Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Colorectal cancer is the third most common cancer in men, and the second most common in women. Screening for colorectal cancer is based on the search for blood in the stool using fecal immunochemical test (FIT). Occult bleeding is an indication for colonoscopy. In a FIT positive population, 60% of colonoscopies are negative, 34% diagnose an adenomatous lesion, and 6% a cancer. The identification of new biological markers could reduce the number of colonoscopies performed. Cancer cells release extracellular vesicles that contain proteins, mRNAs, DNA, which they can transfer to neighbouring or distant cells. The use of exosomal proteins as novel tumor markers looks very promising. We performed a pilot study comparing the levels of different exosomal proteins in 74 subjects which was recently accepted for publication in Journal of Clinical Laboratory Analysis. Comparison of results showed that only matrix metalloproteinase 14 (MMP14) was significantly higher in patients with colorectal cancer or adenoma than in people with normal colonoscopy.
The primary objective of the current study is to determine the best cut-off value of MMP-14 for colorectal cancer screening and to evaluate the performance (Sensitivity, Specificity…) associated to this cut-off value. The secondary objective will be to determine the best cut-off value of MMP-14 for colorectal adenomas screening and to evaluate its performance.
For this purpose, 650 patients, seen for diagnostic colonoscopy following a positive FIT test, will be included in the study. After blood collection and exosome isolation, MMP-14 will be measured using a quantitative test (enzyme-linked immunosorbent assay) and the results will be associated with colonoscopy results to determine the sensitivity, specificity, positive predictive value (PPV) and net present value (NPV).
Inclusion criteria: Individuals presenting for colonoscopy with a positive FIT result.
Non-inclusion criteria:
Once consent has been signed and the patient has been included in the study, blood will be drawn from 2 additional tubes of 5 ml each, either in the consultation room or in the operating room, when the infusion is set up for colonoscopy under general anaesthetic. Plasma will be collected at the various participating facilities (2 x 5mL EDTA tubes), centrifuged at 1000g for 10 minutes, then frozen at -80°C. Samples will then be sent to the Reims University Hospital Biology Department for storage before analysis.
The isolation of exosomes from the patient's plasma and their characterization: size, number (determined using the Malvern Panalytical NanoSight NS300), and MMP14 concentration (determined by enzyme-linked immunosorbent assay), will be carried out at the CNRS UMR7369 "Matrice Extracellulaire et Dynamique Cellulaire (MEDyC)" unit at the University of Reims Champagne Ardenne.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Serum Matrix Metalloproteinase (MMP14) | Experimental | Blood will be drawn from 2 additional tubes of 5 ml each, either in the consultation room or in the operating room. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Blood will be drawn from 2 additional tubes of 5 ml each | Other | Blood will be drawn from 2 additional tubes of 5 ml each |
|
| Measure | Description | Time Frame |
|---|---|---|
| Serum Matrix Metalloproteinase (MMP14) : normal versus a cancerous lesion | Concentration of Serum Matrix Metalloproteinase (MMP14) depending on whether the colonoscopy was normal or revealed a cancerous lesion | At 30 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Serum Matrix Metalloproteinase (MMP14) MMP14 Concentration: Normal vs. Adenoma | Concentration of Serum Matrix Metalloproteinase (MMP14) depending on whether the colonoscopy was normal or revealed an adenoma | At 30 minutes |
| Serum MMP14 Concentration according to adenoma characteristics |
Not provided
Inclusion criteria:
Exclusion criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Laurent RAMONT | Contact | 03 26 78 78 01 | 0033 | lramont@chu-reims.fr |
| Olivier BOUCHE | Contact | 03 26 78 31 13 | obouche@chu-reims.fr |
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Damien JOLLY | Recruiting | Reims | France |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Concentration of Serum Matrix Metalloproteinase (MMP14) according to adenoma characteristics |
| At 30 minutes |
| Serum MMP14 Concentration between groups: normal colonoscopy vs. adenoma and cancerous lesions | Comparison of exosomal plasma MMP14 concentration between groups: normal colonoscopy vs. adenoma and cancerous lesions | At 30 minutes |
| Diagnostic performances of Serum MMP14 | Sensitivity and specificity | At 30 minutes |
| Concentration of markers derived from circulating tumor exosomes in the context of colorectal cancer | Mean value of markers derived from circulating tumor exosomes | At 30 minutes |