Bhayani Neil H, Jiang Yixing, Hamed Osama, Kimchi Eric T, Staveley-O'Carroll Kevin F, Gusani Niraj J
Penn State Milton S. Hershey Medical Center, 500 University Drive, Hershey, PA 17033-0850, USA.
Curr Clin Pharmacol. 2015;10(4):299-304. doi: 10.2174/1574884710666151020100059.
Medical therapy for hepatocellular carcinoma (HCC) is an area of active investigation because fewer than 25% of patients are candidates for curative resection or transplantation. Single agent doxorubicin, the former standard of care, generated a 10% tumor response but resulted in substantial toxicity. The resulting recommendation of the NCCN has been to administer cytotoxic chemotherapy only under clinical protocol. More recently, newer drugs with more specific targets have forced re-consideration of palliative chemotherapy in clinical practice. Bevacizumab is a promising therapy but data is limited to Phase 2 trials without impressive results. Sorafenib is the prototype multi-kinase inhibitor, which has demonstrated some but limited survival benefit in advanced HCC. This has subsequently become the standard of care. Epidermal growth factor receptor, the target of rapamycin (mTOR) pathway, transforming growth factor-β, and cyclin-dependent kinases have been recent targets of ongoing study for potential therapeutics. Overall, current therapeutics have been so promising that adjuvant therapy after curative treatment in under investigation to reduce recurrence.
肝细胞癌(HCC)的医学治疗是一个正在积极研究的领域,因为不到25%的患者适合进行根治性切除或移植。单药阿霉素曾是之前的标准治疗方法,能产生10%的肿瘤缓解率,但会导致严重毒性。美国国立综合癌症网络(NCCN)因此建议仅在临床方案下给予细胞毒性化疗。最近,具有更特异性靶点的新药促使人们在临床实践中重新考虑姑息性化疗。贝伐单抗是一种有前景的治疗方法,但数据仅限于2期试验,结果并不理想。索拉非尼是原型多激酶抑制剂,在晚期HCC中已显示出一定但有限的生存获益。这随后成为了标准治疗方法。表皮生长因子受体、雷帕霉素靶蛋白(mTOR)通路、转化生长因子-β和细胞周期蛋白依赖性激酶是目前正在研究的潜在治疗靶点。总体而言,目前的治疗方法前景广阔,正在研究根治性治疗后的辅助治疗以降低复发率。