Akabane Miho, Chatzipanagiotou Odysseas P, Imaoka Yuki, Schenk Austin, Pawlik Timothy M
Department of Surgery, The Ohio State University Wexner Medical Center and James Comprehensive Cancer Center, Columbus, OH, USA.
Division of Abdominal Transplant, Department of Surgery, Stanford University, Stanford, CA, USA.
Immunotargets Ther. 2025 Jun 25;14:631-654. doi: 10.2147/ITT.S528709. eCollection 2025.
Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related mortality globally, with high rates of recurrence even after curative-intent treatments such as hepatectomy and liver transplantation (LT). In recent years, immune checkpoint inhibitors (ICIs) have transformed the therapeutic landscape for HCC, demonstrating significant efficacy among advanced-stage tumors through combination regimens, such as anti-programmed cell death ligand-1 (PD-L1)/PD-1 inhibitors with anti-vascular endothelial growth factor agents. Recent advances have highlighted the potential of ICIs as adjuvant therapy to improve recurrence-free survival among high-risk patients post-resection. However, challenges such as low immunogenicity, the immunosuppressive tumor microenvironment, and immune resistance remain substantial barriers to the broader success of ICIs. In the context of LT, the use of ICIs is further complicated by the concurrent need for immunosuppressive agents, which can exacerbate the risk of recurrence. Emerging strategies focusing on the optimization of the timing of ICI therapy and the utilization of novel biomarkers are being explored to mitigate graft rejection while maintaining antitumor efficacy. Additionally, immune-cell-based therapies based on chimeric antigen receptor-T and natural killer (NK) cells, adoptive cell transfer, and liver-resident NK cell approaches are also being investigated for their potential to reduce recurrence and improve survival outcomes. This review focuses on the current landscape of adjuvant immunotherapy and immune-cell therapy in the postoperative management of HCC, highlighting ongoing clinical trials, therapeutic potential, and associated risks. With continued advancements in immunotherapeutic strategies and personalized approaches, these therapies hold the promise of transforming outcomes for patients undergoing curative resection or LT.
肝细胞癌(HCC)仍然是全球癌症相关死亡的主要原因,即使在进行了肝切除术和肝移植(LT)等根治性治疗后,复发率依然很高。近年来,免疫检查点抑制剂(ICI)改变了HCC的治疗格局,通过联合治疗方案,如抗程序性细胞死亡配体-1(PD-L1)/PD-1抑制剂与抗血管内皮生长因子药物的联合,在晚期肿瘤中显示出显著疗效。最近的进展凸显了ICI作为辅助治疗改善高危患者术后无复发生存率的潜力。然而,低免疫原性、免疫抑制性肿瘤微环境和免疫抵抗等挑战仍然是ICI更广泛成功的重大障碍。在LT的背景下,ICI的使用因同时需要免疫抑制剂而更加复杂,这可能会增加复发风险。目前正在探索侧重于优化ICI治疗时机和利用新型生物标志物的新兴策略,以减轻移植排斥反应,同时保持抗肿瘤疗效。此外,基于嵌合抗原受体T细胞和自然杀伤(NK)细胞的免疫细胞疗法、过继性细胞转移以及肝驻留NK细胞方法也在研究其降低复发和改善生存结果的潜力。本综述重点关注HCC术后管理中辅助免疫治疗和免疫细胞治疗的现状,突出正在进行的临床试验、治疗潜力和相关风险。随着免疫治疗策略和个性化方法的不断进步,这些疗法有望改变接受根治性切除或LT患者的治疗结果。