Suppr超能文献

经 ombitasvir/paritaprevir/ritonavir+dasabuvir+ribavirin 治疗的乙型肝炎相关肝硬化肝细胞癌患者的肝细胞癌复发率。

Recurrence rate of hepatocellular carcinoma in patients with treated hepatocellular carcinoma and hepatitis C virus-associated cirrhosis after ombitasvir/paritaprevir/ritonavir+dasabuvir+ribavirin therapy.

机构信息

Gastroenterology and Hepatology Department, Clinic Fundeni Institute, Bucharest, Romania.

Internal Medicine Department, Colentina Hospital, Bucharest, Romania.

出版信息

United European Gastroenterol J. 2019 Jun;7(5):699-708. doi: 10.1177/2050640619841254. Epub 2019 Mar 29.

Abstract

INTRODUCTION

Recent studies have suggested a higher recurrence rate of hepatocellular carcinoma (HCC) in patients with a history of HCC and hepatitis C virus (HCV)-associated cirrhosis treated with direct-acting antiviral (DAA) agents.

MATERIAL AND METHODS

We conducted a prospective analysis of 24 patients with HCV-associated cirrhosis and treated HCC who received ombitasvir/paritaprevir/ritonavir+dasabuvir+ribavirin for 12 weeks. Prior therapies for HCC included resection (9/24 patients), radiofrequency ablation (RFA) (7/24) and trans-arterial chemoembolization (TACE) (8/24). All patients were eligible for treatment if they had no HCC recurrence 6 months after their last procedure. A control group was defined. All patients were followed every 6 months, with dynamic computed tomography and/or magnetic resonance imaging.

RESULTS

The sustained virological response rate per protocol was 21/24 (87.5%). The study group included 14 (59%) males, median age 64 years (51-77), 50% with associated non-alcoholic steatohepatitis and 24% with Child-Pugh A6 points. HCC recurrence rate/100 patient-years was lower in the DAA-HCC group versus control: 5.5 versus 24.6% patient-years for the resection+RFA group ( = 0.044), respectively, and 18.6 versus 72.7% patient-years for TACE group ( = 0.002). Survival without recurrence was higher in the resection+RFA group (45 compared to 18 months ( < 0.001)) and also in the TACE group (44 compared to 11.5 months ( = 0.002)).

CONCLUSIONS

DAA therapy significantly reduced the recurrence rate of HCC and improved survival without recurrence in patients with treated HCV-associated HCC.

摘要

介绍

最近的研究表明,在接受直接作用抗病毒 (DAA) 药物治疗的患有 HCC 和丙型肝炎病毒 (HCV) 相关肝硬化病史的患者中,HCC 的复发率更高。

材料和方法

我们对 24 例接受 Ombitasvir/Paritaprevir/Ritonavir+Dasabuvir+利巴韦林治疗 12 周的 HCV 相关肝硬化和治疗过的 HCC 患者进行了前瞻性分析。HCC 的先前治疗包括切除术(24 例患者中的 9 例)、射频消融术(RFA)(24 例患者中的 7 例)和经动脉化疗栓塞术(TACE)(24 例患者中的 8 例)。如果他们在最后一次治疗后 6 个月内没有 HCC 复发,则所有患者都有资格接受治疗。定义了对照组。所有患者每 6 个月随访一次,进行动态计算机断层扫描和/或磁共振成像。

结果

按方案的持续病毒学应答率为 21/24(87.5%)。研究组包括 14 名(59%)男性,中位年龄 64 岁(51-77),50%合并非酒精性脂肪性肝炎,24%合并 Child-Pugh A6 分。DAA-HCC 组的 HCC 复发率/100 患者年低于对照组:切除术+RFA 组为 5.5%/100 患者年与 24.6%/100 患者年( = 0.044),TACE 组为 18.6%/100 患者年与 72.7%/100 患者年( = 0.002)。切除术+RFA 组的无复发生存率较高(45 个月对比 18 个月( < 0.001)),TACE 组也较高(44 个月对比 11.5 个月( = 0.002))。

结论

DAA 治疗显著降低了接受治疗的 HCV 相关 HCC 患者的 HCC 复发率,并提高了无复发生存率。

相似文献

3
Ombitasvir/paritaprevir/ritonavir and dasabuvir tablets for hepatitis C virus genotype 1 infection.
Ann Pharmacother. 2015 May;49(5):566-81. doi: 10.1177/1060028015570729. Epub 2015 Feb 13.
6
Paritaprevir/ritonavir/ombitasvir and dasabuvir for the treatment of chronic hepatitis C virus infection.
Expert Opin Pharmacother. 2015;16(18):2835-48. doi: 10.1517/14656566.2015.1114099. Epub 2015 Dec 8.
9
Ombitasvir/paritaprevir/ritonavir+dasabuvir+ribavirin for chronic hepatitis C virus genotype 1b-infected cirrhotics (TURQUOISE-IV).
Eur J Gastroenterol Hepatol. 2018 Sep;30(9):1073-1076. doi: 10.1097/MEG.0000000000001166.

引用本文的文献

2
Assessing the impact of direct-acting antivirals on hepatitis C complications: a systematic review and meta-analysis.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Mar;397(3):1421-1431. doi: 10.1007/s00210-023-02716-x. Epub 2023 Sep 20.
3
Predictors of early and late hepatocellular carcinoma recurrence.
World J Gastroenterol. 2023 Feb 28;29(8):1243-1260. doi: 10.3748/wjg.v29.i8.1243.
5
Timing of DAA Initiation After Curative Treatment and Its Relationship with the Recurrence of HCV-Related HCC.
J Hepatocell Carcinoma. 2020 Dec 1;7:347-360. doi: 10.2147/JHC.S279657. eCollection 2020.
6
Week 2020 Poster Presentations.
United European Gastroenterol J. 2020 Oct;8(8_suppl):144-887. doi: 10.1177/2050640620927345.

本文引用的文献

1
EASL Recommendations on Treatment of Hepatitis C 2018.
J Hepatol. 2018 Aug;69(2):461-511. doi: 10.1016/j.jhep.2018.03.026. Epub 2018 Apr 9.
2
De-novo versus recurrent hepatocellular carcinoma following direct-acting antiviral therapy for hepatitis C virus.
Eur J Gastroenterol Hepatol. 2018 Jan;30(1):39-43. doi: 10.1097/MEG.0000000000001004.
3
Drug Treatment for Chronic Hepatitis C Infection and Cancer Risk.
Dtsch Arztebl Int. 2017 Sep 4;114(35-36):597-602. doi: 10.3238/arztebl.2017.0597.
4
Real-Life Use of 3 Direct-Acting Antiviral Regimen in a Large Cohort of Patients with Genotype-1b HCV Compensated Cirrhosis.
J Gastrointestin Liver Dis. 2017 Sep;26(3):275-281. doi: 10.15403/jgld.2014.1121.263.iac.
6
Direct-Acting Antivirals Decreased Tumor Recurrence After Initial Treatment of Hepatitis C Virus-Related Hepatocellular Carcinoma.
Dig Dis Sci. 2017 Oct;62(10):2932-2942. doi: 10.1007/s10620-017-4739-z. Epub 2017 Sep 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验