Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Faculty of Medicine and Hepatitis Research Center, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Kaohsiung J Med Sci. 2021 Feb;37(2):145-153. doi: 10.1002/kjm2.12303. Epub 2020 Oct 6.
Whether patients with advanced hepatocellular carcinoma (aHCC) benefit from hepatitis C virus (HCV) eradication is uncertain. We aimed to investigate whether a survival benefit was conferred by HCV eradication in aHCC patients. This retrospective cohort study enrolled 168 HCV-infected aHCC patients from April 2013 to January 2019. All patients were treated with sorafenib. Endpoints included overall survival (OS), progression free survival (PFS), and time to liver decompensation. Patients with undetectable HCV RNA exhibited reduced aspartate aminotransferase and alpha fetoprotein levels, as well as an attenuated proportion of aHCC at initial diagnosis but increased albumin and mean sorafenib daily dosing. Patients with undetectable HCV RNA exhibited significantly longer OS compared to patients with detectable or unknown HCV RNA, which was an independent factor of OS (HR: 0.56, 95% CI: 0.350-0.903, P = .017). Patients with undetectable HCV RNA also presented a trend for longer PFS (HR 0.68, 95% CI: 0.46-1.00, P = .053). The survival benefit was considered with respect to the significantly prolonged time to Child-Pugh B scores in patients with undetectable HCV RNA (HR 0.59, 95% CI: 0.38-0.92, P = .020). Patients with detectable HCV RNA at sorafenib initiation who further received direct acting antiviral therapy also had significantly longer OS (HR 0.11, 95% CI: 0.02-0.81, P = .030) and PFS (HR 0.23, 95% CI: 0.06-0.99, P = .048). In conclusion, abolishing HCV viremia preserves liver function and confers a survival benefit in advanced HCC patients on sorafenib treatment.
是否患有晚期肝细胞癌(aHCC)的患者受益于丙型肝炎病毒(HCV)的清除尚不确定。我们旨在研究 HCV 清除是否能给 aHCC 患者带来生存获益。这项回顾性队列研究纳入了 2013 年 4 月至 2019 年 1 月期间的 168 例 HCV 感染的 aHCC 患者。所有患者均接受索拉非尼治疗。终点包括总生存期(OS)、无进展生存期(PFS)和肝功能失代偿时间。HCV RNA 不可检测的患者表现出天冬氨酸转氨酶和甲胎蛋白水平降低,以及初始诊断时 aHCC 的比例降低,但白蛋白和平均索拉非尼每日剂量增加。与 HCV RNA 可检测或未知的患者相比,HCV RNA 不可检测的患者 OS 显著延长,这是 OS 的独立因素(HR:0.56,95%CI:0.350-0.903,P =.017)。HCV RNA 不可检测的患者也表现出 PFS 延长的趋势(HR 0.68,95%CI:0.46-1.00,P =.053)。与 HCV RNA 不可检测的患者相比,Child-Pugh B 评分显著延长,这表明生存获益具有重要意义(HR 0.59,95%CI:0.38-0.92,P =.020)。在索拉非尼治疗开始时 HCV RNA 可检测但进一步接受直接作用抗病毒治疗的患者,OS(HR 0.11,95%CI:0.02-0.81,P =.030)和 PFS(HR 0.23,95%CI:0.06-0.99,P =.048)也显著延长。总之,在接受索拉非尼治疗的晚期 HCC 患者中,清除 HCV 病毒血症可保护肝功能并带来生存获益。