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©The Author(s) 2025.
World J Hepatol. Sep 27, 2025; 17(9): 107631
Published online Sep 27, 2025. doi: 10.4254/wjh.v17.i9.107631
Published online Sep 27, 2025. doi: 10.4254/wjh.v17.i9.107631
Table 1 Adjuvant therapy with molecular targeting and Immunotherapy after hepatocellular carcinoma surgery
Ref. | Drug | Type of trial | Primary end point | Result |
Molecular targeted therapy | ||||
Bruix et al[58], 2015 | Sorafenib | A phase 3, randomised, double-blind, placebo-controlled trial | RF | mRFS: 33.3 m |
Zhang et al[59], 2014 | Sorafenib | Single-center retrospective analysis | RFS and OS | RFS: 11.7 m |
OS: 32.4 m | ||||
Bai et al[60], 2022 | Lenvatinib | A retrospective analysis | Recurrence and survival rates | 1-year, 2-year recurrence rate: 15.9%, 43.2% |
1-year, 2-year survival rate: 85.8%, 71.2% | ||||
Sun et al[6], 2020 | Apatinib | Single-center, open-label, phase II trial | RFS and OS | mRFS: 7.6 m |
1-year RFS and OS: 36.1%, 93.3% | ||||
Zhou et al[62], 2022 | Lenvatinib | A multi-center, single-arm, prospective clinical trial | RFS | mRFS: 16.5 m |
Immunotherapy | ||||
Kudo et al[65], 2022 | Nivolumab | Multi-center, single-arm clinical trial | 1-year RFS | 1-year RFS: 78.6% |
Zhang et al[66], 2023 | Anti-PD-1 antibodies include camrelizumab, toripalimab, sintilimab, and pembrolizumab | Retrospective study | OS and RFS | The 1-year, 2-year, 3-year, and 4-year OS rates: 93.1%, 86.8%, 78.2%, and 51.1% |
The 1-year, 2-year, 3-year, and 4-year RFS rates: 81.7%, 77.0%, 52.3%, and 23.1% | ||||
Wang et al[67], 2024 | Sintilimab | A multicenter, open-label, randomized, controlled, phase 2 trial. | RFS | mRFS: 27.7 m |
Xu et al[68], 2023 | Pembrolizumab, tislelizumab, sintilimab, camrelizumab, and toripalimab | A retrospective, multicenter, PSM analysis | RFS and OS | mRFS: 29.6 m mOS: 35.1 m |
Targeted combination immunotherapy | ||||
Qin et al[74], 2023 | Atezolizumab, bevacizumab | A randomised, open - label, multicentre, phase 3 trial | RFS | 1-year RFS: 78% |
Xia et al[75], 2022 | Camrelizumab, apatinib | A single-arm, open label, phase II clinical trial | RFS | 1-year RFS: 53.85% |
Wang et al[76], 2023 | C + A | Retrospective cohort study | RFS and OS | mPFS: C + A: 14.0 m, C + L: 18.0 m, C + S: 12.0 m |
C + L | mOS: C + A: 17.0 m, C + L: 19.0 m, C + S: 15.0 m | |||
C + S |
- Citation: Liu F, Zhang J, Li K. Postoperative adjuvant management in hepatocellular carcinoma: A review of therapeutic efficacy and prognostic outcomes. World J Hepatol 2025; 17(9): 107631
- URL: https://www.wjgnet.com/1948-5182/full/v17/i9/107631.htm
- DOI: https://dx.doi.org/10.4254/wjh.v17.i9.107631