Daily Aspirin Use and Prostate Cancer–Specific Mortality in a Large Cohort of Men with Nonmetastatic Prostate Cancer
- Eric J. Jacobs⇑,
- Christina C. Newton,
- Victoria L. Stevens,
- Peter T. Campbell,
- Stephen J. Freedland and
- Susan M. Gapstur
+ Author Affiliations
- Corresponding author: Eric J. Jacobs, PhD, Epidemiology Research Program, American Cancer Society, National Home Office, 250 Williams St, Atlanta GA, 30303-1002; e-mail: Eric.Jacobs@cancer.org.
Abstract
Purpose In a recent
analysis of a large clinical database, postdiagnosis aspirin use was
associated with 57% lower prostate cancer–specific
mortality (PCSM) among men diagnosed with
nonmetastatic prostate cancer. However, information on this association
remains
limited. We assessed the association between
daily aspirin use and PCSM in a large prospective cohort.
Patients and Methods
This analysis included men diagnosed with nonmetastatic prostate cancer
between enrollment in the Cancer Prevention Study-II
Nutrition Cohort in 1992 or 1993 and June 2009.
Aspirin use was reported at enrollment, in 1997, and every 2 years
thereafter.
During follow-up through 2010, there were 441
prostate cancer deaths among 8,427 prostate cancer cases with
information on
prediagnosis aspirin use and 301 prostate cancer
deaths among 7,118 prostate cancer cases with information on
postdiagnosis
aspirin use.
Results Compared with
no aspirin use, neither prediagnosis nor postdiagnosis daily aspirin use
were statistically significantly associated
with PCSM (prediagnosis use,
multivariable-adjusted hazard ratio (HR) = 0.92, 95% CI 0.72 to 1.17,
postdiagnosis use, HR =
0.98; 95% CI, 0.74 to 1.29). However, among men
diagnosed with high-risk cancers (≥ T3 and/or Gleason score ≥ 8),
postdiagnosis
daily aspirin use was associated with lower PCSM
(HR = 0.60; 95% CI, 0.37 to 0.97), with no clear difference by dose
(low-dose,
typically 81 mg per day, HR = 0.50; 95% CI, 0.27
to 0.92, higher dose, HR = 0.73; 95% CI, 0.40 to 1.34).
Conclusion A
randomized trial of aspirin among men diagnosed with nonmetastatic
prostate cancer was recently funded. Our results suggest
any additional randomized trials addressing this
question should prioritize enrolling men with high-risk cancers and
need
not use high doses.
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