Synovial Sarcoma Registry and Biospecimen Repository

This study collects demographic, clinical, pathologic, molecular, imaging, treatment, and outcome data from patients with synovial sarcoma.

* Males or females of any age * Reported diagnosis of synovial sarcoma * Informed consent from subject (aged >= 18 years) or parent/guardian

* Individuals with sarcomas that do not fit the definition of those considered for this registry * Individuals who are unwilling to participate * Individuals who are unwilling or unable to provide written consent

Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05910307.

Children's Hospital of Philadelphia

Status: Active

Contact: Theodore Willis Laetsch

Phone: 267-425-0126

PRIMARY OBJECTIVES:

I. To collect demographic, clinical, pathologic, molecular, imaging, treatment, and outcome data from patients with synovial sarcoma.

II. To collect biospecimens, including tumor tissue and its excipients (DNA, RNA, protein), blood, saliva, and/or buccal swabs for future research.

OUTLINE: This is an observational study.

Patients undergo blood sample collection, complete surveys and have their medical records reviewed on study.

Trial PhaseNo phase specified

Trial TypeNot provided by clinicaltrials.gov

Lead OrganizationChildren's Hospital of Philadelphia

Principal InvestigatorTheodore Willis Laetsch

Description