CAR T-cell Long-Term Follow-Up, Quality of Life and Adverse Reactions
Objective: To evaluate the feasibility of conducting standardized clinical assessments of pediatric, adolescent and young adult (AYA) B-ALL survivors post CD19-CAR T-cell therapy, treated at multiple institutions, leveraging the St Jude Lifetime Cohort (SJLIFE) clinical and research infrastructure. Exploratory
Objectives: * To describe the prevalence of persistent and new/late-onset health conditions developing ≥2-years post CD19-CAR T-cell therapy in survivors of pediatric and AYA B-ALL. * To characterize neurocognitive and neurologic function in survivors ≥2-years post CD19- CAR T-cell therapy. * To characterize immune health in survivors ≥2-years post CD19-CAR T-cell therapy. * To characterize functional status in survivors ≥2-years post CD19-CAR T-cell therapy.
• ≤ 26-years old at the time of the first CAR treatment
• Receipt of a CD19-containing CAR T-cell product (investigational or commercial) for B- ALL
• Receipt of one unique CAR product (reinfusion of same product allowed)
• Sustained remission without subsequent therapy post-CAR (exception= post-CAR consolidative HCT)
• Receipt of only one prior HCT (inclusive of pre- or post-CAR)
• ≥ 2-years post last CAR T-cell infusion