The study will evaluate safety and efficacy of the CD22-targeted chimeric antigen receptor modified-T cell(CAR-T) cells in the treatment of B-cell Malignancies.
Clinical success with chimeric antigen receptor (CAR)- based immunotherapy for leukemia has been accompanied by the associated finding that antigen-escape variants of the disease are responsible for relapse. Despite anti-CD19 CAR-T exhibited the ability to re-induce remissions for many patients with relapsed and refractory B cell malignancies, a part of those patients will relapse with CD19-negative malignancies. CD22 is a type I transmembrane protein expressed on most mature B lymphocyte in the B cell malignancies,and plays a significant role in signal transduction pathway. The investigators design and conduct this trial to test the safety and effectiveness of CD22-targeted CAR-T.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
a single dose of Anti-CD22-CAR-transduced T cells will be infusion after preconditioning.
Fengtai District
Beijing, Beijing Municipality, China
RECRUITINGIncidence of adverse events related to treatment as assessed by NCI CTCAE version 4.03
Time frame: 2 years
Overall Complete Remission Rate (ORR)
Time frame: 2 years
Disease response(CR, CRi)
Time frame: 2 years
CART cells persistence in vivo
Time frame: 2 years
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