Evaluation of an Early Radiomic Signature in Patients With Metastatic Pancreatic Adenocarcinoma Treated With First-line Chemotherapy
Condition(s) studied
Investigational drug(s) / intervention(s)
Patients treated with FOLFOX or FOLFIRINOX in first line: Treatment with FOLFOX or FOLFIRINOX (chemotherapy protocols) in first line
Patients treated with GEMCITABINE in first line: Treatment with GEMCITABINE (chemotherapy protocols) in first line
Study summary
Pancreatic cancer, which has a poor prognosis, is becoming increasingly common in industrialized countries. Chemotherapy is the main treatment available for metastatic disease. Response to chemotherapy is currently assessed using imaging to monitor changes in the size of lesions undergoing treatment. Radiomics is a new method of analyzing quantitative data extracted from imaging that can be used to develop prediction algorithms and evaluate response to treatment. There is little robust radiomics data available for evaluating response to first-line treatments for pancreatic adenocarcinoma. Our main hypothesis is that quantifying tumor-related architectural changes could enable early identification of patients who will not respond to chemotherapy.
Eligibility
Primary outcome measure(s)
- Overall survival after diagnosis of pancreatic cancer — From diagnosis up to 7 years after
Overall survival will be assessed using mortality data recorded in the AP-HP Clinical Data Warehouse. The objective is to evaluate prognosis and identify risk factors associated with death after a diagnosis of pancreatic cancer, by integrating clinical, biological, histological and radiomics information. Survival will be analysed at multiple time points, including 1 month, 6 months, and 1 year after diagnosis.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Hôpital Cochin | Paris | France |
More Assistance Publique - Hôpitaux de Paris trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07243288 on ClinicalTrials.gov ↗ ← All trials in France