为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Next-Generation Immunotherapy for Hepatocellular Carcinoma: Mechanisms of Resistance and Novel Treatment Approaches.
Next-Generation Immunotherapy for Hepatocellular Carcinoma: Mechanisms of Resistance and Novel Treatment Approaches.
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肝细胞癌(HCC)是全球癌症相关死亡的主要原因之一,仅有15-20%的HCC患者适合接受潜在治愈性治疗,因此绝大多数HCC患者最终需要系统性治疗。几十年来,HCC有效系统性治疗的选择一直很有限。近年来,在atezolizumab联合bevacizumab证明其总生存期优于一线标准治疗sorafenib之后,HCC的治疗范式发生了重大转变,转向以免疫治疗为基础的方案。尽管这代表了该癌症治疗的一大飞跃,但现实是不到三分之一的患者对基于免疫检查点抑制剂的治疗获得客观缓解,因此仍存在显著的临床需求以进一步优化治疗。在这篇综述中,我们概述了不可切除HCC免疫治疗的当前格局,并深入探讨了对现有免疫治疗耐药的肿瘤内在和外在机制,重点关注具有强大转化潜力的新型治疗靶点。随后,我们聚焦于新兴的免疫治疗方法以及旨在优化HCC免疫治疗疗效的显著临床试验,这些包括新型免疫检查点抑制剂、肿瘤微环境调节剂、靶向递送系统和局部区域干预。
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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