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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGERCOR - Multidisciplinary Oncology Cooperative Group

About this trial

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 criteria

Qualifiers

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)

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed