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:Immunotherapy for hepatocellular carcinoma.
Immunotherapy for hepatocellular carcinoma.
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肝细胞癌(HCC)是全球主要的健康挑战,预计到2025年每年将有超过100万患者受到影响。与其他癌症不同,HCC的发病率和死亡率持续上升,目前是全球癌症相关死亡的第三大原因。免疫检查点抑制剂(ICIs)已改变了晚期HCC的治疗格局,试验表明在一线治疗中,其总生存期获益优于索拉非尼。atezolizumab(抗PD-L1)联合bevacizumab(抗VEGF),或durvalumab(抗PD-L1)联合tremelimumab(抗CTLA-4)的联合治疗现已被公认为晚期HCC的标准治疗。近期,两项针对早期和中期疾病的ICI联合治疗III期研究分别成功达到了改善无复发生存期和无进展生存期的主要终点。尽管取得了这些进展,但与其他肿瘤类型不同,HCC中仍缺乏经过验证的ICI应答预测生物标志物。正在进行的研究致力于进一步表征肿瘤微环境,以筛选最可能从ICI中获益的患者并确定新的治疗靶点。本文中,我们综述了目前对HCC发生所处免疫微环境的认识,以及HCC中基于ICI的治疗策略的证据。
此外,我们描述了HCC中生物标志物开发的现状,以及已从临床前阶段进入早期临床试验的新型免疫治疗方法。
Hepatocellular carcinoma (HCC) is a major global healthcare challenge, with >1 million patients predicted to be affected annually by 2025. In contrast to other cancers, both incidence and mortality rates continue to rise, and HCC is now the third leading cause of cancer-related death worldwide. Immune checkpoint inhibitors (ICIs) have transformed the treatment landscape for advanced HCC, with trials demonstrating a superior overall survival benefit compared to sorafenib in the first-line setting. Combination therapy with either atezolizumab (anti-PD-L1) and bevacizumab (anti-VEGF) or durvalumab (anti-PD-L1) and tremelimumab (anti-CTLA-4) is now recognised as standard of care for advanced HCC.
More recently, two phase III studies of ICI-based combination therapy in the early and intermediate disease settings have successfully met their primary end points of improved recurrence- and progression-free survival, respectively.
Despite these advances, and in contrast to other tumour types, there remain no validated predictive biomarkers of response to ICIs in HCC. Ongoing research efforts are focused on further characterising the tumour microenvironment in order to select patients most likely to benefit from ICI and identify novel therapeutic targets.
Herein, we review the current understanding of the immune landscape in which HCC develops and the evidence for ICI-based therapeutic strategies in HCC.
Additionally, we describe the state of biomarker development and novel immunotherapy approaches in HCC which have progressed beyond the pre-clinical stage and into early-phase trials.
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