About this trial
This is an multicenter study that will test the diagnostic accuracy of a blood test (i.e., a liquid biopsy) for the diagnosis of colorectal cancer (CRC), advanced adenomas (AAs), as well as Lynch-syndrome associated cancers. Additionally, a pre-planned analysis will evaluate the use of this liquid biopsy as a tool for molecular residual disease monitoring purposes.
Eligibility criteria
Qualifiers
All individuals included in the study need to have had a colonoscopy at the time of blood sampling.
Received standard diagnostic and staging (as necessary) procedures as per local guidelines, and at least one sample was drawn before receiving any curative-intent treatment.
Received standard pathological and endoscopic diagnosis and assessment for cohort assignment
Disqualifiers
Lack of informed consent
Inflammatory bowel disease
Trial design
Treatments tested in this trial
- BEACON
Treatment groups
7
Treatment groupsSee each treatment group below.