Effect of daily aspirin on long-term risk of death due to cancer: analysis of individual patient data from randomised trials
Abstract
Background Treatment with daily aspirin for 5 years or longer reduces subsequent risk of colorectal cancer. Several lines of evidence suggest that aspirin might also reduce risk of other cancers, particularly of the gastrointestinal tract, but proof in man is lacking. We studied deaths due to cancer during and after randomised trials of daily aspirin versus control done originally for prevention of vascular events. Methods We used individual patient data from all randomised trials of daily aspirin versus no aspirin with mean duration of scheduled trial treatment of 4 years or longer to determine the effect of allocation to aspirin on risk of cancer death in relation to scheduled duration of trial treatment for gastrointestinal and non-gastrointestinal cancers. In three large UK trials, long-term post-trial follow-up of individual patients was obtained from death certificates and cancer registries. Results In eight eligible trials (25 570 patients, 674 cancer deaths), allocation to aspirin reduced death due to cancer (pooled odds ratio [OR] 0·79, 95% CI 0·68-0·92, p=0·003). On analysis of individual patient data, which were available from seven trials (23 535 patients, 657 cancer deaths), benefit was apparent only after 5 years' follow-up (all cancers, hazard ratio [HR] 0·66, 0·50-0·87; gastrointestinal cancers, 0·46, 0·27-0·77; both p=0·003). The 20-year risk of cancer death (1634 deaths in 12 659 patients in three trials) remained lower in the aspirin groups than in the cont…
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Several meta-analyses of selected randomized trials of generally low-dose aspirin have suggested that aspirin use might reduce the risk of cancer-in particular gastrointestinal tract cancer-by up to one third during long-term follow-up, with effects becoming apparent approximately 3 years after randomization.
“Several meta-analyses of selected randomized trials of generally low-dose aspirin have suggested that aspirin use might reduce the risk of cancer - in particular, gastrointestinal tract cancer - by up to one third during long-term follow-up, with effects becoming apparent approximately 3 years after randomization.”
From Effects of aspirin for primary prevention in persons with diabetes mellitus (2018) · cites this paper as [24]
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- Authors
- Rothwell, P. M., Fowkes, F. G. R., Belch, J. F., Ogawa, H., Warlow, C. P., & Meade, T. W.
- Affiliations
- University of Oxford (GB)
- University of Edinburgh (GB)
- Kumamoto University (JP)
- Western General Hospital (GB)
- University of London (GB)
- Corresponding author
- Rothwell, Peter M
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 2011-01
- Volume
- 377
- Issue
- 9759
- Pages
- 31-41
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W2151036184
- Cited by
- 1,497
- References
- 4
- Citations by year
- 2026: 35 · 2025: 38 · 2024: 44 · 2023: 57 · 2022: 56 · 2021: 83 · 2020: 79 · 2019: 101 · 2018: 99 · 2017: 110 · 2016: 119 · 2015: 125 · 2014: 127 · 2013: 143 · 2012: 163
- FWCI
- 15.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- The Lancet (publishedVersion)
- PubMed (publishedVersion)
- Discovery Research Portal (University of Dundee) (submittedVersion)
- LSHTM Research Online (London School of Hygiene and Tropical Medicine) (submittedVersion)
- Funders
- National Institute for Health and Care Research (RP-PG-0606-1146)
- Topics
- Health Sciences › Medicine › Pharmacology › Inflammatory mediators and NSAID effects
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Antiplatelet Therapy and Cardiovascular Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- aspirin, cancer mortality, cancer prevention, gastrointestinal cancer, long-term follow-up, individual patient data, post-trial follow-up, esophageal cancer, colorectal cancer, pooled odds ratio, hazard ratio
- MeSH terms
- Aspirin, Drug Administration Schedule, Humans, Neoplasms, Survival Analysis, Randomized Controlled Trials as Topic, Cyclooxygenase 2 Inhibitors
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