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Genetics of Embryonal and Alveolar Rhabdomyosarcoma Study (GEARS)
This research trial studies genetic mutations in saliva or buccal mucosa samples from patients with embryonal or alveolar rhabdomyosarcoma. Identifying gene mutations may help doctors learn about the prognosis of patients with embryonal or alveolar rhabdomyosarcoma.
PRIMARY OBJECTIVES: I. To identify novel recurrent de novo germline mutations among rhabdomyosarcoma (RMS) case-parent trios. II. To identify the frequency of de novo germline mutations in cancer predisposition genes among RMS case-parent trios. SECONDARY OBJECTIVES: I. To conduct ?deep phenotyping? of children diagnosed with RMS utilizing questionnaire data and information from medical records. OUTLINE: Patients and their parents undergo collection of saliva or buccal mucosa samples for genetic mutational analysis. Germline deoxyribonucleic acid (DNA) from saliva or buccal mucosa is evaluated via whole exome sequencing.
Age
0 - 50 years
Sex
ALL
Healthy Volunteers
No
Childrens Oncology Group
Philadelphia, Pennsylvania, United States
Start Date
October 23, 2017
Primary Completion Date
December 31, 2022
Completion Date
December 31, 2026
Last Updated
February 6, 2026
900
ESTIMATED participants
Biospecimen Collection
PROCEDURE
Laboratory Biomarker Analysis
OTHER
Questionnaire Administration
OTHER
Lead Sponsor
Children's Oncology Group
Collaborators
NCT06669013
NCT04994132
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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