Patients with relapsed or refractory lymphoma often develop resistance to chemotherapy. Chimeric antigen receptor-modified T cell (CART) therapy showed promising effect in B-cell malignancies these years. CD19 and CD22 are proteins expressed on the surface of the lymphoma cells in patients with CD19+CD22+ lymphoma. The CAR enables the T-cells to recognize and kill the tumor cell through recognition of CD19 and CD22. This is a phase 2 trial to study the safety and efficacy of dual specificity CD19 and CD22 CAR-T cell immunotherapy for CD19+CD22+ relapsed and refractory lymphoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Patient-derived dual specificity CD19 and CD22 CAR-T Cells
Shanghai Ruijin Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGOverall remission rate
Rate of complete remission and patial remission
Time frame: 4 weeks after infusion
Adverse toxicity
According to CTCAE 4.0 criteria
Time frame: Day 0, day 4, week 1, week 3, week 4, month 2, month 12 after CAR-T cells were infused
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