Key result
Post-diagnostic aspirin initiation is linked to ~46% higher prostate cancer mortality.
Why the study?
The association between the use of aspirin and mortality in patients with prostate cancer remains uncertain.
Does post-diagnostic aspirin use reduce prostate cancer mortality and all cause mortality in men with nonmetastatic prostate cancer?
Cohort (n=11,779)
Yes
Does post-diagnostic aspirin use reduce prostate cancer mortality and all cause mortality in men with nonmetastatic prostate cancer?
Hazard Ratio: 1.46 (95% CI 1.29–1.65)
Initiating aspirin after a prostate cancer diagnosis is associated with increased mortality, though this is likely a noncausal association driven by confounding by indication.
No change to aspirin management warranted; leaves open confounding by indication in this observational association.
PURPOSE: The association between the use of aspirin and mortality in patients with prostate cancer remains uncertain. We determine whether the use of aspirin in patients with prostate cancer is associated with a decreased risk of prostate cancer mortality and all cause mortality. MATERIALS AND METHODS: Using the United Kingdom National Cancer Data Repository, Clinical Practice Research Datalink and associated databases, we identified a cohort of men with nonmetastatic prostate cancer between 1998 and 2009, followed until 2012. Cox proportional hazards models were used to estimate adjusted HRs with 95% CIs of mortality outcomes associated with post-diagnostic use of aspirin defined as a time-varying exposure. Effect modification by pre-diagnostic aspirin use was also assessed. RESULTS: The cohort included 11,779 men followed for 5.4 years (SD 2.9). Post-diagnostic aspirin use was associated with an increased risk of prostate cancer mortality (HR 1.46, 95% CI 1.29-1.65) and all cause mortality (HR 1.37, 95% CI 1.26-1.50). These increased risks were restricted to patients initiating aspirin after the prostate cancer diagnosis (HR 1.84, 95% CI 1.59-2.12, and HR 1.70, 95% CI 1.53-1.88, respectively), and not in patients who were already exposed to aspirin before the diagnosis (HR 0.97, 95% CI 0.81-1.16 and HR 0.98, 95% CI 0.87-1.18, respectively). CONCLUSIONS: The post-diagnostic use of aspirin is not associated with a decreased risk of prostate cancer outcomes. Increased risks were restricted to patients initiating these drugs after their diagnosis, suggesting a noncausal association.
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Assayag et al. (2014) conducted a cohort in nonmetastatic prostate cancer (n=11,779). Post-diagnostic aspirin use vs. No post-diagnostic aspirin use was evaluated on Prostate cancer mortality (HR 1.46, 95% CI 1.29-1.65). Post-diagnostic aspirin use was associated with an increased risk of prostate cancer mortality (HR 1.46; 95% CI 1.29-1.65), which was restricted to patients initiating aspirin after diagnosis.
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