The purpose of this study is to evaluate the safety and efficiency of CD19-Targeted CAR-T in Treating Patients with relapsed/refractory acute leukemia.
The relapsed/refractory ALL patients will receive FC (F,Fludarabine,C,Cyclophosphamide) chemotherapy followed by infusion of allogenic or autologous CD19-Targeted CAR-T cells.No graft-versus-host disease (GVHD) prevention will be conducted before or after infusion. Dose-limiting toxicity,incidence of adverse events and disease response will be detected post-infusion.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
CD19-Targeted CAR-T cells are infused to patient received FC chemotherapy
307 Hospital of PLA
Beijing, Beijing 100071, China
RECRUITINGDose-limiting toxicity
Time frame: 28 days
Incidence of adverse events as assessed
Time frame: 3 months
Disease response (CR or CRi)
Time frame: 3 months
Engraftment of transferred CD19+ CAR T cells
Time frame: 28 days
CAR19-specific antibody level
Time frame: 6 months
Duration of response
Time frame: 1year
Progression Free Survival
Time frame: 1year
Survival
Time frame: 1year
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