Shao Yu-Yun, Hsu Chih-Hung, Cheng Ann-Lii
Yu-Yun Shao, Chih-Hung Hsu, Ann-Lii Cheng, Graduate Institute of Oncology, National Taiwan University College of Medicine, Taipei 10051, Taiwan.
World J Gastroenterol. 2015 Sep 28;21(36):10336-47. doi: 10.3748/wjg.v21.i36.10336.
Sorafenib is the current standard treatment for advanced hepatocellular carcinoma (HCC), but its efficacy is modest with low response rates and short response duration. Predictive biomarkers for sorafenib efficacy are necessary. However, efforts to determine biomarkers for sorafenib have led only to potential candidates rather than clinically useful predictors. Studies based on patient cohorts identified the potential of blood levels of angiopoietin-2, hepatocyte growth factor, insulin-like growth factor-1, and transforming growth factor-β1 for predicting sorafenib efficacy. Alpha-fetoprotein response, dynamic contrast-enhanced magnetic resonance imaging, and treatment-related side effects may serve as early surrogate markers. Novel approaches based on super-responders or experimental mouse models may provide new directions in biomarker research. These studies identified tumor amplification of FGF3/FGF4 or VEGFA and tumor expression of phospho-Mapk14 and phospho-Atf2 as possible predictive markers that await validation. A group effort that considers various prognostic factors and proper collection of tumor tissues before treatment is imperative for the success of future biomarker research in advanced HCC.
索拉非尼是目前晚期肝细胞癌(HCC)的标准治疗药物,但其疗效有限,缓解率低且缓解持续时间短。因此,需要索拉非尼疗效的预测生物标志物。然而,确定索拉非尼生物标志物的努力仅产生了一些潜在候选物,而非临床上有用的预测指标。基于患者队列的研究确定了血管生成素-2、肝细胞生长因子、胰岛素样生长因子-1和转化生长因子-β1的血药浓度在预测索拉非尼疗效方面的潜力。甲胎蛋白反应、动态对比增强磁共振成像和治疗相关副作用可作为早期替代标志物。基于超级反应者或实验小鼠模型的新方法可能为生物标志物研究提供新方向。这些研究确定FGF3/FGF4或VEGFA的肿瘤扩增以及磷酸化Mapk14和磷酸化Atf2的肿瘤表达可能是有待验证的预测标志物。为了晚期HCC未来生物标志物研究的成功,必须开展一项综合考虑各种预后因素并在治疗前妥善收集肿瘤组织的团队工作。