Copyright
©The Author(s) 2022.
World J Hepatol. Oct 27, 2022; 14(10): 1862-1874
Published online Oct 27, 2022. doi: 10.4254/wjh.v14.i10.1862
Published online Oct 27, 2022. doi: 10.4254/wjh.v14.i10.1862
Trial | Included population | Immunotherapy regimen | Target | Control arm | Primary outcome | Sample size |
CHECKMATE-9DX (NCT03383458) | Patients at high risk of recurrence after resection or ablation | Nivolumab | PD-1 | Placebo | RFS | 530 |
KEYNOTE-937 (NCT03867084) | Patients with complete radiological response after resection or ablation | Pembrolizumab | PD-1 | Placebo | RFS, OS | 950 |
EMERALD-2 (NCT03847428) | Patients at high risk of recurrence after resection or ablation | Durvalumab plus bevacizumab anddurvalumab plus placebo | PD-L1 | Placebo plus placebo | RFS | 888 |
IMBRAVE-050 (NCT04102098) | Patients at high risk of recurrence after resection or ablation | Atezolizumab plus bevacizumab | PD-L1 | Active surveillance | RFS | 662 |
- Citation: Cassese G, Han HS, Lee B, Lee HW, Cho JY, Panaro F, Troisi RI. Immunotherapy for hepatocellular carcinoma: A promising therapeutic option for advanced disease. World J Hepatol 2022; 14(10): 1862-1874
- URL: https://www.wjgnet.com/1948-5182/full/v14/i10/1862.htm
- DOI: https://dx.doi.org/10.4254/wjh.v14.i10.1862