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丙型肝炎病毒治愈后代偿期晚期慢性肝病的长期预后及风险分层

Long-term outcome and risk stratification in compensated advanced chronic liver disease after HCV-cure.

作者信息

Semmler Georg, Alonso López Sonia, Pons Monica, Lens Sabela, Dajti Elton, Griemsmann Marie, Zanetto Alberto, Burghart Lukas, Hametner-Schreil Stefanie, Hartl Lukas, Manzano Marisa, Rodriguez-Tajes Sergio, Zanaga Paola, Schwarz Michael, Gutierrez María L, Jachs Mathias, Pocurull Anna, Polo Benjamín, Ecker Dominik, Mateos Beatriz, Izquierdo Sonia, Real Yolanda, Balcar Lorenz, Carbonell-Asins Juan A, Gschwantler Michael, Russo Francesco P, Azzaroli Francesco, Maasoumy Benjamin, Reiberger Thomas, Forns Xavier, Genesca Joan, Bañares Rafael, Mandorfer Mattias

机构信息

Department of Medicine III, Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna, Austria.

Vienna Hepatic Hemodynamic Lab, Department of Medicine III, Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna, Austria.

出版信息

Hepatology. 2025 Feb 1;81(2):609-624. doi: 10.1097/HEP.0000000000001005. Epub 2024 Jul 8.

Abstract

BACKGROUND AND AIMS

Around 750,000 patients per year will be cured of HCV infection until 2030. Those with compensated advanced chronic liver disease remain at risk for hepatic decompensation and de novo HCC. Algorithms have been developed to stratify risk early after cure; however, data on long-term outcomes and the prognostic utility of these risk stratification algorithms at later time points are lacking.

APPROACH AND RESULTS

We retrospectively analyzed a cohort of 2335 patients with compensated advanced chronic liver disease (liver stiffness measurement≥10 kPa) who achieved HCV-cure by interferon-free therapies from 15 European centers (median age 60.2±11.9 y, 21.1% obesity, 21.2% diabetes).During a median follow-up of 6 years, first hepatic decompensation occurred in 84 patients (3.6%, incidence rate: 0.74%/y, cumulative incidence at 6 y: 3.2%); 183 (7.8%) patients developed de novo HCC (incidence rate: 1.60%/y, cumulative incidence at 6 y: 8.3%), with both risks being strictly linear over time.Baveno VII criteria to exclude (FU-liver stiffness measurement <12 kPa and follow-up platelet count >150 g/L) or rule-in (FU-liver stiffness measurement ≥25 kPa) clinically significant portal hypertension (CSPH) stratified the risk of hepatic decompensation with proportional hazards. Estimated probability of CSPH discriminated patients developing versus not developing hepatic decompensation in the gray zone (ie, patients meeting none of the above criteria).Published HCC risk stratification algorithms identified high-incidence and low-incidence groups; however, the size of the latter group varied substantially (9.9%-69.1%). A granular "HCC-sustained virologic response" model was developed to inform an individual patient's HCC risk after HCV-cure.

CONCLUSIONS

In patients with compensated advanced chronic liver disease, the risks of hepatic decompensation and HCC remain constant after HCV-cure, even in the long term (>3 y). One-time post-treatment risk stratification based on noninvasive criteria provides important prognostic information that is maintained during long-term follow-up, as the hazards remain proportional over time.

摘要

背景与目的

到2030年,每年约有75万患者将治愈丙型肝炎病毒(HCV)感染。那些代偿期晚期慢性肝病患者仍有肝失代偿和新发肝细胞癌(HCC)的风险。已经开发出算法来在治愈后早期对风险进行分层;然而,缺乏关于长期结局以及这些风险分层算法在后期时间点的预后效用的数据。

方法与结果

我们回顾性分析了来自15个欧洲中心的2335例代偿期晚期慢性肝病患者(肝脏硬度测量值≥10 kPa)的队列,这些患者通过无干扰素疗法实现了HCV治愈(中位年龄60.2±11.9岁,21.1%肥胖,21.2%糖尿病)。在中位随访6年期间,84例患者(3.6%)发生首次肝失代偿(发病率:0.74%/年,6年累积发病率:3.2%);183例(7.8%)患者发生新发HCC(发病率:1.60%/年,6年累积发病率:8.3%),两种风险随时间均呈严格线性关系。用于排除(随访时肝脏硬度测量值<12 kPa且随访血小板计数>150 g/L)或判定(随访时肝脏硬度测量值≥25 kPa)临床显著门静脉高压(CSPH)的Baveno VII标准,以成比例风险对肝失代偿风险进行分层。CSPH的估计概率在灰色区域(即不符合上述任何标准的患者)区分了发生与未发生肝失代偿的患者。已发表的HCC风险分层算法确定了高发病率和低发病率组;然而,后一组的规模差异很大(9.9%-69.1%)。开发了一种精细的“HCV治愈后持续病毒学应答的HCC”模型,以告知个体患者HCV治愈后的HCC风险。

结论

在代偿期晚期慢性肝病患者中,HCV治愈后肝失代偿和HCC的风险即使在长期(>3年)也保持不变。基于非侵入性标准的一次性治疗后风险分层提供了重要的预后信息,在长期随访中仍然有效,因为风险随时间保持成比例关系。

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