An optimistic study was just reported out of the DDW meeting in Chicago regarding a question often discussed on this board – how much reversal in liver damage can one expect if one achieves SVR through treatment?
"The use of interferon or peginterferon for the treatment of patients with hepatitis C can have a dramatic improvement on the histology of the disease, including the disappearance of cirrhosis," summarized Richard Sterling, MD, MSc, Professor of Medicine, Virginia Commonwealth University, and a study co-investigator. "The results of our study show that in patients who respond to treatment, the use of interferon or peginterferon in addition to ribavirin is very effective."
"Researchers conducted a longitudinal cohort study to evaluate the use of IFNTx on liver histology in patients with chronic HCV. Seven hundred and fifty five patients underwent liver biopsy and received a single course of IFNTx or no treatment. Of these patients, 230 were followed for five years without additional treatment (41 patients declined treatment and 189 received IFNTx without obtaining sustained virologic response) before undergoing a repeat liver biopsy. An additional 102 patients who received IFNTx and obtained sustained virologic response (SVR) underwent liver biopsy after five years.
"There were no significant differences in worsening of inflammation or fibrosis scores between those who did not undergo treatment or did not have an SVR. Factors associated with fibrosis progression were change in total inflammation and increase in piecemeal necrosis (interface hepatitis) on second biopsy and presence of interface hepatitis on baseline biopsy. Conversely, the 102 patients who achieved SVR had a significant reduction in fibrosis score; 73 percent of patients who had portal fibrosis on their first biopsy showed no evidence of scarring on the second biopsy, while 20 percent showed no change with treatment. Of the patients with bridging fibrosis on first biopsy (52 percent of the cohort with SVR), 35 percent had no scarring on the second biopsy, 23 percent had portal scarring, 38 percent remained unchanged and 4 percent had cirrhosis, which investigators believe could be a sampling error. For patients with cirrhosis on first biopsy (19 percent of the cohort with SVR), 50 percent had improved on second biopsy — 10 percent had no scarring, 10 percent had portal scarring and 30 percent had improved to bridging fibrosis. African American participants and patients with genotype 1 experienced less sustained virologic responses, which has been shown through other research."
This seems like it provides a good baseline for understanding how much improvement one might expect if one achieves SVR.