Brief Article
Copyright ©2013 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Mar 28, 2013; 19(12): 1943-1952
Published online Mar 28, 2013. doi: 10.3748/wjg.v19.i12.1943
Factors associated with early virological response to peginterferon-α-2a/ribavirin in chronic hepatitis C
Javier García-Samaniego, Miriam Romero, Rafael Granados, Remedios Alemán, Miguel Jorge Juan, Dolores Suárez, Ramón Pérez, Gregorio Castellano, Carlos González-Portela
Javier García-Samaniego, Miriam Romero, Liver Unit, Hospital Carlos III, Centro de Investigación Biómedica en Red de Enfermedades Hepáticas y Digestivas, 28029 Madrid, Spain
Rafael Granados, Department of Gastroenterology, Hospital Universitario de Gran Canaria Dr. Negrín, 35010 Las Palmas de Gran Canaria, Spain
Remedios Alemán, Gastroenterology Service, Hospital Universitario de Canarias, 38320 Tenerife, Spain
Miguel Jorge Juan, Department of Gastroenterology, Hospital Universitario Insular de Gran Canaria, 35016 Las Palmas de Gran Canaria, Spain
Dolores Suárez, Internal Medicine Service, Hospital Arquitecto Marcide, 15405 Ferrol , Spain
Ramón Pérez, Gastroenterology Service, Hospital Central de Asturias, 33006 Oviedo, Spain
Gregorio Castellano, Gastroenterology Service, Hospital 12 de Octubre, 28041 Madrid, Spain
Carlos González-Portela, Gastroenterology Service, Hospital Policlínico de Vigo, 36211 Vigo, Spain
Author contributions: García-Samaniego J and Romero M designed the study and contributed to the interpretation of data; all authors collected data, revised the article critically and approved the final version of the article.
Supported by Roche Farma SA, Spain
Correspondence to: Javier García-Samaniego, MD, Liver Unit, Hospital Carlos III, Centro de Investigación Biómedica en Red de Enfermedades Hepáticas y Digestivas, C/ Sinesio Delgado 10, 28029 Madrid, Spain. javiersamaniego@telefonica.net
Telephone: +34-91-4532510 Fax: +34-91-7336614
Received: September 20, 2012
Revised: December 19, 2012
Accepted: January 5, 2013
Published online: March 28, 2013
Abstract

AIM: To evaluate the impact of sociodemographic/clinical factors on early virological response (EVR) to peginterferon/ribavirin for chronic hepatitis C (CHC) in clinical practice.

METHODS: We conducted a multicenter, cross-sectional, observational study in Hepatology Units of 91 Spanish hospitals. CHC patients treated with peginterferon α-2a plus ribavirin were included. EVR was defined as undetectable hepatitis C virus (HCV)-ribonucleic acid (RNA) or ≥ 2 log HCV-RNA decrease after 12 wk of treatment. A bivariate analysis of sociodemographic and clinical variables associated with EVR was carried out. Independent factors associated with an EVR were analyzed using a multiple regression analysis that included the following baseline demographic and clinical variables: age (≤ 40 years vs > 40 years), gender, race, educational level, marital status and family status, weight, alcohol and tobacco consumption, source of HCV infection, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, and gamma glutamyl transpeptidase (GGT) (≤ 85 IU/mL vs > 85 IU/mL), serum ferritin, serum HCV-RNA concentration (< 400 000 vs≥ 400 000), genotype (1/4 vs 3/4), cirrhotic status and ribavirin dose (800/1000/1200 mg/d).

RESULTS: A total of 1014 patients were included in the study. Mean age of the patients was 44.3 ± 9.8 years, 70% were male, and 97% were Caucasian. The main sources of HCV infection were intravenous drug abuse (25%) and blood transfusion (23%). Seventy-eight percent were infected with HCV genotype 1/4 (68% had genotype 1) and 22% with genotypes 2/3. The HCV-RNA level was > 400 000 IU/mL in 74% of patients. The mean ALT and AST levels were 88.4 ± 69.7 IU/mL and 73.9 ± 64.4 IU/mL, respectively, and mean GGT level was 82 ± 91.6 IU/mL. The mean ferritin level was 266 ± 284.8 μg/L. Only 6.2% of patients presented with cirrhosis. All patients received 180 mg of peginterferon α-2a. The most frequently used ribavirin doses were 1000 mg/d (41%) and 1200 mg/d (41%). The planned treatment duration was 48 wk for 92% of patients with genotype 2/3 and 24 wk for 97% of those with genotype 1/4 (P < 0.001). Seven percent of patients experienced at least one reduction in ribavirin or peginterferon α-2a dose, respectively. Only 2% of patients required a dose reduction of both drugs. Treatment was continued until week 12 in 99% of patients. Treatment compliance was ≥ 80% in 98% of patients. EVR was achieved in 87% of cases (96% vs 83% of patients with genotype 2/3 and 1/4, respectively; P < 0.001). The bivariate analysis showed that patients who failed to achieve EVR were older (P < 0.005), had higher ALT (P < 0.05), AST (P < 0.05), GGT (P < 0.001) and ferritin levels (P < 0.001), a diagnosis of cirrhosis (P < 0.001), and a higher baseline viral load (P < 0.05) than patients reaching an EVR. Age < 40 years [odds ratios (OR): 0.543, 95%CI: 0.373-0.790, P < 0.01], GGT < 85 IU/mL (OR: 3.301, 95%CI: 0.192-0.471, P < 0.001), low ferritin levels (OR: 0.999, 95%CI: 0.998-0.999, P < 0.01) and genotype other than 1/4 (OR: 4.716, 95%CI: 2.010-11.063, P < 0.001) were identified as independent predictors for EVR in the multivariate analysis.

CONCLUSION: CHC patients treated with peginterferon-α-2a/ribavirin in clinical practice show high EVR. Older age, genotype 1/4, and high GGT were associated with lack of EVR.

Keywords: Antiviral therapy, Baseline factors, Early virological response, Peginterferon α-2a, Ribavirin