Constitution of a Centralized Biological Resources Collection and Associated With a Clinical Database for Childhood Liver Tumors Diagnosed in France (Retrospective Collection From 1990 and Prospective)

Gustave Roussy, Cancer Campus, Grand Paris1 site in 1 country600 target enrollmentSeptember 10, 2015

ConditionsLiver Tumor

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Liver Tumor
Sponsor: Gustave Roussy, Cancer Campus, Grand Paris
Enrollment: 600
Locations: 1
Primary Endpoint: Establish a national bank of rare biological material
Status: Recruiting
Last Updated: 6 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

Centralized biological collection of multicentric origin, retrospective and prospective of biological samples (tissues and fluids) taken within the framework of the diagnostic and therapeutic management of children and adolescents with liver tumor, and supported in the centers of French Society for Childhood Cancers (SFCE) with associated clinical database.

Registry

clinicaltrials.gov

Start Date

September 10, 2015

End Date

September 2025

Last Updated

6 years ago

Study Type

Observational

Sex

All

Investigators

Sponsor

Gustave Roussy, Cancer Campus, Grand Paris

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•For inclusion in the clinical database:
•Children and adolescents (≤18 years at diagnosis) suffering from a primary liver tumor diagnosed after 01/01/1990 and treated in France
•Informed consent to the computerization of data signed by the patient or by parents or legal representatives if he is a minor.
•For inclusion in the biological collection (CRB Paris Sud):
•Additional criteria:
•Availability of biological samples (tumor tissue, healthy tissue, plasma and / or serum).
•Informed consent to the use of biological remains signed by the patient or by parents or legal representatives if he is a minor.
•For the inclusion of deceased patients:
•Obtaining consent or failing this, seeking non-opposition to the computerization of data (for inclusion in the database) and the use of biological remains (for inclusion in the biological collection) of the patient or both parents or the legal guardian if he is a minor.