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

IF 12.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Hepatology Pub Date : 2025-02-01 Epub Date: 2024-07-08 DOI:10.1097/HEP.0000000000001005
Georg Semmler, Sonia Alonso López, Monica Pons, Sabela Lens, Elton Dajti, Marie Griemsmann, Alberto Zanetto, Lukas Burghart, Stefanie Hametner-Schreil, Lukas Hartl, Marisa Manzano, Sergio Rodriguez-Tajes, Paola Zanaga, Michael Schwarz, María L Gutierrez, Mathias Jachs, Anna Pocurull, Benjamín Polo, Dominik Ecker, Beatriz Mateos, Sonia Izquierdo, Yolanda Real, Lorenz Balcar, Juan A Carbonell-Asins, Michael Gschwantler, Francesco P Russo, Francesco Azzaroli, Benjamin Maasoumy, Thomas Reiberger, Xavier Forns, Joan Genesca, Rafael Bañares, Mattias Mandorfer
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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.

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代偿性晚期慢性肝病丙型肝炎治愈后的长期预后和风险分层
背景和目标:到2030年,每年将有大约75万HCV感染者被治愈。代偿性晚期慢性肝病患者仍有肝代偿失代偿和新发HCC的风险。已经开发出了在治愈后早期对风险进行分层的算法;然而,缺乏这些风险分层算法在后期时间点的长期结果和预后效用的数据。方法和结果:我们回顾性分析了来自15个欧洲中心的2335例代偿性晚期慢性肝病(肝硬度测量≥10 kPa)患者,他们通过无干扰素治疗实现了hcv的治愈(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例患者发生首次肝功能失代偿(3.6%,发病率:0.74%/年,6年累计发病率:3.2%);183例(7.8%)患者新发HCC(发病率:1.60%/年,6年累计发病率:8.3%),两种风险随时间严格呈线性关系。排除(fu -肝硬度测量值150 g/L)或常规(fu -肝硬度测量值≥25 kPa)临床显著的门脉高压(CSPH)的Baveno VII标准将肝失代偿风险按比例分层。CSPH的估计概率在灰色地带(即不符合上述标准的患者)区分发生与未发生肝代偿。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,后一组的规模变化很大(9.9%-69.1%)。开发了颗粒状的“HCC持续病毒学反应”模型,以告知个体患者在hcv治愈后的HCC风险。结论:在代偿性晚期慢性肝病患者中,肝失代偿和HCC的风险在hcv治愈后保持不变,即使是长期(bbb30)。基于无创标准的一次性治疗后风险分层提供了重要的预后信息,该信息在长期随访中保持不变,因为风险随时间保持成比例。
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来源期刊
Hepatology
Hepatology 医学-胃肠肝病学
CiteScore
27.50
自引率
3.70%
发文量
609
审稿时长
1 months
期刊介绍: HEPATOLOGY is recognized as the leading publication in the field of liver disease. It features original, peer-reviewed articles covering various aspects of liver structure, function, and disease. The journal's distinguished Editorial Board carefully selects the best articles each month, focusing on topics including immunology, chronic hepatitis, viral hepatitis, cirrhosis, genetic and metabolic liver diseases, liver cancer, and drug metabolism.
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