icon-folder.gif   Conference Reports for NATAP  
 
  38th Annual Meeting of the European Association for the Study of the Liver
 
Istanbul, Turkey. March 28-April 1, 2003
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PREDICTORS OF VIROLOGIC RESPONSE IN COMBINATION THERAPY WITH INTERFERON (IFN) ALFA 2B PLUS RIBAVIRIN OF RECURRENT HEPATITIS C AFTER LIVER TRANSPLANTATION (LT)
 
 
  B. Lavezzo*, 1 A. Franchello, 2 A. Smedile, 1 D. Cocchis, 2 E. David, 3 A. Barbui, 4 A. Ottobrelli, 1 M. Fadda, 5 A. Brunati, 2 M. Salizzoni, 2 M. Rizzetto, 1 *Presenting Author 1Dept Of Gastroenterology, 2Dept Of Liver Transplant Surgery, 3Dept Of Pathology Division, 4Dept Of Virology Division, 5Dept Of Clinical Nutrition Service, Molinette Hospital, Turin, Italy
 
Background: combination treatment (CT) with IFN plus ribavirin is efficacious in small group of patients (pts) with recurrent hepatitis C after LT. Predictor factors of response are lacking. Aim: to evaluate pre-treatment predictors of virologic response (negative HCV-RNA by PCR, Monitor Roche) at end of treatment (ETVR) and at 6 months (mo) of follow-up (SVR) in pts treated with CT for recurrent hepatitis C. Methods: we evaluated 108 pts, mean age 53 yr (29-65), 77% males76% genotype 1, with recurrent hepatitis C after LT, histology at baseline: 20 pts acute hepatitis, 88 pts chronic hepatitis with mean grading score of 5/18 (4-11) and mean staging score 2/6 (1-5). They were treated with IFN alfa 2b 3 MU x 3 weekly plus ribavirin 800 mg/die for 6 or 12 mo. Median time LT to treatment was 10 mo (2-86) Immunosuppressive therapy was cyclosporine in 63%, FK in 37% of pts. Mean ALT levels pre-treatment was 238 UI/L (50-1000), mean HCV-RNA level 38 MEq/ml (0, 7-120). Age, gender, immunosuppression, baseline ALT and HCV-RNA levels, histological grading and staging pre-treatment duration of therapy, time interval from LT to start of therapy, genotype were evaluated by linear multivariate regression analysis. Results: ETVR was obtained in 29, 6% of pts, SVR in 23%. HCV genotype non-1 responded better than genotype 1 (SVR 46% vs 16%, p: 0, 001). Age and baseline HCV-RNA were predictors of ETVR (p < 0.05), but not SVR (age p: 0, 07). Duration of therapy was correlated with SVR, but virologic relapse occurred only in genotype-1 pts. In relapsed pts serum HCV-RNA became negative just before the end of therapy. Conclusions: in LT genotype non-1 is predictor of SVR. In genotype-1 duration of therapy should be personalized to obtain a better and stable efficacy of treatment.