Efficacy and Safety of Sofosbuvir-based Regimens in Hepatitis C Patients With Decompensated Cirrhosis: A Systematic Review and Meta-analysis

被引:8
作者
Zhang, Wenyan [1 ]
Zhang, Jing [1 ]
Tang, Shan [1 ]
Liu, Yali [1 ]
Du, Xiaofei [1 ]
Qiu, Lixia [1 ]
Liu, Menglu [1 ]
Yu, Haibin [1 ]
Pan, Calvin Q. [2 ]
机构
[1] Capital Med Univ, Beijing Youan Hosp, Beijing, Peoples R China
[2] NYU, NYU Langone Hlth, Dept Med, Div Gastroenterol & Hepatol,Grossman Sch Med, New York, NY USA
关键词
Direct-acting antiviral; HCV liver failure; Sustained virologic response; Ribavirin; ACTING ANTIVIRAL THERAPY; ADVANCED LIVER-DISEASE; VIRUS-INFECTION; TREATMENT-NAIVE; PLUS RIBAVIRIN; HCV INFECTION; GENOTYPE; DACLATASVIR; PREVALENCE; LEDIPASVIR;
D O I
10.14218/JCTH.2022.00006
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Decompensated cirrhotic patients with hepatitis C (HCV) are often under-represented in clinical trials. We aimed to evaluate pooled data on the efficacy and safety of sofosbuvir (SOF)-based regimens in these patients. Methods: We conducted a systemic review and meta-analysis by searching multiple databases for studies published from October 2010 to October 2020. Outcomes of interest were sustained virologic response (SVR) and safety of SOF-based regimens in decompensated HCV patients. Two reviewers independently performed the study selection and data extraction. Results: We included 33 studies that enrolled 5,302 HCV patients. The pooled SVR rate in decompensated patients with SOF-based regimens was 85.1% (95% CI: 82.8-87.3). Patients on SOF/velpatasvir +/- ribavirin achieved a significantly higher SVR (91.0%, 95% CI: 87.7-93.9) than that of SOF/ledipasvir +/- ribavirin [(86.3%, 95% CI: 84.6-87.8); p=0.004)], or on SOF/daclatasvir +/- ribavirin (82.4%, 95% CI: 78.2-86.2%; p<0.001). Adding ribavirin to SOF-based regimens (pooled SVR 84.9%, 95% CI: 81.7-87.9) did not significantly increase the SVR [(83.8% (95% CI: 76.8-89.8%; p=0.76)] in decompensated patients, which was also true in subgroup analyses for each regimen within the same treatment duration. However, adding ribavirin significantly increased the frequency of adverse events from 52.9% (95% CI: 28.0-77.1) to 89.2% (95% CI: 68.1-99.9) and frequency of severe events. The pooled incidence of hepatocellular carcinoma and case-fatality of decompensated patients were 3.1% (95% CI: 1.5-5.0) and 4.6% (95% CI: 3.1-6.3), respectively. The overall heterogeneity was high. There was no publication bias. Conclusions: The analysis found that 12 weeks of SOF/velpatasvir without ribavirin is the preferred therapy, with a significantly higher SVR compared with other SOF-based regimens in decompensated HCV patients.
引用
收藏
页码:144 / 155
页数:12
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