Clinical Trials in France / NCT04935853
Recruiting
Observational
Prognostic and Predictive Markers of Response to Treatment in Patients With Bile Duct Cancer: ACABi PRONOBIL Study
NCT04935853 · tracked via the Priya Life Science France tracker
Condition(s) studied
Biliary Tract Cancer
Study summary
The objective of this study is to identify prognosis and predictive markers of response to treatments (surgery, chemotherapy, targeted therapy,loco-regional treatments ) in patients with bile duct cancer. The effectiveness and tolerance of these treatments in current practice will also be evaluated.
Eligibility
Inclusion Criteria:
* All locations of primitives (intrahepatic CCA, extrahepatic CCA, adenocarcinoma of the gallbladder; ampullomas excluded)
* Age \> 18 years
* Diagnosed between 2003 and 2030 (minimum follow-up 2 years)
* Written written non-opposition +/- signed informed consent for genetic studies (N.B.:
exemption requested for a deceased patient) N.B. Authorized inclusion in a therapeutic research protocol
Exclusion Criteria:
* Patient under guardianship, curatorship or legal protection
* Pregnant or breastfeeding women
* Any medical, psychological or social situation, which could prevent the compliance with the protocol according to the investigator's assessment
* Refusal to participate in the study
Primary outcome measure(s)
- Rate of patients with advanced bile duct cancer (BDC) experiencing overall survival (OS) less than 6 months — Up to 10 years from the date of initial cancer diagnosis (or until death if it occurs before 10 years)
Identification of clinical and tumor predictive factors of overall survival (OS) (prognostic markers) in patients with advanced bile duct cancer (BDC). OS defined as a period between the start of treatment and death, whatever the cause.
Trial sites (32)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU Hôpital Sud Amiens | Amiens | France | Recruiting |
| CHU Angers | Angers | France | Recruiting |
| CHU Besançon | Besançon | France | Recruiting |
| Hôpital Avicenne | Bobigny | France | Recruiting |
| CHU - Henri Mondor | Créteil | France | Recruiting |
| CHU Dijon | Dijon | France | Recruiting |
| CHU Grenoble | Grenoble | France | Recruiting |
| CHU Lille | Lille | France | Recruiting |
| Centre Léon Bérard | Lyon | France | Recruiting |
| Hôpital Croix Rousse | Lyon | France | Recruiting |
| Hôpital Edouard Herriot | Lyon | France | Recruiting |
| Hôpital Privé Jean Mermoz | Lyon | France | Recruiting |
| Institut Paoli Calmette | Marseille | France | Recruiting |
| CHU Saint Eloi Montpellier | Montpellier | France | Recruiting |
| CHR Orléans | Orléans | France | Recruiting |
| Groupe Hospitalier Pitié Salpêtrière | Paris | France | Recruiting |
| Hôpital Ambroise Paré | Paris | France | Recruiting |
| Hôpital Cochin | Paris | France | Recruiting |
| Hôpital Saint Antoine | Paris | France | Recruiting |
| Hôpital Saint Louis | Paris | France | Recruiting |
| Institut Mutualiste Montsouris | Paris | France | Recruiting |
| Hôpital Haut Lévêque | Pessac | France | Recruiting |
| CHU Poitiers | Potiers | France | Recruiting |
| Hôpital Robert Debré -CHU Reims | Reims | France | Recruiting |
| Centre Eugène Marquis | Rennes | France | Recruiting |
| CHU Rouen Charles Nicolle | Rouen | France | Recruiting |
| Institut Curie | Saint-Cloud | France | Recruiting |
| CHU Saint Etienne | Saint-Etienne | France | Recruiting |
| CHU Rangueil | Toulouse | France | Recruiting |
| CHU Tours | Tours | France | Recruiting |
| CHRU Nancy Site Brabois | Vandœuvre-lès-Nancy | France | Recruiting |
| Institut Gustave Roussy | Villejuif | France | Recruiting |
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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 NCT04935853 on ClinicalTrials.gov ↗ ← All trials in France