About this trial
Early colorectal cancer screening increasingly detects small superficial colonic lesions, but current diagnostic tools still struggle to distinguish benign from malignant lesions and to assess lymph node risk. As histology after resection has limited accuracy, many patients undergo unnecessary surgery.
Liquid biopsy, analyzing circulating biomarkers such as tumor DNA, extracellular vesicles, and nucleosomes, offers a non-invasive way to better classify these lesions. Emerging evidence suggests it may outperform current criteria for predicting lymph node involvement in T1 colorectal cancer.
This study will establish a biobank of 1,000 patients to identify blood-based signatures that predict tumor stage and lymph node status. The hypothesis of the study is that circulating biomarkers can accurately differentiate benign from malignant lesions and identify patients with or without lymph node metastasis.
Eligibility criteria
Qualifiers
Patient of legal age (≥ 18 years)
Patient with a superficial colonic tumor refered for submucosal dissection
Patient included in the FECCo cohort (patients will be included concomitantly in FECCO-Biobank)
Patient wishing to participate in the FECCO-BioBank biological collection
Disqualifiers
Person with significant comorbidities preventing blood sampling
Patients with a distant metastasis detected by imaging
Person unable to read and write French
Person who have expressed their opposition to participating in this research after being informed by an investigator and having read the information sheet
Trial design
Treatments tested in this trial
- Venous blood sampling
Treatment groups
Sponsors and collaborators
University Hospital, Montpellier
Lead sponsor
University Hospital, Limoges
Collaborator
Société Nationale Française de Gastroentérologie
Collaborator