.203 (women), p=<.001). Longer statin prescription duration was associated with lower all-cause mortality in cancer survivors, with the longest duration yielding HRs of 0.258 (95% CI 0.244-0.272) in men and 0.190 in women.
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