The study is to evaluate the safety and efficacy of tumor infiltrating lymphocyte (TIL) therapy for patients with maligant glioblastoma multiforme. Autologous TiLs should be given by intravenous infusion after 5 days of lymphodepletion treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
The autologous TILs will be intravenous infused into patients.
The Second Hospital of HeBei Medical University
Shijiazhuang, Hebei, China
RECRUITINGNumber of adverse events related to TiLs infusion
The primary outcome measure of this clinical trial is accessed by the safety of the TILs product. The safety profile for TILs is characterized by its incidence of the adverse events.
Time frame: 1 month
Progressional free of survival (PFS)
PFS is defined as the duration of time from start of treatment to time of progression. All patients will be followed for a minimum of 2 years.
Time frame: Up to 24 months
Objective response rate (ORR)
Time frame: 24 months
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