32
Participants
Start Date
October 31, 2025
Primary Completion Date
December 31, 2026
Study Completion Date
December 31, 2027
Sintilimab+Temozolomide+Surufatinib
After fully informed and signed informed consent, subjects will receive Sintilimab (200mg each fixed dose, once every 21 days) combined with Temozolomide (BSA≤1.7m2; BSA \> 1.7m2 was administered with 300mg, QD, d1-d5, and with Surufatinib (250mg, QD, continuous administration). A treatment cycle of 21 days until disease progression, death, toxicity intolerance or withdrawal of informed consent, with a maximum treatment period of 24 months.
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
OTHER