Shao Yu-Yun, Hsu Chih-Hung, Cheng Ann-Lii
Departments of Oncology, National Taiwan University Hospital, Taiwan, ROC ; Graduate Institute of Oncology, College of Medicine, National Taiwan University, Taiwan, ROC.
Liver Cancer. 2013 Apr;2(2):93-107. doi: 10.1159/000343845.
Antiangiogenic therapy, especially treatment with sorafenib, is the primary treatment for patients with advanced hepatocellular carcinoma (HCC). However, the efficacy of such therapy is modest, with low objective response rates and limited prolongation of survival times. Several researchers have investigated predictive biomarkers to help identify patients who can benefit most from antiangiogenic therapy. The largest study on this topic to date was based on the pivotal phase III study of sorafenib (the SHARP study) and did not find any plasma markers that could predict the efficacy of sorafenib. Other studies based on single-arm phase II clinical trials found some potential predictive markers, such as early alpha-fetoprotein response, the serum insulin-like growth factor-1 level at baseline, and the volume transfer constants of dynamic contrast-enhanced magnetic resonance imaging. These findings require validation by further studies. Identifying predictive biomarkers of antiangiogenic therapy for HCC remains challenging and warrants further investigations.
抗血管生成疗法,尤其是使用索拉非尼进行治疗,是晚期肝细胞癌(HCC)患者的主要治疗方法。然而,这种疗法的疗效一般,客观缓解率低,生存时间延长有限。一些研究人员已经研究了预测生物标志物,以帮助识别能从抗血管生成疗法中获益最大的患者。迄今为止,关于这个主题的最大规模研究是基于索拉非尼的关键III期研究(SHARP研究),并未发现任何可预测索拉非尼疗效的血浆标志物。其他基于单臂II期临床试验的研究发现了一些潜在的预测标志物,如早期甲胎蛋白反应、基线时血清胰岛素样生长因子-1水平以及动态对比增强磁共振成像的容积转运常数。这些发现需要进一步研究来验证。识别HCC抗血管生成疗法的预测生物标志物仍然具有挑战性,值得进一步研究。