首页> 美国卫生研究院文献>Journal of Clinical Medicine >Immune Checkpoint Inhibitors versus VEGF Targeted Therapy as Second Line Regimen in Advanced Hepatocellular Carcinoma (HCC): A Retrospective Study
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Immune Checkpoint Inhibitors versus VEGF Targeted Therapy as Second Line Regimen in Advanced Hepatocellular Carcinoma (HCC): A Retrospective Study

机译:免疫检查点抑制剂与VEGF靶向治疗作为晚期肝细胞癌(HCC)的第二线方案:回顾性研究

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摘要

Several targeted agents including multi-tyrosine kinase inhibitors (mTKIs) and immunotherapy (IO) agents have been approved for use beyond the frontline setting in patients with advanced hepatocellular carcinoma (HCC). Due to lack of prospective head-to-head comparative trials, there is no standardized way for alternating those agents beyond frontline. Therefore, we performed a retrospective review of the Kansas University (KU) cancer registry to determine whether IO may be superior to non-IO therapy. Patients with advanced HCC were divided into two groups based on the second-line systemic regimen received (IO vs. non-IO). Progression-free survival (PFS) and overall survival (OS) were calculated under the Kaplan–Meier and Cox proportional hazards models. No statistically significant differences in PFS and OS were found, although a non-significant delayed separation in the survival curve favoring IO was identified (median PFS 3.9 months vs. 3 months; median OS 10 months vs. 10 months respectively for IO vs. non-IO). This retrospective analysis is one of the earliest and largest studies comparing second-line IO and non-IO therapies thus far reported. Future studies should aim to define specific biomarkers for response prediction and treatment optimization based on individual patient and tumor characteristics. Furthermore, combinatorial therapeutic strategies is an evolving approach showing early promising signal.
机译:已经批准了几种靶向剂,包括多酪氨酸激酶抑制剂(MTKIS)和免疫疗法(IO)试剂,用于超出肝细胞癌(HCC)患者的前线设置。由于缺乏前瞻性的头脑比较试验,没有标准化的方式是将这些代理商交替超出前线。因此,我们对堪萨斯大学(KU)癌症登记处进行了回顾性审查,以确定IO是否可能优于非IO治疗。高级HCC患者基于收到的二线系统方案(IO与非IO)分为两组。在Kaplan-Meier和Cox比例危险模型下计算了无进展生存期(PFS)和整体生存(OS)。发现了PFS和OS中没有统计学意义的差异,尽管鉴定了生存曲线中的非显着延迟分离(中位PFS 3.9个月与3个月; IO与IO与IO的中位数OS 10个月与10个月。 -io)。该回顾性分析是比较迄今为止报告的二线IO和非IO疗法的最早和最大的研究之一。未来的研究旨在确定基于个体患者和肿瘤特征的响应预测和治疗优化的特定生物标志物。此外,组合治疗策略是一种不断发展的方法,显示出早期有前途的信号。

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