This is an open-label, four-cohort, phase 2 study to determine the efficacy of CART19 in pediatric and young adult patientswith hypodiploid (Cohort A) or t(17;19) B-ALL (Cohort B), infants with very high risk KMT2A B-ALL (Cohort C), and in patients with central nervous system (CNS) relapse who did not receive cranial radiation (XRT) or bone marrow transplantation (BMT) (Cohort D).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
133
CART19 cells transduced with a lentiviral vector to express anti-CD19 scFv:41-BB:TCRζ, administered by IV injection with a planned dose of 5x106 CART19 cells/kg on day 0 with possible reinfusion/retreatment
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
RECRUITINGEvent-free survival (EFS)
1 year event-free survival (EFS), where events include no response, relapse, death due to any cause
Time frame: One year
EFS Rate 1
Modified EFS rate in CNS relapse patients, using a definition of events that includes no response, relapse, death, need for XRT or need for BMT
Time frame: One year
To further evaluate the safety of CART19 in the target patient populations
Frequency and severity of adverse events
Time frame: One year
EFS rate 2
Modified EFS rate in patients with early CNS relapsed B-ALL (CR1 \<18 months) and those with late CNS relapsed B-ALL (CR1 \>18 months) using a definition of events that includes no response, relapse, death, need for XRT or need for BMT
Time frame: One year
MRD conversion
Rate of MRD conversion to less than 0.01% (in patients with MRD) 28 days after CART19 therapy in patients with t(17;19) B-ALL, hypodiploid B-ALL, and very high risk infant B-ALL
Time frame: One year
Relapse Free survival 1
Relapse-free survival (RFS) at one year in patients with hypodiploid B-ALL, patients with t(17;19) B-ALL, and very high risk infant B-ALL regardless of their initial response to B-ALL therapy and in patients with CNS relapse who did not receive cranial XRT or BMT after CART19 and who achieved a complete remission following CART19 therapy.
Time frame: One year
Relapse Free survival 2
RFS at one year in patients with hypodiploid B-ALL who were MRD negative at end of induction and those who were MRD positive at end of induction during upfront therapy
Time frame: One year
Relapse Free survival 3
RFS at one year in patients with t(17;19) B-ALL who were MRD negative at end of induction and those who were MRD positive at end of induction during upfront therapy
Time frame: One year
Relapse Free survival 4
RFS at one year in very high risk infants with KMT2A rearrangement who were MRD negative at end of induction and those who were MRD positive at end of induction.
Time frame: One year
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