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直接抗病毒药物治疗与晚期/失代偿期肝硬化的长期肝功能:HCV-TARGET 队列的真实世界经验。

DAA therapy and long-term hepatic function in advanced/decompensated cirrhosis: Real-world experience from HCV-TARGET cohort.

机构信息

Columbia University, New York, NY.

Division of Gastroenterology, Hepatology, and Nutrition, University of Florida, Gainesville, FL.

出版信息

J Hepatol. 2020 Sep;73(3):540-548. doi: 10.1016/j.jhep.2020.03.031. Epub 2020 Mar 31.

Abstract

BACKGROUND & AIMS: Direct-acting antiviral (DAA) therapy is used in patients with HCV-related decompensated cirrhosis with the expectation of improving hepatic function. However, little is known about the long-term hepatic benefit of successful antiviral treatment.

METHODS

Patients with advanced/decompensated cirrhosis (model for end-stage liver disease [MELD] ≥10), in whom NS5A-containing DAA therapy was initiated prior to September 2018, were included (from the HCV-TARGET cohort). Treatment outcomes and the impact of treatment on short-term and long-term hepatic function were examined.

RESULTS

A total of 642 patients were analyzed. The mean age was 60 years, 68% were male. The median baseline MELD was 12 (range 10-39) and 64% had prior decompensation. Among patients with available virologic outcomes, 90.5% achieved a sustained virologic response at 12 weeks (SVR12). Eighty (24%) patients achieved a clinically significant decrease in MELD by ≥3 points during short-term follow-up (9-26 weeks after the end of treatment). However, in long-term follow-up (median of 4 years after treatment), mean changes in MELD (-0.30 points), total bilirubin (+0.23 mg/dl) and albumin (+0.36 g/dl) were marginal. Fifty-one patients died and 22 underwent liver transplant. In long-term follow-up, a clinically meaningful decrease in MELD of ≥3 occurred in 29% and a final MELD score of <10 was achieved in 25%.

CONCLUSION

In a large real-world experience of patients with advanced/decompensated HCV-related cirrhosis treated with DAAs, there were only marginal improvements in MELD, total bilirubin, or albumin at long-term follow-up (after achieving SVR12). These patients may remain at high risk of decompensation and must continue to be closely monitored. CLINICALTRIALS.GOV: NCT01474811.

LAY SUMMARY

Hepatitis C virus infection can now be cured with medications, even in patients who have advanced scarring of the liver (cirrhosis). In this study, we evaluated whether liver function improves or deteriorates in the long-term, following successful treatment of hepatitis C in patients with cirrhosis. We found that overall liver function was relatively stable with only 29% of patients achieving a clinically meaningful improvement in liver function, and we therefore believe that these patients require ongoing monitoring.

摘要

背景与目的

直接作用抗病毒(DAA)疗法用于治疗丙型肝炎相关失代偿性肝硬化患者,以期改善肝功能。然而,对于成功抗病毒治疗的长期肝脏获益知之甚少。

方法

纳入了在 2018 年 9 月之前开始接受含 NS5A 的 DAA 治疗的晚期/失代偿性肝硬化(终末期肝病模型 [MELD]≥10)患者(来自 HCV-TARGET 队列)。检查了治疗结局以及治疗对短期和长期肝功能的影响。

结果

共分析了 642 例患者。平均年龄为 60 岁,68%为男性。中位基线 MELD 为 12(范围 10-39),64%有既往失代偿。在有可用病毒学结局的患者中,90.5%在 12 周时达到持续病毒学应答(SVR12)。80(24%)例患者在短期随访(治疗结束后 9-26 周)期间,MELD 降低≥3 分。然而,在长期随访(治疗后中位数为 4 年)中,MELD(-0.30 分)、总胆红素(+0.23mg/dl)和白蛋白(+0.36g/dl)的平均变化不大。51 例患者死亡,22 例接受了肝移植。在长期随访中,29%的患者 MELD 显著降低≥3,25%的患者最终 MELD 评分<10。

结论

在接受 DAA 治疗的晚期/失代偿性丙型肝炎相关肝硬化患者的大型真实世界经验中,在长期随访(达到 SVR12 后)时,MELD、总胆红素或白蛋白仅略有改善。这些患者仍有很高的失代偿风险,必须继续密切监测。CLINICALTRIALS.GOV:NCT01474811。

患者教育

丙型肝炎病毒感染现在可以用药物治愈,即使是在肝脏有严重瘢痕(肝硬化)的患者中。在这项研究中,我们评估了在成功治疗肝硬化患者的丙型肝炎后,长期肝功能是否会改善或恶化。我们发现,整体肝功能相对稳定,只有 29%的患者肝功能有显著改善,因此我们认为这些患者需要持续监测。

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