| Literature DB >> 27348075 |
Nathalie Ganne-Carrié1,2,3, Richard Layese4, Valérie Bourcier5, Carole Cagnot6, Patrick Marcellin7, Dominique Guyader8, Stanislas Pol9, Dominique Larrey10, Victor de Lédinghen11, Denis Ouzan12, Fabien Zoulim13, Dominique Roulot14,15, Albert Tran16, Jean-Pierre Bronowicki17, Jean-Pierre Zarski18, Ghassan Riachi19, Paul Calès20, Jean-Marie Péron21, Laurent Alric22, Marc Bourlière23, Philippe Mathurin24, Jean-Frédéric Blanc25, Armand Abergel26, Lawrence Serfaty27, Ariane Mallat28, Jean-Didier Grangé29, Pierre Attali30, Yannick Bacq31, Claire Wartelle32, Thông Dao33, Yves Benhamou34, Christophe Pilette35, Christine Silvain36, Christos Christidis37, Dominique Capron38, Brigitte Bernard-Chabert39, David Zucman40, Vincent Di Martino41, Jean-Claude Trinchet5,14,42, Pierre Nahon5,14,42, Françoise Roudot-Thoraval4.
Abstract
UNLABELLED: The aim of this work was to develop an individualized score for predicting hepatocellular carcinoma (HCC) in patients with hepatitis C (HCV)-compensated cirrhosis. Among 1,323 patients with HCV cirrhosis enrolled in the French prospective ANRS CO12 CirVir cohort, 720 and 360 were randomly assigned to training and validation sets, respectively. Cox's multivariate model was used to predict HCC, after which a nomogram was computed to assess individualized risk. During follow-up (median, 51.0 months), 103 and 39 patients developed HCC in the training and validation sets, respectively. Five variables were independently associated with occurrence of HCC: age > 50 years (hazard ratio [HR], 1.94; 95% confidence interval [CI], 1.16; 3.25; P = 0.012); past excessive alcohol intake (HR, 1.55; 95% CI, 1.02; 2.36; P = 0.041); low platelet count (<100 Giga/mm(3) : HR, 2.70; 95% CI, 1.62; 4.51; P < 0.001; [100; 150] Giga/mm(3) : HR, 1.87; 95% CI, 1.10; 3.18; P = 0.021); gamma-glutamyl transpeptidase above the upper limit of normal (HR, 1.96; 95% CI, 1.11; 3.47; P = 0.021); and absence of a sustained virological response during follow-up (HR, 3.02; 95% CI, 1.67; 5.48; P < 0.001). An 11-point risk score was derived from the training cohort and validated in the validation set. Based on this score, the population was stratified into three groups, in which HCC development gradually increased, from 0% to 30.1% at 5 years for patients with the lowest (≤3) and highest (≥8) scores (P < 0.001). Using this score, a nomogram was built enabling individualized prediction of HCC occurrence at 1, 3, and 5 years.Entities:
Mesh:
Year: 2016 PMID: 27348075 DOI: 10.1002/hep.28702
Source DB: PubMed Journal: Hepatology ISSN: 0270-9139 Impact factor: 17.425