Peginterferon Plus Ribavirin and Sustained Virological Response in HCV-Related Cirrhosis: Outcomes and Factors Predicting Response

被引:58
|
作者
Fernandez-Rodriguez, Conrado M. [1 ]
Alonso, Sonia [1 ]
Martinez, Stella M. [2 ,3 ]
Forns, Xavier [2 ,3 ]
Sanchez-Tapias, Jose M. [2 ,3 ]
Rincon, Diego [4 ]
Rodriguez-Caravaca, Gil [1 ]
Barcena, Rafael [5 ]
Serra, Miguel A. [6 ]
Romero-Gomez, Manuel [7 ]
Fernandez, Inmaculada [8 ]
Garcia-Samaniego, Javier [9 ]
Fuente, Javier [10 ]
Sola, Ricard [11 ]
Moreno-Otero, Ricardo [12 ]
Planas, Ramon [13 ]
机构
[1] Hosp Univ Fdn Alcorcon, Madrid 28922, Spain
[2] Hosp Clin & Prov, Badalona, Spain
[3] IDIBAPS, Badalona, Spain
[4] Hosp Univ Gregorio Maranon Ciberehd, Madrid, Spain
[5] Hosp Ramon & Cajal, E-28034 Madrid, Spain
[6] Hosp Clin Univ, Valencia, Spain
[7] Hosp Valme Ciberehd, Seville, Spain
[8] Hosp Univ 12 Octubre, Madrid, Spain
[9] Hosp Carlos III Ciberehd, Madrid, Spain
[10] Hosp Miguel Servet, Zaragoza, Spain
[11] Hosp del Mar, Badalona, Spain
[12] Hosp Univ La Princesa, Madrid, Spain
[13] Hosp Badalona Germans Trias & Pujol, Badalona, Spain
关键词
CHRONIC HEPATITIS-C; HEPATOCELLULAR-CARCINOMA; COMPENSATED CIRRHOSIS; ANTIVIRAL THERAPY; INTERFERON; VIRUS; PREVENTION; MANAGEMENT; HISTORY;
D O I
10.1038/ajg.2010.294
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Patients with hepatitis C virus (HCV) cirrhosis are difficult to treat and have a high risk of liver decompensation or hepatocellular carcinoma. We sought to identify factors that could predict treatment response. METHODS: Collaborating centers (n=26) provided data for patients (n=568) with HCV cirrhosis undergoing treatment with peginterferon-alpha plus ribavirin (RBV). Univariate and multivariate analyses were used to evaluate factors predicting treatment outcomes. RESULTS: Sustained viral response (SVR) in naive patients was 30.7%, with no significant differences between centers. Median follow-up was 35 months (range: 1-81). Factors predicting SVR were: non-genotype 1 (odds ratio (OR)=4.183; 95% confidence interval (CI): 2.353-7.438) overall dose and >= 80% of the scheduled time of treatment (OR=3.177; 95% CI: 1.752-5.760); serum.-glutamyl transpeptidase (GGT) <76 IU per ml (OR=4.092; 95% CI: 2.418-6.927); baseline viral load <6 x 10(5) (OR=2.597; 95% CI: 1.583-4.262); absence of ultrasound signs of portal hypertension (OR=2.067; 95% CI: 1.26-3.39). No patient with a HCV-RNA decline <1 log(10) at week 4 achieved SVR. Event-free survival at 5 years was 91% in patients with SVR vs. 59% in non-responders (P<0.001). Overall survival in patients with SVR was 98% vs. 86% in non-responders (P=0.005). Independent factors predicting events were absence of SVR (hazard ratio (HR)=2.66; 95% CI: 1.32-5.54), baseline serum albumin <3.9 g per 100 ml (HR=3.06; 95% CI: 1.81-5.15), presence of esophageal varices on endoscopy (HR=2.489; 95% CI: 1.546-4). Improved outcome was more evident in responders with less advanced disease at baseline. CONCLUSIONS: SVR can be achieved in approximately one-third of patients with HCV-related cirrhosis. SVR independently reduces the likelihood of clinical decompensation and improves survival.
引用
收藏
页码:2164 / 2172
页数:9
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