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technologiesTechnologyPhase 3

Aspirin for cancer prevention and adjuvant therapy

Daily low-dose aspirin lowers bowel cancer risk in people with Lynch syndrome and appears to cut recurrence in bowel cancers with a particular mutation. In healthy older people it caused more harm than good.

Long-term aspirin reduces colorectal cancer incidence and mortality in pooled analyses of cardiovascular trials with 20-year follow-up, and in CAPP2 halved colorectal cancer in Lynch syndrome carriers (600 mg/day, 10-year follow-up); the US Preventive Services Task Force nonetheless withdrew its general recommendation in 2022 because ASPREE (NEJM 2018) found more cancer deaths (HR 1.31) and no cancer prevention in healthy adults aged 70 and over. In the adjuvant setting the biomarker-directed ALASCCA trial (NEJM 2025) showed that 160 mg aspirin for three years roughly halved recurrence in resected colorectal cancer with PIK3CA or other PI3K-pathway alterations, and the 11,000-patient ADD-ASPIRIN trial across breast, colorectal, gastro-oesophageal and prostate cancers continues. Aspirin is the model repurposed generic: cheap, mechanistically plausible, and requiring publicly funded trials because no company will run them.

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How it works

COX-1/COX-2 inhibition reduces prostaglandin E2-driven proliferation and inflammation and blunts platelet cloaking of circulating tumour cells; PI3K-pathway-mutant tumours depend on PTGS2 signalling and are selectively sensitive.

Strengths
  • Randomised evidence in Lynch syndrome and PIK3CA-altered colorectal cancer
  • Pennies per day, universally available
  • Biomarker allows targeting
Limitations
  • Bleeding harm and excess cancer deaths in older unselected adults
  • Effect emerges only after years
  • Implementation of ALASCCA requires routine PIK3CA testing

Latest papers

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