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Biomarkers in Tissue Samples From Patients With Ewing Sarcoma

Analysis of GGAA-Microsatellites in Ewing Sarcoma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01480518
Enrollment
166
Registered
2011-11-29
Start date
2011-12-31
Completion date
2012-01-31
Last updated
2015-05-12

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

Conditions

Sarcoma

Keywords

localized Ewing sarcoma/peripheral primitive neuroectodermal tumor

Brief summary

RATIONALE: Studying samples of tissue 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 how well patients respond to treatment. PURPOSE: This research study is studying biomarkers in tissue samples from patients with Ewing sarcoma.

Detailed description

OBJECTIVES: * To describe the spectrum of GGAA-microsatellite polymorphisms at specific loci in genomic DNA prepared from Ewing sarcoma tumor specimens. * To determine if there are differences in GGAA-microsatellite polymorphisms in genomic DNA prepared from Ewing sarcoma tumor specimens as compared to non-afflicted European and African normal genomic DNA. * To determine if GGAA-microsatellite polymorphisms at specific loci in genomic DNA prepared from Ewing's sarcoma tumor specimens correlates with disease outcome in patients treated on COG protocol AEWS0031. * To determine whether whole-genome amplification introduces alterations in GGAA-microsatellites as compared to non-amplified genomic DNA. OUTLINE: Genomic PCR is used to amplify the microsatellites in the NR0B1 and GSTM4 promoters. In addition to determining microsatellite size, each microsatellite is sequenced following cloning into the pCR4 vector (Invitrogen) using standard topoisomerase cloning protocols.

Interventions

OTHERlaboratory biomarker analysis
GENETICDNA analysis
GENETICcomparative genomic hybridization
GENETICgene expression analysis
GENETICmutation analysis
GENETICpolymerase chain reaction

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Children's Oncology Group
Lead SponsorNETWORK

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 50 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Specimens from patients with Ewing sarcoma used for protocol COG-AEWS08B1 * Obtained from patient samples taken from patients enrolled on COG-AEWS0031 * Whole genome-amplified DNA will be used PATIENT CHARACTERISTICS: * Not specified PRIOR CONCURRENT THERAPY: * Not specified

Design outcomes

Primary

MeasureTime frame
Event-free survival

Outcome results

None listed

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