The purpose of this study is to determine whether Nivolumab given intrathecally is effective in the treatment of Relapsed/Refractory Primary Central Nervous System Lymphoma (PCNSL)
This is a case study aiming to recruit 1 patient. This study is indicated for relapsed/refractory primary central nervous system lymphoma. Primary objective is to explore the safety.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
1
Nivolumab given intraventricularly
Jianmin Zhang
Hangzhou, Zhejiang, China
Adverse events
Adverse events Adverse events assessed according to NCI-CTCAE v5.0 criteria
Time frame: On a continuous basis up to 1 month after the first dose of study drug
Best overall response(BOR)
Record individual best overall response(BOR), including CR, PR, SD, PD
Time frame: up to 3 months after the first dose of study drug
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