直接作用抗病毒药物根除HCV患者的危险因素和临床结果:一项系统回顾和荟萃分析

Infectious diseases (London, England) Pub Date : 2025-07-01 Epub Date: 2025-05-07 DOI:10.1080/23744235.2025.2493370
Hualing Li, Jiahuan Jiao, Yuyi Gu, Yu Zeng, Yunjian Sheng
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引用次数: 0

摘要

背景:在直接作用抗病毒药物(DAAs)治疗后获得持续病毒学应答(SVR)的丙型肝炎患者中,不良临床结局的发生率可以降低,但不能完全消除。本荟萃分析旨在估计丙型肝炎患者在DAAs达到SVR后的临床结局发生率。方法:在PubMed、Cochrane Library数据库、Web of Science和Embase中进行文献检索。主要终点是daa诱导丙型肝炎病毒(HCV)消除后肝细胞癌(HCC)发生、HCC复发、失代偿性肝硬化和肝脏相关死亡率的发生率。根据年龄、性别、合并症、地区、纤维化分期、有无失代偿、随访时间、随访起始点和HCC治疗方式进行亚组分析。此外,进行meta回归以探索高异质性的来源。结果:132篇文章被纳入我们的研究。合并HCC发生率为1.50/100人年(95% CI, 1.35-1.65), HCC复发率为17.00/100人年(95% CI, 13.83-20.42),失代偿率为0.30/100人年(95% CI, 0.16-0.48),肝脏相关死亡率为0.32/100人年(95% CI, 0.14-0.56)。meta回归显示随访时间和纤维化分级是HCC发生的重要因素。年龄、随访起始点、随访时间是影响HCC复发率的重要因素。结论:daa诱导的HCV消除患者仍然存在不良结局的风险,特别是那些有肝硬化和HCC病史的患者。随着时间的推移,不良后果的暴露倾向于减少,并且随访的频率和强度可能在未来减少,这将需要新的评分模型来识别这些个体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk factors and clinical outcomes in patients with HCV eradication by direct-acting antivirals: a systematic review and meta-analysis.

Background: In hepatitis C patients with sustained virologic response (SVR) achieved after direct-acting antivirals (DAAs), the incidence of adverse clinical outcomes can be reduced but not completely eliminated. This meta-analysis aims at estimating the incidence of clinical outcomes in hepatitis C patients after achieving SVR with DAAs.

Methods: Literature search was carried out in PubMed, Cochrane Library database, Web of Science, and Embase. The primary endpoint was the incidence of hepatocellular carcinoma (HCC) occurrence, HCC recurrence, decompensated cirrhosis, and liver-related mortality, following DAA-induced elimination of hepatitis C virus (HCV). Subgroup analyses were performed according to age, gender, comorbidities, region, fibrosis stage, presence of decompensation, duration of follow-up, start point of follow-up, and HCC treatment modality. Furthermore, meta-regression was performed to explore sources of high heterogeneity.

Results: Finally, 132 articles were included in our study. The pooled HCC occurrence rate was 1.50/100 person-years (95% CI, 1.35-1.65), HCC recurrence rate was 17.00/100 person-years (95% CI, 13.83-20.42), decompensation rate was 0.30/100 person-years (95% CI, 0.16-0.48), and liver-related mortality was 0.32/100 person-years (95% CI, 0.14-0.56). Meta-regression showed that duration of follow-up and fibrosis grade were important contributors to HCC occurrence. Age, start point of follow-up, and duration of follow-up were important contributors to HCC recurrence rate.

Conclusion: Patients with DAA-induced HCV elimination remain at risk for adverse outcomes, particularly those with cirrhosis and HCC history. The exposure to adverse outcomes tended to decrease over time, and the frequency and intensity of follow-up might be reduced in the future, which will require new scoring models to identify these individuals.

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