Department of Epidemiology and Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China.
Key Laboratory of Infectious Diseases, School of Public Health, Nanjing Medical University, Nanjing, China.
Carcinogenesis. 2018 Dec 31;39(12):1497-1505. doi: 10.1093/carcin/bgy099.
It has been proven that hepatitis C virus (HCV) eradication after interferon-based treatment can reduce the risk of hepatocarcinogenesis. However, there were some arguments about whether the treatment of direct-acting antivirals (DAAs) boosts the development of hepatocellular carcinoma (HCC). We systematically review this crucial topic by combining all the relevant articles to calculate the pooled HCC density after DAA treatment. Studies reporting the recurrence or occurrence in chronic hepatitis C patients who received DAA regimen were selected from three retrieval library screening. Data on baseline and outcomes were extracted independently by three observers. Primary outcomes were incidence density of HCC. Pooled estimates of HCC occurrence and recurrence rate per 100 person-years (py) were undertaken by random-effects meta-analysis. Sixteen studies with 61334 patients, embracing 20 cohorts, were enrolled in this study and divided into two groups (HCC occurrence and HCC recurrence). In the pooled analysis, HCC developed at a rate of 3.5/100 py [95% confidence interval (CI): 2.4, 5.3] among patients without a history of HCC compared with 17.4/100 py (95% CI: 7.8, 39.0) among patients existed. Furthermore, HCC occurrence rate following DAA-induced sustained virological response (SVR) was 2.1/100 py (95% CI: 1.4, 3.4); however, the rate in patients without SVR was 9.1/100 py (95% CI: 5.4, 15.3). HCV cured after DAA therapy could induce a reduction of 78% in the risk of HCC occurrence compared with non-responders. There is no strong evidence for an increased risk of HCC occurrence or recurrence in patients treated by DAA. There was a significant decline in the incidence of HCC occurrence after SVR.
已证实,基于干扰素的治疗后丙型肝炎病毒 (HCV) 的清除可降低肝癌发生的风险。然而,关于直接作用抗病毒药物 (DAA) 的治疗是否会促进肝细胞癌 (HCC) 的发展存在一些争议。我们通过综合所有相关文章来计算 DAA 治疗后的 HCC 密度,从而系统地回顾了这一关键问题。从三个检索库筛选中选择了报告接受 DAA 方案治疗的慢性丙型肝炎患者复发或发生的研究。由三位观察者独立提取基线和结局数据。主要结局是 HCC 的发病率密度。通过随机效应荟萃分析对 HCC 发生率和每 100 人年 (py) 的 HCC 复发率进行汇总估计。这项研究共纳入了 16 项研究,共 61334 例患者,包含 20 个队列,并分为两组 (HCC 发生和 HCC 复发)。在汇总分析中,无 HCC 病史的患者 HCC 的发病率为 3.5/100 py [95%置信区间 (CI):2.4,5.3],而存在 HCC 的患者为 17.4/100 py (95% CI:7.8,39.0)。此外,DAA 诱导的持续病毒学应答 (SVR) 后 HCC 发生率为 2.1/100 py (95% CI:1.4,3.4);然而,无 SVR 的患者 HCC 发生率为 9.1/100 py (95% CI:5.4,15.3)。DAA 治疗后 HCV 被清除可使 HCC 发生的风险降低 78%。没有证据表明 DAA 治疗的患者 HCC 发生或复发的风险增加。SVR 后 HCC 发生的风险显著下降。