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聚乙二醇干扰素联合利巴韦林治疗后获得持续病毒学应答的 HCV 患者的长期随访。

Long-term follow-up of HCV patients with sustained virological response after treatment with pegylated interferon plus ribavirin.

机构信息

Center of Infectious Diseases, West China Hospital of Sichuan University, Chengdu 610041, China.

Center of Infectious Diseases, West China Hospital of Sichuan University, Chengdu 610041, China.

出版信息

Hepatobiliary Pancreat Dis Int. 2021 Apr;20(2):137-141. doi: 10.1016/j.hbpd.2020.02.004. Epub 2020 Feb 21.

DOI:10.1016/j.hbpd.2020.02.004
PMID:32146076
Abstract

BACKGROUND

The progress of liver diseases may not stop after viral eradication. This study aimed to provide data on long-term prognosis of patients with hepatitis C virus (HCV) infection who underwent pegylated interferon plus ribavirin (PR) regimen and achieved a sustained virological response 24 weeks post-treatment (SVR24).

METHODS

Responders to the PR regimen in our hospital from January 2011 to June 2014 were enrolled and prospectively followed up. Baseline characteristics were profiled. The incidence of hepatocellular carcinoma (HCC), progression of liver disease (increase in liver stiffness or occurrence of decompensated complication), and HCV recurrence was all monitored. The accumulative and annualized incidence rates (AIRs) of these adverse events were analyzed, and the risk factors were also examined.

RESULTS

In total, 151 patients reached a median follow-up time of 103 weeks. Among them, two had an incidence of HCC during the surveillance with AIR of 0.68% (95% CI: 0.00-1.63%). Six patients showed progression of liver disease with AIR of 2.05% (95% CI: 0.42%-3.68%). Three patients who had risky behaviors encountered HCV reinfection. The cirrhotic patients faced higher risk of poor prognosis than non-cirrhotic patients, including HCC and progression of liver disease (AIR: 6.17% vs. 1.42%, P = 0.039).

CONCLUSIONS

The incidence of HCC and progression of liver disease was evident in PR responders during the long-term follow-up period, but the risk level was low. Cirrhotic responders were more vulnerable to develop HCC post SVR24 compared with non-cirrhotic ones. HCV recurrence was rare in responders with SVR24 who had corrected their risky behaviors.

摘要

背景

肝脏疾病的进展在病毒清除后可能不会停止。本研究旨在为接受聚乙二醇干扰素加利巴韦林(PR)方案治疗并在治疗后 24 周达到持续病毒学应答(SVR24)的丙型肝炎病毒(HCV)感染患者提供长期预后数据。

方法

纳入我院 2011 年 1 月至 2014 年 6 月接受 PR 方案治疗并达到应答的患者,并进行前瞻性随访。分析其基线特征。监测肝细胞癌(HCC)的发生、肝病进展(肝硬度增加或失代偿性并发症发生)以及 HCV 复发情况。分析这些不良事件的累积发生率(AIR)和相关危险因素。

结果

共 151 例患者中位随访时间为 103 周。其中,2 例在监测期间发生 HCC,AIR 为 0.68%(95%CI:0.00-1.63%)。6 例患者出现肝病进展,AIR 为 2.05%(95%CI:0.42%-3.68%)。3 例有高危行为的患者出现 HCV 再感染。与非肝硬化患者相比,肝硬化患者的预后不良风险更高,包括 HCC 和肝病进展(AIR:6.17%比 1.42%,P=0.039)。

结论

在长期随访期间,PR 应答者的 HCC 和肝病进展发生率显著,但风险水平较低。与非肝硬化患者相比,SVR24 后的肝硬化应答者发生 HCC 的风险更高。对于 SVR24 且已纠正高危行为的应答者,HCV 复发罕见。

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