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What is the indication for sorafenib in hepatocellular carcinoma? A clinical challenge.

机译:索拉非尼在肝细胞癌中的适应症是什么?临床挑战。

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摘要

The incidence of hepatocellular carcinoma is rising in many countries, including the United States. Approval of sorafenib (Nexavar) as the first targeted therapy for treatment of advanced hepatocellular carcinoma (HCC) represents a milestone in the treatment of this disease. The approval was based on two large randomized phase III trials from the Western and Eastern hemispheres that showed an overall survival benefit compared with placebo in patients with well-preserved liver function. The exact indication for sorafenib is unclear, however. The U.S. Food and Drug Administration (FDA) authorized use of sorafenib for "unresectable HCC", an indication which is very broad, vague, and confusing. Less is known about the effects of sorafenib in patients with decompensated liver disease, or of sorafenib in combination with local therapy or in a transplant setting. Prospective trials are lacking in these areas. We will review current data on use of sorafenib in HCC.
机译:在包括美国在内的许多国家,肝细胞癌的发病率正在上升。索拉非尼(Nexavar)作为治疗晚期肝细胞癌(HCC)的第一个靶向治疗药物的批准,代表了该疾病治疗的一个里程碑。批准是基于西半球和东半球的两项大型随机III期试验,该试验显示,在肝功能良好的患者中,与安慰剂相比,其总体生存获益。然而,索拉非尼的确切适应症尚不清楚。美国食品药品监督管理局(FDA)批准将索拉非尼用于“不可切除的HCC”,这是一个非常广泛,模糊和令人困惑的适应症。关于索拉非尼在失代偿性肝病患者中的疗效,或者索拉非尼联合局部疗法或在移植环境中的疗效知之甚少。这些领域尚缺乏前瞻性试验。我们将审查有关在肝癌中使用索拉非尼的最新数据。

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