Key result
Long-term low-dose aspirin use in ischemic cardiac or cerebrovascular disease survivors was associated with a significantly reduced risk of primary cancer (aHR 0.42; 95% CI 0.38-0.45; P<0.0001).
Why the study?
Ischemic cardiac or cerebrovascular disease survivors face a high risk of cancer, but the association of long-term low-dose aspirin with primary cancer risk in this population required investigation.
Does long-term low-dose aspirin use reduce the risk of primary cancer in survivors of ischemic cardiac or cerebrovascular disease?
Cohort (n=48,060)
Does long-term low-dose aspirin use reduce the risk of primary cancer in survivors of ischemic cardiac or cerebrovascular disease?
Hazard Ratio: 0.42 (95% CI 0.38–0.45)
Absolute Event Rate: 6.49% vs 14.04%
p-value: p=<0.0001
Long-term low-dose aspirin use in survivors of ischemic cardiac or cerebrovascular disease is associated with a significantly reduced risk of primary cancer.
Long-term low-dose aspirin was associated with reduced primary cancer risk in ICCD survivors; leaves open a chemopreventive role pending randomized trials.
Ischemic cardiac or cerebrovascular disease (ICCD) survivors represent a subpopulation with a high cancer risk. Antiplatelet medications, such as aspirin, remain a fundamental therapy for the secondary prevention of ischemic attack in these patients. We conducted a population-based cohort study to investigate the association of long-term low-dose aspirin use with the risk of primary cancer in ICCD survivors. Patients aged ≥20 years with newly diagnosed ICCD (n = 98,519) between January 2000 and December 2013 were identified from the Taiwan National Health Insurance Research Database. The aspirin user and nonuser groups (each n = 24,030) were propensity-matched (1:1) for age, sex, comorbidities, prior medications, ICCD diagnosis year, and year of index dates. The incidence rate of primary cancer was significantly lower in the user group (6.49/1000 person-years) than in the nonuser group (14.04/1000 person-years). Multivariate Cox regression analysis indicated that aspirin use was an independent factor associated with a reduced risk of primary cancer (aHR (95% confidence interval) = 0.42 (0.38−0.45)) after adjustment. Kaplan−Meier curve analysis revealed that the cumulative incidence rate of primary cancer was significantly lower (p < 0.0001) in the user group than in the nonuser group over the 14-year follow-up period. Subgroup analyses demonstrated that this anticancer effect increased with duration of treatment and with similar estimates in women and men. In addition, aspirin use was associated with a reduced risk for seven out of the ten most common cancers in Taiwan. These findings suggest the anticancer effect of aspirin in ICCD survivors and provide information for assessing the benefit-to-risk profile of aspirin as an antiplatelet medication in these patients.
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Liao et al. (2022) conducted a cohort in Ischemic cardiac or cerebrovascular disease (ICCD) (n=48,060). Long-term low-dose aspirin vs. Nonusers was evaluated on Primary cancer (aHR 0.42, 95% CI 0.38-0.45, p=<0.0001). Long-term low-dose aspirin use in ischemic cardiac or cerebrovascular disease survivors was associated with a significantly reduced risk of primary cancer (aHR 0.42; 95% CI 0.38-0.45; P<0.0001).
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