Department of Hepatology, University Hospitals Leuven and Department of Clinical and Experimental Medicine, KU Leuven, Belgium.
Curr Opin Oncol. 2013 Jul;25(4):409-16. doi: 10.1097/CCO.0b013e3283621074.
Hepatocellular carcinoma (HCC) is a prevalent malignancy associated with a guarded prognosis. At present, sorafenib is the only approved systemic therapy for patients with advanced disease. The effect of sorafenib on overall survival is modest and limited in time by the occurrence of drug resistance.
Together with the increasing knowledge of molecular pathways involved in HCC, targeted molecules have been developed and tested in first and second line following sorafenib. These include antiangiogenic drugs, as well as biologicals inhibiting cell proliferation and survival. Recent phase III trials investigated sunitinib, linifanib, brivanib and erlotinib, but none of them were found superior to sorafenib. New findings in mechanisms of drug resistance create opportunities in the treatment of sorafenib-refractory disease, with cMET inhibition as the most promising approach. This article reviews the pathways involved in HCC and their targets as well as potential strategies for drug development in the future.
Advanced HCC has been the subject of intensive clinical research following the success of sorafenib. Despite many failures, some agents show promising results in phase II trials. Targeting new pathways, using multidrug regimens and tailoring treatment guided by predictive markers should allow new successes.
肝细胞癌(HCC)是一种常见的恶性肿瘤,预后较差。目前,索拉非尼是晚期患者唯一批准的系统治疗药物。索拉非尼对总生存期的影响有限,且随着耐药性的发生,其疗效会受到限制。
随着对 HCC 相关分子通路认识的不断增加,在索拉非尼之后的一线和二线治疗中,已经开发并测试了靶向分子。这些靶向药物包括抗血管生成药物以及抑制细胞增殖和存活的生物制剂。最近的 III 期临床试验研究了舒尼替尼、仑伐替尼、贝伐珠单抗和厄洛替尼,但均未发现其优于索拉非尼。耐药机制方面的新发现为索拉非尼耐药疾病的治疗创造了机会,其中 c-MET 抑制是最有前途的方法。本文综述了 HCC 相关通路及其靶点,以及未来药物开发的潜在策略。
索拉非尼成功后,晚期 HCC 一直是临床研究的热点。尽管许多药物试验失败,但一些药物在 II 期临床试验中显示出了有前景的结果。针对新的通路,使用多药物联合治疗,并根据预测标志物进行个体化治疗,应该可以取得新的成功。