Next-Generation Immunotherapy for Hepatocellular Carcinoma: Mechanisms of Resistance and Novel Treatment Approaches

被引:4
作者
Eghbali, Shabnam [1 ]
Heumann, Thatcher Ross [2 ,3 ]
机构
[1] Vanderbilt Univ, Dept Med, Div Internal Med, Med Ctr, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Dept Med, Div Hematol & Oncol, Nashville, TN 37232 USA
[3] Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
关键词
immunotherapy; hepatocellular carcinoma; angiogenesis; glypican-3; Wnt/beta-catenin; bispecific antibodies; CAR-T cell therapy; locoregional therapy; neoadjuvant; cancer vaccine; PHASE-II; OPEN-LABEL; HIGH-RISK; MULTICENTER; LENVATINIB; SORAFENIB; INHIBITOR; GROWTH; CELLS; TRIAL;
D O I
10.3390/cancers17020236
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality worldwide, and, with only 15-20% of HCC patients being suitable for potentially curative treatments, the vast majority of patients with HCC ultimately require systemic therapy. For decades, the choice of effective systemic therapy for HCC remained sparse. In recent years, after the combination of atezolizumab and bevacizumab demonstrated superior overall survival over the first-line standard, sorafenib, there has been a major therapeutic paradigm shift to immunotherapy-based regimens for HCC. While representing a great leap forward for the treatment of this cancer, the reality is that less than one-third of patients achieve an objective response to immune checkpoint inhibitor-based therapy, so there remains a significant clinical need for further therapeutic optimization. In this review, we provide an overview of the current landscape of immunotherapy for unresectable HCC and delve into the tumor intrinsic and extrinsic mechanisms of resistance to established immunotherapies with a focus on novel therapeutic targets with strong translational potential. Following this, we spotlight emerging immunotherapy approaches and notable clinical trials aiming to optimize immunotherapy efficacy in HCC that include novel immune checkpoint inhibitors, tumor microenvironment modulators, targeted delivery systems, and locoregional interventions.
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页数:28
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