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Spots Global Cancer Trial Database for Prognostic and Predictive Markers of Response to Treatment in Patients With Bile Duct Cancer: ACABi PRONOBIL Study

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Trial Identification

Brief Title: Prognostic and Predictive Markers of Response to Treatment in Patients With Bile Duct Cancer: ACABi PRONOBIL Study

Official Title: Marqueurs Pronostiques et prédictifs de réponse Aux Traitements Chez Les Patients Atteints de Cancer Des Voies Biliaires : Cohorte Multicentrique ACABi PRONOBIL

Study ID: NCT04935853

Interventions

Study Description

Brief 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.

Detailed Description: Bile duct cancers are a heterogeneous group of rare tumors with a poor prognosis. Surgery is the only curative modality for localized forms. Chemotherapy is the standard treatment in advanced forms. Identification of prognostic and predictive markers to better stratify patients and to guide therapeutic decisions is a major issue. It is retro-prospective (diagnosis between 2003 and 2021) and prospective (diagnosis between 2021 and 2030) multi-center, cohort study. Follow-up for 10 years from initial cancer diagnosis will be done. Follow-up is retrospective only for patients operated on or diagnosed in the past for more than 10 years, and retro-prospective for operated patients or diagnosed in the past for less than 10 years. The data collected for each patient are available during the life cycle of this clinical trial to fulfil an educational requirement (e.g. a doctoral thesis) upon request and authorization from the study committee and the study sponsor (GERCOR).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

CHU Hôpital Sud Amiens, Amiens, , France

CHU Angers, Angers, , France

CHU Besançon, Besançon, , France

Hôpital Avicenne, Bobigny, , France

CHU - Henri Mondor, Créteil, , France

CHU Dijon, Dijon, , France

CHU Grenoble, Grenoble, , France

CHU Lille, Lille, , France

Centre Léon Bérard, Lyon, , France

Hôpital Croix Rousse, Lyon, , France

Hôpital Edouard Herriot, Lyon, , France

Hôpital Privé Jean Mermoz, Lyon, , France

Institut Paoli Calmette, Marseille, , France

CHU Saint Eloi Montpellier, Montpellier, , France

CHU Nantes, Nantes, , France

Centre Antoine Lacassagne, Nice, , France

CHR Orléans, Orléans, , France

Groupe Hospitalier Pitié Salpêtrière, Paris, , France

Hôpital Ambroise Paré, Paris, , France

Hôpital Cochin, Paris, , France

Hôpital Saint Antoine, Paris, , France

Hôpital Saint Louis, Paris, , France

Institut Mutualiste Montsouris, Paris, , France

Hôpital Haut Lévêque, Pessac, , France

CHU Poitiers, Potiers, , France

Hôpital Robert Debré -CHU Reims, Reims, , France

Centre Eugène Marquis, Rennes, , France

CHU Rouen Charles Nicolle, Rouen, , France

Institut Curie, Saint-Cloud, , France

CHU Saint Etienne, Saint-Étienne, , France

CHU Rangueil, Toulouse, , France

CHU Tours, Tours, , France

CHRU Nancy Site Brabois, Vandœuvre-lès-Nancy, , France

Institut Gustave Roussy, Villejuif, , France

Contact Details

Name: Cindy Neuzillet, Dr

Affiliation: Institut Curie, Saint-Cloud

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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