McKeage Kate, Wagstaff Antona J
Wolters Kluwer Health, Adis, Auckland, New Zealand.
Drugs. 2007;67(3):475-83; discussion 484-5. doi: 10.2165/00003495-200767030-00009.
black triangle Sorafenib is an oral multikinase inhibitor that targets the mitogen-activated protein kinase signalling pathway and receptor tyrosine kinases involved in tumour proliferation and angiogenesis.black triangle In the large, phase III, randomised, double-blind, multicentre Treatment Approaches in Renal Cancer Global Evaluation Trial (TARGET) of patients with advanced clear-cell renal cell cancer in whom previous systemic therapy had failed, median progression-free survival was doubled in patients receiving sorafenib compared with those receiving placebo (5.9 vs 2.8mo).black triangle Significantly more patients receiving sorafenib than those receiving placebo in the phase III trial experienced complete or partial responses or stable disease.black triangle Age, risk-assessment score, prior treatment, metastasis in lung or liver, or time from diagnosis did not affect the improved progression-free survival in sorafenib recipients.black triangle In a randomised, phase II discontinuation trial of patients with advanced renal cancer, in which only those showing stable disease with sorafenib were randomised to further sorafenib or placebo, more patients receiving sorafenib were free of progressive disease 12 weeks after randomisation than were those receiving placebo, and median progression-free survival was longer in sorafenib recipients.black triangle In clinical trials, most drug-related adverse events were mild to moderate in severity. Grade 3/4 hand-foot skin reaction and hypertension occurred more often with sorafenib than with placebo.
黑三角 索拉非尼是一种口服多激酶抑制剂,可靶向参与肿瘤增殖和血管生成的丝裂原活化蛋白激酶信号通路和受体酪氨酸激酶。黑三角 在大型III期随机双盲多中心肾癌全球评估试验(TARGET)中,对于先前全身治疗失败的晚期透明细胞肾细胞癌患者,与接受安慰剂的患者相比,接受索拉非尼的患者中位无进展生存期延长了一倍(5.9个月对2.8个月)。黑三角 在III期试验中,接受索拉非尼的患者出现完全或部分缓解或疾病稳定的比例明显高于接受安慰剂的患者。黑三角 年龄、风险评估评分、先前治疗、肺或肝转移或诊断时间均不影响索拉非尼治疗患者无进展生存期的改善。黑三角 在一项针对晚期肾癌患者的随机II期停药试验中,仅将索拉非尼治疗后病情稳定的患者随机分为继续接受索拉非尼或安慰剂治疗,随机分组12周后,接受索拉非尼治疗的无进展疾病患者多于接受安慰剂治疗的患者,且索拉非尼治疗患者的中位无进展生存期更长。黑三角 在临床试验中,大多数与药物相关的不良事件严重程度为轻度至中度。与安慰剂相比,索拉非尼治疗患者3/4级手足皮肤反应和高血压的发生率更高。