Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06705335

Convertases and Pancreatic Cancer: Cohort of Patients Treated for Pancreatic Adenocarcinoma

Convertases and Pancreatic Cancer. New Therapeutic and Prognostic Approach: Cohort of Patients Treated for Pancreatic Adenocarcinoma (CONVERCAP)

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Institut Bergonié · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, single-centre, observational study. The analysis of samples of pancreatic tumours and/or metastases taken during biopsy or surgery will lead to the determination of the level of expression of convertases in patients with pancreatic cancer and could be used as an additional prognostic means reinforcing those currently used.

Detailed description

After checking the inclusion criteria and signing the consent form, patients will be pre-selected for the study. A tumour sample (primary tumour or metastasis) will be taken either during a biopsy or during pancreatic or metastasis surgery. A blood sample will be taken on the same day as the tumour sample. The inclusion visit will be carried out by the investigating physician and will correspond to the visit when the results of the biopsy or surgery are reported. Inclusion of the patient will be possible if the tumour sample has been taken, is available, contributory and malignant (diagnosis or confirmation of pancreatic adenocarcinoma) and if the blood sample has been taken and is available. The patient will be considered to have failed pre-selection if * the tumour sample has not been taken or is not available, or * the tumour sample/histological result is non-contributory, or * the histological result is benign, or * the blood sample was not taken or is not available, or * the patient refuses to continue the study, or * the patient has withdrawn consent, or * any other reason preventing inclusion of the patient. Included patients will be treated and followed as usual, with standard radiological follow-up. For two years after inclusion, the tumour status (first progression) and vital status of the patient (alive, dead or lost to follow-up at the date of the visit) will be collected.

Conditions

Interventions

TypeNameDescription
OTHERBlood sampleOn the same day as the tumour sample is taken (biopsy or surgery), a blood sample of approximately 15 to 20 mL is taken in EDTA-free tubes.

Timeline

Start date
2026-01-01
Primary completion
2028-01-01
Completion
2029-01-01
First posted
2024-11-26
Last updated
2025-10-02

Source: ClinicalTrials.gov record NCT06705335. Inclusion in this directory is not an endorsement.