Division of Hematology Oncology, Department of Medicine, University of Cincinnati Medical Center, Cincinnati, OH 45267, USA.
Department of Medicine, Northside Hospital-Gwinnett, Lawrenceville, GA 30046, USA.
Curr Oncol. 2023 Nov 7;30(11):9789-9812. doi: 10.3390/curroncol30110711.
Hepatocellular carcinoma (HCC) is the second most common cause of cancer-related deaths in the world. More than half of patients with HCC present with advanced stage, and highly active systemic therapies are crucial for improving outcomes. Immune checkpoint inhibitor (ICI)-based therapies have emerged as novel therapy options for advanced HCC. Only one third of patients achieve an objective response with ICI-based therapies due to primary resistance or acquired resistance. The liver tumor microenvironment is naturally immunosuppressive, and specific mutations in cell signaling pathways allow the tumor to evade the immune response. Next, gene sequencing of the tumor tissue or circulating tumor DNA may delineate resistance mechanisms to ICI-based therapy and provide a rationale for novel combination therapies. In this review, we discuss the results of key clinical trials that have led to approval of ICI-based therapy options in advanced HCC and summarize the ongoing clinical trials. We review resistance mechanisms to ICIs and discuss how immunotherapies may be optimized based on the emerging research of tumor biomarkers and genomic alterations.
肝细胞癌(HCC)是全球癌症相关死亡的第二大主要原因。超过一半的 HCC 患者处于晚期,高度有效的全身治疗对于改善预后至关重要。免疫检查点抑制剂(ICI)为晚期 HCC 提供了新的治疗选择。由于原发性耐药或获得性耐药,只有三分之一的患者对 ICI 治疗有客观反应。肝肿瘤微环境天生具有免疫抑制性,细胞信号通路的特定突变使肿瘤能够逃避免疫反应。接下来,对肿瘤组织或循环肿瘤 DNA 进行基因测序可以阐明对 ICI 为基础的治疗的耐药机制,并为新的联合治疗提供依据。在这篇综述中,我们讨论了导致批准 ICI 为基础的治疗方案在晚期 HCC 中的关键临床试验结果,并总结了正在进行的临床试验。我们综述了对 ICI 的耐药机制,并讨论了如何根据肿瘤生物标志物和基因组改变的新兴研究来优化免疫疗法。