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Antiangiogenic treatment in hepatocellular carcinoma: the balance of efficacy and safety

机译:肝细胞癌的抗血管生成治疗:疗效与安全性的平衡

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摘要

Hepatocellular carcinoma (HCC) is a severe complication of advanced liver disease with a worldwide incidence of more than 600,000 patients per year. Liver function, clinical performance status, and tumor size are considered in the Barcelona Clinic Liver Cancer (BCLC) system. While curative treatment options are available for early stages, most patients present with intermediate- or advanced-stage HCC, burdened with a poor prognosis, substantially influenced by the degree of liver-function impairment. Hypervascularization is a major characteristic of HCC, and antiangiogenic treatments are the basis of treatment in noncurative stages, including interventional and pharmacological treatments. Currently, the tyrosine-kinase inhibitor sorafenib is still the only approved drug for HCC. Further improvements in survival in patients with intermediate- and advanced-stage HCC may be anticipated by both multimodal approaches, such as combination of interventional and systemic treatments, and new systemic treatment options. Until now, the Phase III development of other tyrosine-kinase inhibitors in patients with advanced HCC has failed due to minor efficacy and/or increased toxicity compared to sorafenib. However, promising Phase II data have been reported with MET inhibitors in this hard-to-treat population. This review gives a critical overview of antiangiogenic drugs and strategies in intermediate- and advanced-stage HCC, with a special focus on safety.
机译:肝细胞癌(HCC)是晚期肝病的严重并发症,每年在全球范围内的发病率超过60万名患者。在巴塞罗那临床肝癌(BCLC)系统中考虑了肝功能,临床表现状态和肿瘤大小。尽管早期阶段可以选择治疗,但大多数患者患有中晚期肝癌,预后较差,受肝功能损害程度的影响很大。超血管化是肝癌的主要特征,抗血管生成治疗是非治愈性阶段治疗的基础,包括介入治疗和药物治疗。目前,酪氨酸激酶抑制剂索拉非尼仍然是批准用于HCC的唯一药物。多模式方法(例如介入治疗和全身治疗的结合)以及新的全身治疗选择,可以预期中晚期肝癌患者生存率会进一步提高。到目前为止,与索拉非尼相比,由于疗效差和/或毒性增加,在晚期HCC患者中其他酪氨酸激酶抑制剂的III期开发失败。然而,已经报道了在这种难以治疗的人群中使用MET抑制剂的有希望的II期数据。这篇综述对中晚期肝癌的抗血管生成药物和策略进行了重要的概述,特别是安全性。

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