TY - JOUR
T1 - Long-term outcome and risk stratification in compensated advanced chronic liver disease after HCV-cure
AU - Semmler, Georg
AU - Alonso López, Sonia
AU - Pons, Monica
AU - Lens, Sabela
AU - Dajti, Elton
AU - Griemsmann, Marie
AU - Zanetto, Alberto
AU - Burghart, Lukas
AU - Hametner-Schreil, Stefanie
AU - Hartl, Lukas
AU - Manzano, Marisa
AU - Rodriguez-Tajes, Sergio
AU - Zanaga, Paola
AU - Schwarz, Michael
AU - Gutierrez, María L
AU - Jachs, Mathias
AU - Pocurull, Anna
AU - Polo, Benjamín
AU - Ecker, Dominik
AU - Mateos, Beatriz
AU - Izquierdo, Sonia
AU - Real, Yolanda
AU - Balcar, Lorenz
AU - Carbonell-Asins, Juan A
AU - Gschwantler, Michael
AU - Russo, Francesco P
AU - Azzaroli, Francesco
AU - Maasoumy, Benjamin
AU - Reiberger, Thomas
AU - Forns, Xavier
AU - Genesca, Joan
AU - Bañares, Rafael
AU - Mandorfer, Mattias
N1 - Publisher Copyright:
Copyright © 2024 American Association for the Study of Liver Diseases.
PY - 2025/2/1
Y1 - 2025/2/1
N2 - 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.
AB - 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.
KW - Humans
KW - Male
KW - Female
KW - Middle Aged
KW - Retrospective Studies
KW - Hepatitis C, Chronic/drug therapy
KW - Risk Assessment/methods
KW - Liver Neoplasms/epidemiology
KW - Carcinoma, Hepatocellular/epidemiology
KW - Aged
KW - Incidence
KW - Prognosis
KW - Antiviral Agents/therapeutic use
KW - Algorithms
KW - Liver Cirrhosis/epidemiology
KW - Follow-Up Studies
UR - https://www.scopus.com/pages/publications/85198625694
U2 - 10.1097/HEP.0000000000001005
DO - 10.1097/HEP.0000000000001005
M3 - Journal article
C2 - 39817915
SN - 0270-9139
VL - 81
SP - 609
EP - 624
JO - Hepatology
JF - Hepatology
IS - 2
ER -