Abstract

IntroductionRecent observational studies indicate that post-diagnostic use of aspirin in breast cancer patients may protect against cancer progression perhaps by inhibiting cyclooxygenase-2 dependent mechanisms. Evidence also supports a crucial role for interactions between tumour cells and circulating platelets in cancer growth and dissemination, therefore, use of low-dose aspirin may reduce the risk of death from cancer in breast cancer patients.MethodsA cohort of newly diagnosed breast cancer patients (1998 to 2006) were identified in the UK Clinical Practice Research Datalink (and confirmed by cancer registry linkage). Cancer-specific deaths were identified up to 2011 from Office for National Statistics mortality data. A nested case-control analysis was conducted using conditional logistic regression to compare post-diagnostic aspirin exposure using General Practice prescription data in 1,435 cases (breast cancer deaths) with 5,697 controls (matched by age and year of diagnosis).ResultsAfter breast cancer diagnosis, 18.3% of cancer-specific deaths and 18.5% of matched controls received at least one prescription for low-dose aspirin, corresponding to an odds ratio (OR) of 0.98 (95% CI 0.83, 1.15). Adjustment for potential confounders (including stage and grade) had little impact on this estimate. No dose response relationship was observed when the number of tablets was investigated and no associations were seen when analyses were stratified by receipt of prescriptions for aspirin in the pre-diagnostic period, by stage at diagnosis or by receipt of prescriptions for hormone therapy.ConclusionsOverall, in this large population-based cohort of breast cancer patients, there was little evidence of an association between receipt of post-diagnostic prescriptions for low-dose aspirin and breast cancer-specific death. However, information was not available on medication compliance or over-the-counter use of aspirin, which may have contributed to the null findings.

Highlights

  • Recent observational studies indicate that post-diagnostic use of aspirin in breast cancer patients may protect against cancer progression perhaps by inhibiting cyclooxygenase-2 dependent mechanisms

  • We investigated the association between post-diagnostic aspirin exposure and breast cancer-specific mortality in a large cancer registry defined population-based cohort of breast cancer patients in the United Kingdom (UK), in whom aspirin exposure was determined from prescription records

  • Patient cohort Overall, there were 11,863 primary breast cancers diagnosed between 1998 and 2007 identified in National Cancer Data Repository (NCDR), with no previous record of cancer, that were linked to Clinical Practice Research Datalink (CPRD)

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Summary

Introduction

Recent observational studies indicate that post-diagnostic use of aspirin in breast cancer patients may protect against cancer progression perhaps by inhibiting cyclooxygenase-2 dependent mechanisms. Evidence supports a crucial role for interactions between tumour cells and circulating platelets in cancer growth and dissemination, use of low-dose aspirin may reduce the risk of death from cancer in breast cancer patients. Evidence is accumulating that aspirin may protect against the development of some cancers, including breast cancer; for example, meta-analyses of observational studies indicate that breast cancer risk is reduced by 10 to 15% among aspirin users [1,2]. A growing body of evidence supports a crucial but complex role for interactions between tumour cells and circulating platelets in cancer growth and dissemination [9,10]. It is possible that the antiplatelet activity of (low-dose) aspirin may reduce the risk of metastasis in cancer patients by, for example, preventing angiogenesis or tumour cell extravasation and tissue invasion [10,11]

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