TABLE 1.
Trial | Patients | Agent (target) | Phase, arm | Study design | Size | Primary endpoint | |
---|---|---|---|---|---|---|---|
ATTRACTION-5 (NCT03006705) | - | Nivolumab (PD-1) | III, two-arm | Nivolumab + S-1/CAPOX | 377 | 3-year RFS | 68.4% |
Placebo + S-1/CAPOX | 378 | 65.3% | |||||
JUPITER-15 (NCT05180734) | - | Toripalimab (PD-1) | III, two-arm | Toripalimab + SOX/XELOX | 340 | DFS | |
Placebo + SOX/XELOX | 340 | ||||||
NCT05184946 | - | Camrelizumab (PD-1) | II, two-arm | Camrelizumab + SOX | 36 | 3-year DFS | |
SOX only | 36 | ||||||
NCT05468138 | dMMR/MSI-H | Sintilimab/Nivolumab (PD-1) | II/III, three-arm | Sintilimab/Nivolumab only | 141 | 3-year DFS | |
SOX/XELOX only | |||||||
observation | |||||||
NCT05769725 | PD-L1CPS≥5/EBV+/dMMR/MSI-H | Serplulimab (PD-1) | II, two-arm | Serplulimab + DS | 35 | 1-year DFS | |
DS only | 35 | ||||||
NCT04997837 | D2/R0 resected with pN3 | multiple PD-1 inhibitors | III, two-arm | PD-1+CRT | 433 | 3-year DFS | |
Chemotherapy |
CAPOX: Capecitabine + Oxaliplatin; XELOX: Xeloda + Oxaliplatin; SOX: S-1 + Oxaliplatin; DS: Docetaxel + S-1; CRT: chemoradiotherapy; RFS: recurrence free survival; DFS: disease free survival.