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Pediatric Hepatic Tumors

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)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04274868
Acronym
HEPATOBIO
Enrollment
600
Registered
2020-02-18
Start date
2015-09-10
Completion date
2025-09-30
Last updated
2020-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Tumor

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.

Interventions

None listed

Sponsors

Gustave Roussy, Cancer Campus, Grand Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years

Inclusion criteria

1. \- 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. 2. \- 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. 3. \- 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.

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
Establish a national bank of rare biological materialUp to 10 years

Countries

France

Contacts

Primary ContactBrenda Mallon
branda.mallon@gustaveroussy.fr0142114211

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026