Cancer Colorectal
Conditions
Keywords
Oncology, Biology
Brief summary
Multicenter, inter-regional, case-control study with the primary objective of evaluating the discriminative power of the blood biomarker TFPI-1 to separate patients with histologically proven CRC from an asymptomatic control population between 50 and 75 years of age with normal colonoscopy.
Interventions
None listed
Sponsors
University Hospital, Lille
Ministry of Health, France
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Patients with suspected colorectal cancer for which colonoscopy is indicated. * Patients between 50 and 75 years old, asymptomatic from the digestive point of view (for example referred for colonoscopy as part of a pre-operative check-up of an inguinal hernia or 3 months after an episode of complicated sigmoiditis), for whom a follow-up colonoscopy is indicated. Note. * If the post-inclusion colonoscopy is normal, no biopsy will be performed and patients will be assigned to the control group. * If the colonoscopy performed after inclusion is abnormal (presence of at least one mucosal lesion), patients will be assigned to the "colorectal cancer" group or to the "polyps" group depending on the results of the anatomopathological analysis of the lesion(s)
Exclusion criteria
* All clinical situations outside of CRC that could increase TFPI-1 or 2 blood levels: acute coronary syndrome (unstable angina, acute myocardial infarction), severe sepsis, decompensated cirrhosis, pregnancy, chronic inflammatory bowel disease (Crohn's or ulcerative colitis), colitis or radiation rectitis. * Endoscopic polypectomy without prior histological confirmation. * Emergency (occlusion or peritonitis) * Minor patients. * Persons of full age under legal protection or unable to express their consent * Persons not affiliated to a social security system or beneficiaries of such a system. * Pregnant women, women in labor or nursing mothers.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Area under the ROC curve (AUC) of the TFPI-1 biomarker | At 2 months | the AUC of the TFPI-1 biomarker to separate the 2 groups (CRC+ and control, i.e., asymptomatic population between 50 and 75 years with normal colonoscopy). |
Secondary
| Measure | Time frame |
|---|---|
| AUC of the TFPI-2 biomarker to separate the 2 groups (CRC+ and control). | At 2 months |
| AUC of the discriminant score constructed by logistic regression with the 2 blood biomarkers as explanatory variables and the group type (CRC+ and control) as the variable to be explained. | At 2 months |
| Extension of c-index to the 3-group case proposed by Van Calster B et al. | At 2 months |
Countries
France
Contacts
CONTACTPhilippe ZERBIB, MD,PhD
PRINCIPAL_INVESTIGATORPhilippe ZERBIB, MD,PhD
University Hospital, Lille
Outcome results
None listed