80
Participants
Start Date
July 20, 2025
Primary Completion Date
July 19, 2029
Study Completion Date
July 19, 2029
Surufatinib
Administered orally at 200 mg once daily d1-d14, starting at the initiation of each radiotherapy phase, for 14 consecutive days. Six weeks after completion of concurrent chemoradiotherapy, patients meeting the eligibility criteria will receive consolidation therapy with surufatinib 200 mg orally once daily on Days 1-14 of each 21-day cycle
Tislelizumab
200 mg administered via intravenous drip one day prior to the start of each radiotherapy phase. Six weeks after completion of concurrent chemoradiotherapy, patients meeting the eligibility criteria will receive consolidation therapy with tislelizumab 200 mg administered via intravenous drip on Day 1 of each cycle (Q3W), for up to 12 months.
Concurrent Chemotherapy
Albumin-bound paclitaxel 50 mg/m² plus cisplatin 25 mg/m², administered weekly (QW).
Radiotherapy
definitive hypofractionated radiotherapy
RECRUITING
Sun yat-sen University Cancer Center, Guangzhou
Sun Yat-sen University
OTHER