The goal of this clinical trial is to evaluate the safety and efficacy of oncolytic virus TS-2021 in the treatment of recurrent malignant glioma.About 30 eligible participants with recurrent malignant glioma will : * Be intratumoral injected the TS-2021 oncolytic virus to study its safety and efficacy. * Be followed for 1 year after the injection to complete imaging studies, neurological function tests, and report adverse events. Using the data obtained during the follow-up period, researchers will conduct statistical analyses and evaluate the safety and efficacy of oncolytic virus TS-2021.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
The participants meeting the criteria will undergo TS-2021 oncolytic virus (5×1011PFU/ml) intratumoral injection using stereotactic technique under MR Localization.
Beijing Tiantan Hospital
Beijing, Beijing Municipality, China
RECRUITINGIncidence and severity of adverse events.
All events with a Grade 3 or above toxicity (defined by the CTCAE v4.0) will be tabulated by event and by relationship to TS-2021.
Time frame: Up to 8 weeks
Overall survival
The overall survival for each patient receiving TS-2021 will be calculated.
Time frame: Up to 12 months
Objective response rate (ORR) determined by MRI scan review.
Interval tumor size change will be measured.
Time frame: Up to 12 months
Progression Free Survival.
Time after TS-2021 administration to clinical and radiographic disease progression
Time frame: Up to 12 months
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