The risk of hepatitis C virus recurrence in hepatitis C virus-infected patients treated with direct-acting antivirals after achieving a sustained virological response: A comprehensive analysis

被引:5
|
作者
Huang, Peng [1 ,2 ,3 ]
Wang, Yan [1 ]
Yue, Ming [4 ]
Ge, Zhijun [5 ]
Xia, Xueshan [6 ]
Jeyarajan, Andre J. [2 ,3 ]
Holmes, Jacinta A. [7 ]
Yu, Rongbin [1 ]
Zhu, Chuanwu [8 ]
Yang, Sheng [9 ]
Lin, Wenyu [2 ,3 ]
Chung, Raymond T. [2 ,3 ]
机构
[1] Nanjing Med Univ, Ctr Global Hlth, Sch Publ Hlth, Dept Epidemiol, Nanjing, Peoples R China
[2] Harvard Med Sch, Liver Ctr, Massachusetts Gen Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Med Sch, Gastrointestinal Div, Massachusetts Gen Hosp, Dept Med, Boston, MA 02115 USA
[4] Nanjing Med Univ, Dept Infect Dis, Affiliated Hosp 1, Nanjing, Peoples R China
[5] Jiangsu Univ, Dept Crit Care Med, Affiliated Yixing Hosp, Yixing, Peoples R China
[6] Kunming Univ Sci & Technol Sci & Technol, Fac Life Sci & Technol, Kunming, Yunnan, Peoples R China
[7] St Vincents Hosp, Dept Gastroenterol, Fitzroy, Vic, Australia
[8] Fifth Peoples Hosp Suzhou, Dept Hepatol, Suzhou, Peoples R China
[9] Nanjing Med Univ, Ctr Global Hlth, Sch Publ Hlth, Dept Biostat, Nanjing, Peoples R China
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
direct-acting antivirals; hepatitis C virus; reinfection; relapse; sustained virological response; TERM-FOLLOW-UP; CHRONIC HCV INFECTION; CIRRHOSIS FOLLOWING TREATMENT; PLUS RIBAVIRIN; PEGINTERFERON ALPHA-2A; PEGYLATED INTERFERON; LATE RELAPSE; GENOTYPE; REINFECTION; THERAPY;
D O I
10.1111/liv.14976
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims The risk for hepatitis C virus (HCV) recurrence persists after HCV eradication with direct-acting antivirals (DAAs), particularly in patients with ongoing high-risk behaviours. Our aim was to assess the risk of HCV recurrence (late relapse and/or reinfection) post-sustained virological response (SVR). Methods We searched the literature for studies reporting HCV recurrence rates post-SVR in PubMed, Web of Science and the Cochrane Library. Identified publications were divided into groups based on patient risk for HCV reinfection: low-risk HCV mono-infection, high-risk HCV mono-infection and a human immunodeficiency virus (HIV)/HCV coinfection. The HCV recurrence rate for each study was calculated by using events divided by the person-years of follow-up (PYFU). HCV recurrence was defined as confirmed, detectable HCV RNA post-SVR. Results In the 16 studies of low-risk patients, the pooled recurrence rate was 0.89/1000 PYFU (95% confidence interval [CI], 0.16-2.03). For the 19 studies of high-risk patients, the pooled recurrence rate was 29.37/1000 PYFU (95% CI, 15.54-46.91). For the eight studies of HIV/HCV-coinfected patients, the pooled recurrence rate was 23.25/1000 PYFU (95% CI, 4.24-53.39). The higher pooled estimates of recurrence in the high-risk and HIV/HCV-coinfected populations were predominantly driven by an increase in reinfection rather than late relapse. Conclusions The HCV recurrence risk after achieving SVR with all-oral DAAs therapy is low, and the risk of HCV recurrence in high-risk and HIV/HCV-coinfected populations was driven by an increase in reinfection rather than late relapse.
引用
收藏
页码:2341 / 2357
页数:17
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