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Clinical Trials/NCT00891722
NCT00891722
Unknown
Not Applicable

Translation Study for Children and Adolescents With Low Grade Glioma

Children's Cancer and Leukaemia Group1 site in 1 country900 target enrollmentAugust 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Brain and Central Nervous System Tumors
Sponsor
Children's Cancer and Leukaemia Group
Enrollment
900
Locations
1
Primary Endpoint
Identification of factors that could determine different patterns of tumor development, natural tumor behavior, and tumor sensitivity to therapies
Last Updated
12 years ago

Overview

Brief Summary

RATIONALE: Studying samples of tumor tissue and blood in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors understand why low-grade gliomas develop in young patients and predict how they will respond to treatment.

PURPOSE: This clinical trial is studying tumor tissue, blood samples, and family history in predicting tumor development and response to treatment in young patients with low-grade glioma.

Detailed Description

OBJECTIVES: * To develop a better understanding of why low-grade glioma tumors develop in children and adolescents. * To study genetic profiles that may predict response to treatment and provide clues to how these tumors developed initially using tumor and blood samples from these patients. OUTLINE: This is a multicenter study. * Retrospective data collection (for participants recruited from study SIOP-LGG1): During a follow-up appointment for study SIOP-LGG1, both biological parents\* are asked to complete a questionnaire about their family's cancer history. They may complete the questionnaire either in the clinic or in their home. Participants may complete and return the questionnaires at any time throughout the study. * Prospective data collection (for participants recruited from study SIOP-LGG-2004): Both biological parents\* are asked to complete a family history questionnaire and provide information about their family's cancer history. Participants may complete and return the questionnaires at any time throughout the study. NOTE: \*In circumstances where either or both biological parents are unable to complete the questionnaire, it may be completed by the patient diagnosed with low grade glioma (if they are over 16 years old) or adoptive parents or guardians, if they feel they have the knowledge to complete the questionnaire. Tumor tissue and blood samples collected on SIOP-LGG1 or SIOP-LGG-2004 are analyzed for genetic profiles predictive of response to treatment and for different patterns of tumor development, natural tumor behavior, and tumor sensitivity to cancer therapies. Collected family data are anonymised and linked to the biological sample collected. Samples are then stored for future molecular genetic studies.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
TBD
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Children's Cancer and Leukaemia Group

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Identification of factors that could determine different patterns of tumor development, natural tumor behavior, and tumor sensitivity to therapies

Study Sites (1)

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