Identifying markers to predict treatment response in bile duct cancer
Official title: Marqueurs Pronostiques et prédictifs de réponse Aux Traitements Chez Les Patients Atteints de Cancer Des Voies Biliaires : Cohorte Multicentrique ACABi PRONOBIL
Run by GERCOR - Multidisciplinary Oncology Cooperative Group · NCT04935853 · Data updated 2026-11-12
This study is trying to find markers that can help doctors predict how well different treatments will work for people with bile duct cancer.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1350 (estimated) |
| Sponsor | GERCOR - Multidisciplinary Oncology Cooperative Group Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 32 sites (Amiens and 31 other locations) |
| Status | Recruiting |
| Started | May 23, 2022 |
| Main results expected | June 1, 2030 |
| Study ends | June 1, 2040 |
| Registry record updated | July 23, 2025 |
| Trial ID | NCT04935853 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults over 18 years old diagnosed with any form of bile duct cancer between 2003 and 2030.
✕Probably not a fit
Patients who are under guardianship, pregnant, breastfeeding, or unable to comply with the study protocol may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to identify prognostic and predictive markers that can help determine how patients with bile duct cancer respond to various treatments, including surgery, chemotherapy, and targeted therapies. It is a multi-center, cohort study that will collect data from patients diagnosed between 2003 and 2030, with a follow-up period of 10 years from the initial diagnosis. The study will evaluate the effectiveness and tolerance of current treatment practices and will include both retrospective and prospective data collection methods.
Why it matters
Potential benefit: If successful, this study could lead to more personalized treatment strategies for patients with bile duct cancer, improving their outcomes.
How similar studies have gone: Other studies have shown promise in identifying predictive markers for cancer treatment responses, making this approach both relevant and potentially impactful.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
-
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
Show 26 more locations
-
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
Study contacts
- Principal investigator: Cindy Neuzillet, Dr — Institut Curie, Saint-Cloud
- Study coordinator: Cindy Neuzillet, Dr
- Email: cindy.neuzillet@curie.fr
- Phone: +33 (0)1 47 11 15 15
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Sintilimab with NALIRIFOX or GP as first-line treatment for metastatic biliary tract cancer
This study tests whether adding sintilimab to either NALIRIFOX or gemcitabine‑cisplatin can help people with metastatic biliary tract cancer who have not had prior systemic therapy.
-
ABBV-253 in adults with advanced solid tumors
This study tests ABBV-253 to see if it is safe, how it affects the cancer, and how the drug moves in the body for adults with advanced solid tumors.
-
Liposomal irinotecan with 5-FU/LV and sintilimab plus SBRT for unresectable biliary tract cancer
This trial tests whether combining liposomal irinotecan, 5-FU/LV, and sintilimab, followed by SBRT, can help patients with unresectable locally advanced biliary tract cancer become eligible for surgery or slow disease progression.
-
Futibatinib and immunotherapy with chemo as first-line treatment for advanced biliary tract cancer
A first-line treatment test combines Futibatinib with Zimberelimab and Gemcitabine/Cisplatin to see if it improves survival in people with unresectable or advanced biliary tract cancer.
-
ctDNA-guided precision care for lung, GIST, colorectal, biliary, and ovarian cancers
This trial tests a blood test that looks for tumor DNA in patients with several cancers to help guide personalized treatment decisions.
-
Dual-target HER2/CEA CAR-NK Cells in Advanced Biliary Tract Cancer
This trial tests a ready-to-use CAR-NK cell therapy that targets HER2 and CEACAM5 in adults with unresectable or metastatic biliary tract cancers after standard therapy to see if it can help control the disease.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.