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Drugs. 2015 Jun;75(9):1009-17. doi: 10.1007/s40265-015-0406-x.
Regorafenib (Stivarga(®)) is an orally administered small molecule inhibitor of multiple protein kinases, including kinases involved in oncogenesis and tumour angiogenesis. It was initially approved for use in patients with previously treated metastatic colorectal cancer. Based on the findings of the phase III GRID clinical trial, approval for regorafenib has been expanded to include the treatment of advanced gastrointestinal stromal tumours (GISTs) following the failure of imatinib and sunitinib. In the GRID trial, regorafenib significantly improved progression-free survival and was associated with a significantly higher disease control rate than placebo. No significant between-group difference was observed in overall survival (OS) in the trial; however, the high proportion of patients who crossed over from placebo to regorafenib likely impacted the OS analysis. Regorafenib has an acceptable tolerability profile, with most adverse events being manageable with dose modification and/or supportive measures. The most commonly reported drug-related adverse events among patients receiving regorafenib in the GRID trial were hand-foot skin reaction, hypertension, diarrhoea and fatigue. In conclusion, regorafenib presents a valuable new tool in the treatment of patients with advanced GISTs following the failure of imatinib and sunitinib.
瑞戈非尼(Stivarga(®))是一种口服小分子多激酶抑制剂,包括参与肿瘤发生和肿瘤血管生成的激酶。它最初被批准用于治疗先前治疗过的转移性结直肠癌患者。基于 III 期 GRID 临床试验的结果,批准瑞戈非尼用于伊马替尼和舒尼替尼治疗失败后的晚期胃肠道间质瘤(GIST)的治疗。在 GRID 试验中,瑞戈非尼显著改善了无进展生存期,并且疾病控制率明显高于安慰剂。试验中两组之间的总生存期(OS)没有观察到显著差异;然而,安慰剂组中大量患者交叉到瑞戈非尼组可能影响了 OS 分析。瑞戈非尼具有可接受的耐受性特征,大多数不良反应可以通过剂量调整和/或支持性措施来控制。在 GRID 试验中接受瑞戈非尼治疗的患者中最常报告的药物相关不良反应是手足皮肤反应、高血压、腹泻和疲劳。总之,瑞戈非尼是一种有价值的新工具,可用于治疗伊马替尼和舒尼替尼治疗失败后的晚期 GIST 患者。