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Sorafenib: in hepatocellular carcinoma.

机译:索拉非尼:在肝细胞癌中。

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摘要

Sorafenib is an orally active multikinase inhibitor with anti-tumour activity. It was recently approved in the US and the EU for the treatment of patients with hepatocellular carcinoma. Oral sorafenib 400 mg twice daily significantly improved survival in patients with advanced hepatocellular carcinoma in the randomized, double-blind, multicentre, phase III SHARP trial (n = 602); the median duration of survival was 10.7 months with sorafenib and 7.9 months with placebo. In addition, the median time to progression was significantly longer in patients receiving sorafenib than in those receiving placebo (5.5 vs 2.8 months). Combination therapy with oral sorafenib 400 mg twice daily and intravenous doxorubicin has potential in the treatment of patients with advanced hepatocellular carcinoma, according to the results of a randomized, double-blind, phase II study (n = 96). Although the addition of sorafenib to doxorubicin did not significantly delay the time to progression, the median durations of overall survival and progression-free survival were significantly longer with sorafenib plus doxorubicin than with doxorubicin alone. Monotherapy with oral sorafenib 400 mg twice daily was generally well tolerated in patients with advanced hepatocellular carcinoma, with a manageable adverse event profile.
机译:索拉非尼是一种具有抗肿瘤活性的口服活性多激酶抑制剂。最近在美国和欧盟获得批准,可用于治疗肝细胞癌患者。在随机,双盲,多中心,III期SHARP试验中,口服索拉非尼400 mg每天两次,可显着提高晚期肝细胞癌患者的生存率(n = 602);索拉非尼组的中位生存期为10.7个月,安慰剂组为7.9个月。另外,接受索拉非尼治疗的患者中位进展时间显着长于接受安慰剂的患者(5.5 vs 2.8个月)。根据一项随机,双盲,II期研究(n = 96)的结果,口服两次口服索拉非尼400 mg每天两次与静脉注射阿霉素的联合治疗在晚期肝细胞癌的治疗中具有潜力。尽管在阿霉素中添加索拉非尼并没有显着延迟进展时间,但索拉非尼加阿霉素的总生存期和无进展生存期的中位数比单独使用阿霉素的生存期显着更长。晚期肝细胞癌患者一般每天口服两次口服索拉非尼400 mg的单药治疗耐受性良好,不良事件可控。

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