Tumor Tissue, Blood Samples, and Family History in Predicting Tumor Development and Response to Treatment in Young Patients With Low-Grade Glioma
Recruitment status was Recruiting
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
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.
| Condition | Intervention |
|---|---|
|
Brain and Central Nervous System Tumors |
Other: biologic sample preservation procedure Other: laboratory biomarker analysis Other: questionnaire administration |
| Study Type: | Observational |
| Official Title: | Translation Study for Children and Adolescents With Low Grade Glioma |
- Identification of factors that could determine different patterns of tumor development, natural tumor behavior, and tumor sensitivity to therapies [ Designated as safety issue: No ]
| Estimated Enrollment: | 900 |
| Study Start Date: | August 2008 |
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.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
DISEASE CHARACTERISTICS:
Biological parents of a child or adolescent patient diagnosed with low grade glioma (LGG)
LGG patients participating in 1 of the following clinical trials:
- On active follow up for study SIOP-LGG1 at a Children's Cancer and Leukemia Group center
- On study SIOP-LGG-2004
- Adoptive parents or guardians allowed if they feel they have the knowledge to complete the study questionnaire, provided either or both biological parents are unable to complete the questionnaire
PATIENT CHARACTERISTICS:
- Not specified
PRIOR CONCURRENT THERAPY:
- Not specified
Contacts and Locations| United Kingdom | |
| Queen's Medical Centre | Recruiting |
| Nottingham, England, United Kingdom, NG7 2UH | |
| Contact: Contact Person 44-115-924-9924 ext. 61727 | |
| Principal Investigator: | David A. Walker | Queen's Medical Centre |
More Information
Additional Information:
No publications provided
| ClinicalTrials.gov Identifier: | NCT00891722 History of Changes |
| Other Study ID Numbers: | CDR0000614912, CCLG-CNS-2007-13-TRANSCAL, EU-20879 |
| Study First Received: | April 30, 2009 |
| Last Updated: | July 1, 2009 |
| Health Authority: | Unspecified |
Keywords provided by National Cancer Institute (NCI):
|
recurrent childhood brain stem glioma untreated childhood brain stem glioma recurrent childhood cerebellar astrocytoma untreated childhood cerebellar astrocytoma childhood low-grade cerebral astrocytoma |
recurrent childhood cerebral astrocytoma childhood oligodendroglioma recurrent childhood visual pathway and hypothalamic glioma untreated childhood visual pathway and hypothalamic glioma childhood mixed glioma |
Additional relevant MeSH terms:
|
Glioma Nervous System Neoplasms Central Nervous System Neoplasms Neoplasms, Neuroepithelial Neuroectodermal Tumors Neoplasms, Germ Cell and Embryonal |
Neoplasms by Histologic Type Neoplasms Neoplasms, Glandular and Epithelial Neoplasms, Nerve Tissue Neoplasms by Site Nervous System Diseases |
ClinicalTrials.gov processed this record on June 18, 2013