EULAT Eradicate GBC

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Paul Strauss

About this trial

Gallstones are relatively frequent in women and constitute one of the main risk factors for gallbladder cancer (GBC).

Currently, GBC diagnosis is mainly based on imaging (ultrasound or abdominal CT) associated with invasive examinations (biopsy and surgery), with no marker available to date to accurately predict risk and diagnose the disease early. The only curative treatment for GBC remains surgery with complete resection of tumors in early stages.

Given the aggressiveness of GBC and the very limited therapeutic options, as well as the possibility of preventing GBC by cholecystectomy during the 10 to 20 years required for the development of gallbladder tumors, it is imperative to develop effective and efficient prevention strategies based on a prioritization of interventions according to environmental and genetic-molecular risk factors.

The investigators aim to identify epidemiological factors linked to the development of GBC, and to identify, validate and functionally characterize genetic-molecular markers in blood, saliva, urine, bile and stool that allow risk prediction, early diagnosis and precision treatment of incidental tumors.

Eligibility criteria

Qualifiers

Cohort A. Patients with gallbladder cancer or dysplasia, both before and after the start of their anticancer treatment.

Diagnosis confirmed in accordance with standard protocols of the participating hospitals

Men and women aged 18 or over

Disqualifiers

Any medical condition that present an unreasonable risk to the participant.

Any psychiatric condition that interferes with understanding informed consent.

Trial design

Treatments tested in this trial

  • None, observational study.

Treatment groups

15,000 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Centre Paul Strauss

Lead sponsor

University Hospital Heidelberg

Collaborator

Universidad Austral de Chile

Collaborator

Universidad de La Frontera

Collaborator

Universidad Católica del Maule

Collaborator

Centre international de recherche sur le cancer (IARC, France)

Collaborator

University of Chile

Collaborator

Instituto Nacional de Enfermedades Neoplásicas (INEN, Peru)

Collaborator

Universidad Mayor de San Simón (UMSS, Bolivia)

Collaborator

Oslo University Hospital

Collaborator

Sanatorio el Carmen (Argentina)

Collaborator

Pontificia Universidad Catolica de Chile

Collaborator

University of Bristol

Collaborator

University of Oslo

Collaborator

Chilean institutions (See detailed study description below)

Collaborator

Peruvian institutions (See detailed study description below)

Collaborator

Bolivian institutions (See detailed study description below)

Collaborator

Argentinian institutions (See detailed study description below)

Collaborator