Studying Genes in Samples From Younger Patients With Adrenocortical Tumor
This study is ongoing, but not recruiting participants.
Sponsor:
Children's Oncology Group
Collaborator:
Information provided by:
National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:
NCT01528956
First received: February 5, 2012
Last updated: February 11, 2012
Last verified: February 2012
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Purpose
RATIONALE: Studying samples of blood and tumor tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer.
PURPOSE: This research trial studies genes in samples from younger patients with adrenocortical tumor.
| Condition | Intervention |
|---|---|
|
Adrenocortical Carcinoma |
Genetic: DNA methylation analysis Genetic: RNA analysis Genetic: gene expression analysis Genetic: nucleic acid sequencing Genetic: polymorphism analysis |
| Study Type: | Observational |
| Official Title: | Using New Approaches for Genomics Studies in Pediatric Adrenocortical Tumors: Whole Genome Sequencing; Deep Sequencing; miRNA; methDNA and SNP 6.0 |
Resource links provided by NLM:
MedlinePlus related topics:
Cancer
Drug Information available for:
Ribonucleic acid
U.S. FDA Resources
Further study details as provided by National Cancer Institute (NCI):
Primary Outcome Measures:
- Identification of genetic factors affecting adrenocortical tumors [ Designated as safety issue: No ]
- Comprehensive catalog of altered genes in adrenocortical samples [ Designated as safety issue: No ]
| Estimated Enrollment: | 10 |
| Study Start Date: | February 2012 |
| Estimated Primary Completion Date: | March 2012 (Final data collection date for primary outcome measure) |
OBJECTIVES:
- To perform whole-genome sequencing, deep sequencing, micro RNA analysis, methylation status, copy number variation analysis, and single-nucleotide polymorphisms (SNPs) analysis in pediatric adrenocortical tumors and compare those results to those of the same patient's normal cells.
OUTLINE: Archived tumor and blood samples are analyzed for whole-genome sequencing, deep sequencing, micro RNA , methylation status, copy variation, and single-nucleotide polymorphisms. Results are then compared with patients' normal cells.
Eligibility| Ages Eligible for Study: | up to 21 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
DISEASE CHARACTERISTICS:
- Banked tumor and blood samples obtained from patients enrolled on COG-ARAR0332 in North America and Brazil
PATIENT CHARACTERISTICS:
- Not specified
PRIOR CONCURRENT THERAPY:
- Not specified
Contacts and Locations
More Information
Additional Information:
No publications provided
| Responsible Party: | Peter C. Adamson, Children's Oncology Group - Group Chair Office |
| ClinicalTrials.gov Identifier: | NCT01528956 History of Changes |
| Other Study ID Numbers: | CDR0000724572, COG-ARAR12B1 |
| Study First Received: | February 5, 2012 |
| Last Updated: | February 11, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Cancer Institute (NCI):
|
adrenocortical carcinoma |
Additional relevant MeSH terms:
|
Adrenal Cortex Neoplasms Carcinoma Adrenocortical Carcinoma Adrenal Gland Neoplasms Endocrine Gland Neoplasms Neoplasms by Site Neoplasms |
Adrenal Cortex Diseases Adrenal Gland Diseases Endocrine System Diseases Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Adenocarcinoma |
ClinicalTrials.gov processed this record on May 16, 2013