Abstract

Identification of somatic mutations in ctDNA may detect minimal residual disease (MRD) in patients with curatively treated CRC who may eventually recur. Highly sensitive NGS-based assays are known to have comparable sensitivity to digital PCR approaches, with the added benefit of broader coverage and no requirement for a priori knowledge of tumour-based mutations. The ASpirin for Dukes C and high risk Dukes B COLorecTal cancer trial (ASCOLT, NCT00565708) is a randomised, double-blinded, phase III fully accrued study investigating the benefit and safety of aspirin in the adjuvant setting.

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