Department of Oncology, National Taiwan University Hospital, National Taiwan University, Taipei, Taiwan; Graduate Institute of Oncology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Department of Oncology, National Taiwan University Hospital, National Taiwan University, Taipei, Taiwan; Department of Medical Research, National Taiwan University Hospital, National Taiwan University, Taipei, Taiwan.
J Hepatocell Carcinoma. 2014 Jun 12;1:85-99. doi: 10.2147/JHC.S45040. eCollection 2014.
The approval of sorafenib, a multikinase inhibitor targeting primarily Raf kinase and the vascular endothelial growth factor receptor, in 2007 for treating advanced hepatocellular carcinoma (HCC) has generated considerable enthusiasm in drug development for this difficult-to-treat disease. However, because several randomized Phase III studies testing new multikinase inhibitors failed, sorafenib remains the standard of first-line systemic therapy for patients with advanced HCC. Field practice studies worldwide have suggested that in daily practice, physicians are adopting either a preemptive dose modification or a ramp-up strategy to improve the compliance of their patients. In addition, accumulating data have suggested that patients with Child-Pugh class B liver function can tolerate sorafenib as well as patients with Child-Pugh class A liver function, although the actual benefit of sorafenib in patients with Child-Pugh class B liver function has yet to be confirmed. Whether sorafenib can be used as an adjunctive therapy to improve the outcomes of intermediate-stage HCC patients treated with transcatheter arterial chemoembolization or early-stage HCC patients after curative therapies is being investigated in several ongoing randomized Phase III studies. An increasing number of studies have reported that sorafenib exerts "off-target" effects, including the modulation of signaling pathways other than Raf/MEK/ERK pathway, nonapoptotic cell death mechanisms, and even immune modulation. Finally, although sorafenib in combination with chemotherapy or other targeted therapies has the potential to improve therapeutic efficacy in treating HCC, it also increases toxicity. Additional clinical studies are warranted to determine useful sorafenib-based combinations for the treatment of advanced HCC.
索拉非尼是一种多激酶抑制剂,主要针对 Raf 激酶和血管内皮生长因子受体,于 2007 年被批准用于治疗晚期肝细胞癌(HCC),这在该难治性疾病的药物开发中引起了相当大的热情。然而,由于几项测试新多激酶抑制剂的随机 III 期研究失败,索拉非尼仍然是晚期 HCC 患者一线系统治疗的标准。全球的现场实践研究表明,在日常实践中,医生正在采用抢先剂量调整或爬坡策略来提高患者的依从性。此外,越来越多的数据表明,肝功能为 Child-Pugh 分级 B 的患者可以耐受索拉非尼,就像肝功能为 Child-Pugh 分级 A 的患者一样,尽管肝功能为 Child-Pugh 分级 B 的患者的确切受益仍有待确认。几项正在进行的随机 III 期研究正在调查索拉非尼是否可作为辅助治疗,以改善接受经导管动脉化疗栓塞治疗的中期 HCC 患者或根治性治疗后的早期 HCC 患者的结局。越来越多的研究报告称,索拉非尼具有“非靶点”作用,包括调节 Raf/MEK/ERK 通路以外的信号通路、非凋亡细胞死亡机制,甚至免疫调节。最后,尽管索拉非尼联合化疗或其他靶向治疗有可能提高治疗 HCC 的疗效,但也会增加毒性。需要进行更多的临床研究来确定索拉非尼在治疗晚期 HCC 方面的有效联合治疗方案。