Gafton Bogdan, Porumb Vlad, Ungurianu Simona, Marinca Mihai Vasile, Cocea Corina, Croitoru Adina, Balan Gheorghe, Miron Nicolae, Eliade Ciuleanu Tudor, Miron Lucian
The University of Medicine and Pharmacy "Gr. T. Popa", Iasi, Romania.
J BUON. 2014 Oct-Dec;19(4):858-66.
Hepatocellular carcinoma has an increasing incidence and an impressive mortality. At present, the only authorized systemic treatment is the multi-kinase inhibitor sorafenib. A multitude of clinical trials are aimed at improving outcomes, both in firstY- and in second-line therapy. In this multitude of clinical trials, the purpose of our article was to familiarize physicians with the mechanisms of action of new biological therapies and to offer an algorithm for optimal trial selection for each patient, based on clinical and biological indicators. The available data were structured as follows: antiangiogenic therapy, c -MET inhibitors, combinations of chemotherapy with sorafenib, immune response modulators, cellular metabolism modulators, mTOR inhibitors, other multi-kinase inhibitors.
Treatment of advanced hepatocellular carcinoma remains a challenge for oncologists. Choosing the "right" trial may be the only chance of prolonging patient survival and improve his/her clinical status.
肝细胞癌的发病率呈上升趋势,死亡率令人震惊。目前,唯一获批的全身治疗药物是多激酶抑制剂索拉非尼。众多临床试验旨在改善一线和二线治疗的疗效。在众多此类临床试验中,我们撰写本文的目的是让医生熟悉新型生物疗法的作用机制,并根据临床和生物学指标为每位患者提供优化试验选择的算法。现有数据按以下方式分类:抗血管生成疗法、c-MET抑制剂、化疗与索拉非尼联合用药、免疫反应调节剂、细胞代谢调节剂、mTOR抑制剂、其他多激酶抑制剂。
晚期肝细胞癌的治疗对肿瘤学家来说仍然是一项挑战。选择“正确”的试验可能是延长患者生存期并改善其临床状况的唯一机会。