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Active, not recruiting Observational

Evaluation of an Early Radiomic Signature in Patients With Metastatic Pancreatic Adenocarcinoma Treated With First-line Chemotherapy

NCT07243288 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-01-09
Last updated
2025-11-21

Condition(s) studied

Pancreatic CancerMeSH Term-Pancreatic Cancer, Adult)

Investigational drug(s) / intervention(s)

Patients treated with FOLFOX or FOLFIRINOX in first linePatients treated with GEMCITABINE in first line

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients (≥18 years) * Diagnosis of acute alcoholic hepatitis (ICD10 C25) in a pathology report, followed by manual verification in clinical documents Exclusion Criteria: * Patients younger than 18 years at diagnosis

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)

FacilityCityRegionStatus
Hôpital Cochin Paris France
Official registry record

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