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. 2024 May 9;15:1391562. doi: 10.3389/fphar.2024.1391562

TABLE 1.

Clinical trials of ICIs in adjuvant setting.

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.