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Systemic therapy in advanced-stage hepatocellular carcinoma

机译:晚期肝细胞癌的全身治疗

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Hepatocellular carcinoma (HCC) is a complex disease, since both choice of treatment and prognosis depend not only on tumor-specific but also on liver-related characteristics. Therefore, a multidisciplinary approach in specialized clinics is required for the optimal management of HCC patients. Almost half of patients present with advanced-stage tumor with no curative therapeutic options. According to international guidelines, palliative systemic therapy is recommended in these patients. The multikinase inhibitor sorafenib was the first drug to show antitumor efficacy and was the only approved treatment for almost a decade, as several other agents failed to improve patient survival. In recent years, treatment practices have changed with lenvatinib as another first-line treatment choice and regorafenib, cabozantinib, and ramucirumab as second-line therapeutic options. However, only patients with preserved liver function (Child-Pugh-Turcotte [CPT]-A) were enrolled in these studies and are consequently suitable for these drugs. After promising phase-1 and phase-2 studies, subsequent phase-3 trials evaluating the immune checkpoint inhibitors (ICIs) nivolumab and pembrolizumab have failed to demonstrate a significant improvement in patient survival. Ongoing trials are evaluating the combination of ICIs with tyrosine kinase inhibitors or vascular endothelial growth factor (VEGF) inhibitors. Recently, in a phase-3 trial, the combination therapy atezolizumab and bevacizumab led to a significantly improved overall survival compared to sorafenib in the first-line setting. Further studies are needed to determine how best to select between the growing number of therapeutic options.
机译:肝细胞癌(HCC)是一种复杂的疾病,因为两种治疗和预后的选择不仅取决于肿瘤特异性,而且取决于肝相关的特征。因此,HCC患者的最佳管理需要专门诊所的多学科方法。几乎一半的患者患有晚期肿瘤,没有治疗治疗选择。根据国际指南,在这些患者中建议使用姑息性全身治疗。多立芯酶抑制剂索拉非尼是第一种显示抗肿瘤功效的药物,并且是几乎十年的唯一批准的治疗,因为其他几种药剂未能改善患者存活。近年来,治疗实践与Lenvatinib一样改变为另一种初系治疗选择和Regorafenib,Cabozantib和Ramucirumab,作为第二线治疗选择。然而,只有肝功能保存的患者(Child-Pugh-Turcotte [CPT] -A)注册这些研究,因此适用于这些药物。在有前途的阶段-1和第2期研究中,评估免疫检查点抑制剂(ICIS)Nivolumab和Pembrolizumab的后续相3试验未能表现出患者存活的显着改善。正在进行的试验正在评估ICIS与酪氨酸激酶抑制剂或血管内皮生长因子(VEGF)抑制剂的组合。最近,在第3期试验中,与索拉酮在第一线设置中,联合治疗atezolizumab和bevacizumab的总体存活率显着提高。需要进一步研究以确定如何最好地在越来越多的治疗选择之间进行选择。

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