This study is a single arm study to investigate the efficacy and safety of CAR-T targeted CD19/CD20/CD22/CD30 in relapse and refractory non-Hodgkin lymphoma patients. Ten patients will recruieted, admitted in hospital for 1 month for the CAR-T treatment and follow-up for at least 2 years.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
168
For eligible patients, CAR-T cells targeted to patients' tumor cell antigen will be infused after 48 hours later of chemotherapy
the First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, China
Overall Response Rate
Rate of complete remission and patial remission
Time frame: One months after CAR-T cells were infused
Adverse toxicity
Accordingto CTCAE 4.0 criteria
Time frame: Day 0, day 4, week 1, week 3, week 4, month 2, month 24 after CAR-T cells were infused
CAR-T cell survival
the survival of CAR-T cells detected in patients' peripheral blood
Time frame: every week in first 4 weeks after CAR-T cells infusion, then every 3 months for 2 years, then every 6 months for next 2 years
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