Low Grade Glioma D33 D43
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Age < 21 years. - Histologically verified LGG Exceptions (i.e. MRI based diagnosis) can be accepted only where a biopsy would pose an unacceptable risk to damage of eloquent brain structures. - Primary diagnosis or at relapse/progression - At primary diagnosis: - Histologically verified low-grade glioma / glioneuronal tumour WHO grade I or II. - Fresh frozen and paraffin tumour material together with blood available for molecular diagnostics. -At relapse/progression: -Fresh frozen and paraffin tumour material together with blood available for molecular diagnostics from primary diagnosis and/or current episode (preferably) of relapse/progression. - No exceptions for the submission of fresh frozen and paraffin tumour material with blood - In case that the date of diagnosis is earlier than the start of LOGGIC Core in a country, submission of fresh frozen and paraffin tumour material together with blood is mandatory with no exceptions (in other words, one can include “retrospective cases” only if material is available). - Before patient registration, written informed consent, including data and tumour material transfer, must be given according to ICH/GCP, and national/local regulations. - Residency in one of the participating countries of LOGGIC Core.
Exclusion criteria
Exclusion criteria: No LGG
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Establishment of a molecular and clinical data base for pediatric low grade glioma | — |
Secondary
| Measure | Time frame |
|---|---|
| To collect molecular tumour characteristics of LGG patients for exploratory analysis of biomarker and clinical outcome. | — |
Countries
Australia, Austria, Belgium, Czechia, Denmark, Finland, Germany, Greece, Hungary, Ireland, Italy, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom
Contacts
Hopp Kindertumorzentrum Heidelberg