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Short-Term Evaluation of The Impact of Sofosbuvir-Based Therapy on Hepatic Fibrosis in Patients with Recurrent HCV Infection Post-Transplant

Research Authors
Ahmed Shawkat Abdelmohsen
Research Journal
مؤتمر الابازل المنعقد فى مدينة نيودلهى بالهند
Research Publisher
NULL
Research Rank
3
Research Vol
NULL
Research Website
NULL
Research Year
2018
Research_Pages
NULL
Research Abstract

Hepatitis C virus (HCV) is a major cause in development of chronic liver disease worldwide. The course of disease in the transplant setting is accelerated whereas up to 20%–40% of patients transplanted for HCV will develop cirrhosis after 5 years, compared to 3%–20% at 20 years in the non-transplant setting. The degree of fibrosis determines the stage of the disease and subsequently development of complications. Liver fibrosis can regress in patients with chronic hepatitis in whom the cause of liver damage is adequately managed, but most studies assessing the benefits of viral eradication were performed in the era of IFN-based therapy and in pre-transplant settings.

Aim
To assess noninvasively the effect of sofosbuvir-based antiviral therapy on liver fibrosis in patients with post-transplant recurrent HCV infection.

Material and Methods

This is a prospective study, in which patients with recurrent HCV infection post-transplant, treated with sofosbuvir plus ribavirin were enrolled. Clinical, biochemical findings (including APRI and FIB-4 scores) and liver stiffness (LS), measured by Fibroscan at baseline and at 3 months after end of therapy, virological data, type of immunosuppression and response to antiviral therapy were evaluated. Patients were further divided into two groups, according to antiviral response.

Results

From August 2014 till January 2016, sixty patients were enrolled, 78.3% were male, 67.8% had genotype 1 and 61.7% received previous HCV treatment. At baseline, 21 patients (35%) had severe fibrosis according to Ishak score. The median time interval from LT was 51 months (5-284), immunosuppressive therapy was tacrolimus based in 78.4%. The median baseline HCV-RNA was 2.341.172 UI/ml (770-52.330.800 UI/ml). SVR was achieved in 43 patients (71.6%). There was significant decrease in LS, FIB-4 and APRI scores in patients who achieved SVR in comparison to those who did not achieve SVR (Median change of LS, FIB-4 and APRI in SVR vs. NSVR group was 4.9 vs. 2.2 (P=0.000 vs. 0.074), 1.06 vs. 0.6 (P=0.000 vs. 0.177) and 0.97 vs. 0.44 (P=0.000 vs. 0.177) respectively). The percentage of the patients with improved LS, FIB-4 and APRI scores in SVR vs. NSVR group was 86% vs. 58.8%, 79.1% vs. 70.5% and 86% vs. 64.7% respectively. Multiple linear regression was done for patients with SVR and it was found that the change in FIB-4 and APRI was significantly associated with pre-treatment levels of AST, GGT, bilirubin, INR and Child Pugh score, while the change in LS was associated only with high pre-treatment LS values.

Conclusion
Eradication of HCV with sofosbuvir-based regimen leads to significant regression in Liver fibrosis, assessed by combined non-invasive tests in post-transplant setting as early as 3 months post-therapy.