Fig. 1From: Decitabine in combination with fludarabine and cyclophosphamide as a lymphodepletion regimen followed by CD19/CD22 bispecific targeted CAR T-cell therapy significantly improves survival in relapsed/refractory B-ALL patientsTreatment response, overall survival probability, long-term prognosis and CAR T-cells persistence. A Clinical outcomes of patients treated with CD19/CD22 CAR T-cells. Clinical outcomes, treatment response of each patient after CD19/CD22 CAR T-cell therapy and the duration of response. Patient number is shown to the left. B–C Survival analysis. OS and LFS from the day of CAR T-cells infusion are shown for patients who received FC lymphodepletion with DAC (DAC, n = 14) compared with those who received FC alone (CON, n = 12). D–E Survival analysis of 4 subgroups. The OS and LFS were prolonged by allo-HSCT in all subgroups. F The expansion and persistence of CAR T-cells. The presence of CD19/CD22 CAR T-cells in the peripheral blood as assessed by quantitative real-time polymerase chain reaction (PCR) assay. Time points after a second CAR T-cells infusion or allo-HSCT are excluded. We analyzed the kinetics of CAR T-cell counts by using LOESS (Local Polynomial Regression) curve fitting. Bold line represents the averaged data using LOESS curve fitting approximation with the standard error in greyBack to article page