LEGACY (Late Effects of GD2 Antibody and Chemotherapy in Youths): Feasibility of Screening for Early Late Effects of Contemporary Therapy in High-Risk Neuroblastoma Survivors

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The study participant is being asked to be in a research study called LEGACY, because you were treated for high-risk neuroblastoma (HR-NBL). Primary Objective To determine the feasibility of conducting comprehensive evaluations, leveraging the established SJLIFE (St. Jude Lifetime Cohort Study) study infrastructure, in survivors of HR-NBL (high-risk neuroblastoma) who are greater than 2 years from completion of contemporary therapy and were previously treated at SJCRH (St. Jude Children's Research Hospital). Exploratory Objectives * To describe the health outcomes of survivors of HR-NBL previously treated at SJCRH with contemporary era therapy who are greater than 2 years from completion of therapy. * To describe the relationship between patient outcomes and social determinants of health (SDOH) in survivors of HR-NBL previously treated at SJCRH with contemporary era therapy who are greater than 2 years from completion of therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 5
Healthy Volunteers: f
View:

• Participants were diagnosed with neuroblastoma at \< 18 years of age and categorized as high-risk at that time, according to INSS26 or INRGSS27 criteria.

• Participants were treated for HR-NBL at SJCRH on NB2012 or as per NB2012.

• Participants are ≥ 2 years from completion of therapy. Participants are 5 years of age or older.

• Participant or legal guardian is able and willing to give informed consent.

• Participants may choose to participate in all or a fraction of the proposed assessments; refusal to participate in some aspects of the study will not preclude their inclusion.

• Participants must also complete enrollment on SJLIFE.

Locations
United States
Tennessee
St. Jude Children's Research Hospital
RECRUITING
Memphis
Contact Information
Primary
Sara Federico, MD
referralinfo@stjude.org
866-278-5833
Time Frame
Start Date: 2024-10-21
Estimated Completion Date: 2028-12
Participants
Target number of participants: 45
Sponsors
Leads: St. Jude Children's Research Hospital

This content was sourced from clinicaltrials.gov