Daily Aspirin May Reduce Risk of Cancer Death
Design
Analysis of individual patient data from 8 trials in which aspirin (doses ranged from 75–1,200 mg daily) was the interventional treatment used in cardiovascular risk reduction trials. None of the trials was designed to assess cancer incidence or deaths due to cancer. Trials were identified using public databases. All trials were randomized and had a mean scheduled treatment period of at least four years or more. Randomized allocation included aspirin versus no aspirin (no placebo given) or aspirin versus no aspirin in the presence of another antiplatelet or antithrombolytic agent (e.g., warfarin). Long-term (20-year) data was available for 3 trials using the United Kingdom’s national death certification and cancer registration systems.
Key Findings
Pooled analysis of 8 trials of aspirin showed a significant reduction in deaths due to cancer (674 deaths in 25,570 patients; OR 0.79, CI 0.68–0.92, P=0.003). Individual data available for 7 of the trials showed benefit was apparent only after 5 years’ follow-up (all cancers’ HR 0.66, CI 0.5–0.87; GI cancers HR=0.46, CI 0.27–0.77; P=0.003 for both sets of data). This latent effect was 5 years for esophageal, pancreatic, brain, and lung cancers. An even longer latency for measurable reduction in deaths was found for stomach, colorectal, and prostate cancers. The effect of aspirin was largely limited to adenocarcinomas. The benefit of aspirin was not related to the dose taken, gender, or smoking status. Benefit did appear to increase with age and duration of aspirin intervention used in the trial.
Practice Implications
Many publications have suggested a protective role of aspirin intake on cancers of the colon, stomach, and esophagus. This is the first publication that shows a significant reduction of overall cancer deaths. In addition to the strong evidence for protective effects against gastrointestinal cancers, there is supportive evidence from several observation studies of a reduction in the incidence of prostate, ovarian, lung, and brain cancers as well. The above publication found that deaths due to cancers overall was reduced by 20% for those using aspirin long-term, and upwards of 35% for lower gastrointestinal cancers specifically. This is compelling outcome data on the use of an inexpensive, relatively safe intervention.
There are a few salient points in this study that are useful to keep in mind for clinicians. First, the benefit of aspirin did not correlate with the dosage used, so that a minimum dose of 75 mg is expected to be sufficient to confer benefit. Second, the benefit of aspirin was a latent effect, with reductions in deaths beginning after 5 years of follow up. Third, the reduction in deaths correlated with the duration of aspirin consumption, with longer aspirin intervention correlating with greater benefit. There was no benefit seen in those who took aspirin for less than 5 years. Last, reduction in deaths was found for individuals with adenocarcinoma specifically, not other histological types.