ADD-ASPIRIN: A phase III, double-blind, placebo controlled, randomised trial assessing the effects of aspirin on disease recurrence and survival after primary therapy in common non-metastatic solid tumours

Coyle, C. et al. (2016) ADD-ASPIRIN: A phase III, double-blind, placebo controlled, randomised trial assessing the effects of aspirin on disease recurrence and survival after primary therapy in common non-metastatic solid tumours. Contemporary Clinical Trials, 51, pp. 56-64. (doi: 10.1016/j.cct.2016.10.004) (PMID:27777129) (PMCID:PMC5127874)

Abstract

Background: There is a considerable body of pre-clinical, epidemiological and randomised data to support the hypothesis that aspirin has the potential to be an effective adjuvant cancer therapy. Methods: Add-Aspirin is a phase III, multi-centre, double-blind, placebo-controlled randomised trial with four parallel cohorts. Patients who have undergone potentially curative treatment for breast (n = 3100), colorectal (n = 2600), gastro-oesophageal (n = 2100) or prostate cancer (n = 2120) are registered into four tumour specific cohorts. All cohorts recruit in the United Kingdom, with the breast and gastro-oesophageal cohort also recruiting in India. Eligible participants first undertake an active run-in period where 100 mg aspirin is taken daily for approximately eight weeks. Participants who are able to adhere and tolerate aspirin then undergo a double-blind randomisation and are allocated in a 1:1:1 ratio to either 100 mg aspirin, 300 mg aspirin or a matched placebo to be taken daily for at least five years. Those participants ≥ 75 years old are only randomised to 100 mg aspirin or placebo due to increased toxicity risk. Results: The primary outcome measures are invasive disease-free survival for the breast cohort, disease-free survival for the colorectal cohort, overall survival for the gastro-oesophageal cohort, and biochemical recurrence-free survival for the prostate cohort, with a co-primary outcome of overall survival across all cohorts. Secondary outcomes include adherence, toxicity including serious haemorrhage, cardiovascular events and some cohort specific measures. Conclusions: The Add-Aspirin trial investigates whether regular aspirin use after standard therapy prevents recurrence and prolongs survival in participants with four non-metastatic common solid tumours.

• Item Type: Articles
• Additional Information: The Add-Aspirin trial is jointly funded by Cancer Research UK (CRUK) (grant number C471/A15015) and the National Institute Health Research (NIHR) Health Technology Assessment Programme (HTA) (project number 12/01/38). Bayer Pharmaceuticals AG has agreed to provide the Investigational Medicinal Products (IMPs). In India, the Sir Dorabji Tata Trust provides funding, and CIPLA Ltd. is providing supplies of aspirin 100 mg for the run-in period. The Add-Aspirin translational sample collection is funded by CRUK (C471/A19252). The trial is coordinated and supported by the Medical Research Council Clinical Trials Unit at University College London (MRC CTU at UCL).
• Status: Published
• Refereed: Yes
• Glasgow Author(s) Enlighten ID: Wilson, Professor Richard
• Authors: Coyle, C., Cafferty, F. H., Rowley, S., MacKenzie, M., Berkman, L., Gupta, S., Pramesh, C.S., Gilbert, D., Kynaston, H., Cameron, D., Wilson, R. H., Ring, A., and Langley, R. E.
• College/School: College of Medical Veterinary and Life Sciences > School of Cancer Sciences
• Journal Name: Contemporary Clinical Trials
• Publisher: Elsevier
• ISSN: 1551-7144
• ISSN (Online): 1551-7144
• Published Online: 21 October 2016
• Copyright Holders: Copyright © 2016 The Authors
• First Published: First published in Contemporary Clinical Trials 51:56-64
• Publisher Policy: Reproduced under a Creative Commons License