Keating Gillian M
Springer, Private Bag 65901, Mairangi Bay 0754, Auckland, New Zealand.
Target Oncol. 2017 Apr;12(2):243-253. doi: 10.1007/s11523-017-0484-7.
Sorafenib (Nexavar) is currently the only systemic agent approved for use in hepatocellular carcinoma (HCC). Its approval was based on the results of the pivotal SHARP and Sorafenib Asia-Pacific (AP) trials in Child-Pugh (CP) class A patients with advanced HCC, which showed significantly longer median overall survival (OS) and time to radiological progression (TTP) with sorafenib 400 mg twice daily than with placebo, with no significant between-group difference in the median time to symptomatic progression (TTSP). Subsequent results from real-world studies such as GIDEON also support the use of sorafenib in HCC, including in carefully selected CP class B patients, although the median OS achieved in these patients appears relatively short. Sorafenib has a well characterized tolerability and safety profile, with strategies available to prevent and manage adverse effects such as hand-foot skin reactions. In conclusion, sorafenib remains an important option for the treatment of HCC.
索拉非尼(多吉美)是目前唯一被批准用于治疗肝细胞癌(HCC)的全身性药物。其获批是基于针对Child-Pugh(CP)A级晚期HCC患者开展的关键SHARP试验和索拉非尼亚太(AP)试验的结果,试验表明,每日两次服用400mg索拉非尼的患者,其总生存期(OS)和至影像学进展时间(TTP)的中位数显著长于服用安慰剂的患者,而两组间至症状性进展时间(TTSP)的中位数无显著差异。GIDEON等真实世界研究的后续结果也支持索拉非尼在HCC治疗中的应用,包括在经过精心挑选的CP B级患者中,尽管这些患者达到的OS中位数相对较短。索拉非尼具有特征明确的耐受性和安全性,有多种策略可用于预防和处理诸如手足皮肤反应等不良反应。总之,索拉非尼仍然是治疗HCC的重要选择。