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Prediction of hepatocellular carcinoma in Hepatitis C patients with advanced fibrosis after sustained virologic response - 06/07/22

Doi : 10.1016/j.clinre.2022.101923 
Jessica Azzi a, Céline Dorival a, Carole Cagnot b, Hélène Fontaine c, Clovis Lusivika-Nzinga a, Vincent Leroy d, Victor De Ledinghen e, Albert Tran f, g, h, Fabien Zoulim i, Laurent Alric j, Jérôme Gournay k, Jean-Pierre Bronowicki l, Thomas Decaens m, Ghassan Riachi n, Nabiel Mikhail o, p, Reham Soliman o, q, Gamal Shiha o, r, Stanislas Pol c, s, Fabrice Carrat a, t, Nathalie Ganne-Carrié u, v, w,
for the

ANRS-AFEF Hepather Study group

a Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France 
b ANRS (France Recherche Nord & Sud Sida-HIV Hépatites), Unit for Basic and Clinical Research on Viral Hepatitis, Paris, France 
c AP-HP, Hôpital Cochin, Unité d'Hépatologie, Paris, France 
d Department of Hepatology and Gastroenterology, Hôpital Henri Mondor, AP-HP, Université Paris-Est, INSERM U955, Créteil, France 
e Hepatology Unit Hôpital Haut-Lévêque, Pessac, INSERM U1053, Université Bordeaux Segalen, Bordeaux, France 
f Université Côte d'Azur, Nice, France 
g CHU de Nice, Digestive Center, Nice, France 
h INSERM, U1065, C3M, Team 8 « Chronic liver diseases associated with obesity and alcohol », Nice, France 
i Department of Hepatology, Hospices Civils de Lyon, INSERM U1052, Université de Lyon, Lyon, France 
j Department of Internal Medicine and Digestive Diseases, CHU Purpan, UMR 152 Pharma Dev, IRD Toulouse 3 University, France 
k Gastroenterology and Hepatology Department, Institut des Maladies de l'Appareil Digestif, University Hospital of Nantes, Nantes, France 
l Inserm U1254 and Department of Hepato-Gastroenterology, University Hospital of Nancy Brabois, Université de Lorraine, Vandoeuvre-les-Nancy, France 
m Department of Hepatology and Gastroenterology, CHU Grenoble-Alpes, Université Grenoble-Alpes, Institute for Advanced Biosciences INSERM U1209, Grenoble, France 
n Department of Hepatology and Gastroenterology, CHU Charles Nicolle, Rouen, France 
o Egyptian Liver Research Institute and Hospital (ELRIAH), Mansoura, Egypt 
p Biostatistics and Cancer Epidemiology Department, South Egypt Cancer Institute, Assiut University, Assuit, Egypt 
q Tropical Medicine Department, Faculty of Medicine, Port Said University, Port Said, Egypt 
r Hepatology and Gastroenterology Unit, Internal Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt 
s Université de Paris, INSERM U1223 and USM-20, Institut Pasteur, Paris, France 
t AP-HP, Sorbonne Université, Hôpital Saint-Antoine, Santé Publique, Paris, France 
u AP-HP, Hôpitaux Universitaires Paris Seine Saint-Denis, APHP, Liver Unit, Bobigny, France 
v Université Sorbonne Paris Nord, Bobigny, France 
w Inserm, UMR-1138 « Functional Genomics of solid tumors », Centre de Recherche des Cordeliers, Université de Paris, France 

Corresponding author at: Service d'hépatologie, Hôpital Avicenne, 125 rue de Stalingrad, 93000 Bobigny, France.Service d'hépatologieHôpital Avicenne125 rue de StalingradBobigny93000France

Highlights

Among patients with HCV-SVR achieved with DAAs, the main independent associated factors with HCC were cirrhosis, male gender, advanced age, and genotype 3 infection.
Risk factors of HCC formed a performant score for predicting short-term risk of HCC in these patients.
This practical tool can be easily assessed in clinical practice, and can help identifying high-risk subgroup of patients in which screening for HCC would be cost-effective.

Il testo completo di questo articolo è disponibile in PDF.

Abstract

Background & Aims

Prediction of hepatocellular carcinoma (HCC) occurrence in patients with chronic hepatitis C (HCV) who achieved a sustained virological response (SVR) after direct acting antivirals (DAAs) remains challenging.

Methods

Among HCC-free HCV patients with advanced fibrosis enrolled in the ANRS CO22 HEPATHER cohort who achieved SVR 12 weeks after treatment with DAAs, HCC predictive models were developed using Cox multivariable regression. The derived score was externally validated in a large Egyptian cohort. Our main outcome was the HCC-free survival.

Results

During follow-up (median 3.05 years), 153 out of 3531 patients developed a HCC. Main variables associated with HCC occurrence were: male gender, HCV genotype 3, esophageal varices, albumin < 40 g/L, total bilirubin >11 µmol/L and hypercholesterolemia before DAA initiation, together with age > 58 years, FIB-4 index ≥3.25 evaluated at SVR. A score was established allowing the stratification of patients by high (score ≥ 12/22), intermediate (7 ≤ score <12) and low risk of HCC (score < 7/22) with 3-yrs HCC incidence of 18.96%, 5.50% and 1.65%, respectively. The integrated time‐dependent area under the ROC curve (i-AUC) was 0.76 in our patients and 0.61 in the validation cohort.

Conclusion

The externally validated HEPATHER HCC score has good short-term predictive performance in HCV- patients who achieved SVR12 after DAAs allowing to identify high-risk patients in whom HCC screening may be cost-effective and low-risk patients in whom HCC screening may be superfluous in the first 3 years after SVR.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Hepatitis C virus, HCC, Risk factors, Risk score

Abbreviations : AFP, ALT, AST, AUC, CI, DAA, GGT, HBV, HCV, HCC, HR, IDI, IQR, NRI, OS, SVR


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Vol 46 - N° 6

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