This is a single-center, single-arm, open-label, dose-escalation clinical study to evaluate the safety and anti-tumor efficacy of second-line systemic chemotherapy sequential NKG2D CAR-NK cell therapy for pancreatic cancer
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
In each chemotherapy cycle, patients received 2 intravenous infusions of CAR-NK on days 2 and 3 after each chemotherapy was discontinued.
the first affiliated hospital of Zhejiang University,school of medicine
Hangzhou, Zhejiang, China
RECRUITINGMaximum tolerated dose
Determine the optimal agent for NKG2D CAR-NK at maximum tolerated dose
Time frame: within 28 days after NKG2D CAR-NK treatment
Dose limiting toxicity
Describe the adverse events of limiting further increases in the dose of NKG2D CAR-NK
Time frame: From enrollment of the first subject to completion of follow-up of the last subject up to 2 years
Effectiveness evaluation
Objective Response Rate (ORR) According to Response Evaluation Criteria In Solid Tumors Version 1.1
Time frame: At weeks 4、8 and months 3、6、9、12、16、20 and 24 after treatment
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