Management of Chronic Hepatitis B: New Stopping Rules


Chronic hepatitis B (CHB) treatment is limited by the availability of antiviral agents and the variable response to those agents. Currently, the only approved antiviral agents are Pegylated interferon and nucleos(t)ide analogues. The response to these therapies varies widely between CHB patients. Thus, the patients with non favorable response are ultimately exposed to unnecessary side effects and costs. All current guidelines provide information regarding the time to initiate therapy. However, a clear consensus regarding the predictors of non response and consequently terminating the treatment is still lacking. Many studies that determine the adequacy of the use of predictive markers early in the course of the disease will be reviewed here. During Pegylated interferon therapy, combination of decline in serum HBV DNA and HbsAg levels from baseline at week 12 could generate a solid stopping rule. Using nucleos(t)ide analogues in chronic HbeAg positive patients, the on-treatment HbsAg quantitation at 6 months appears to have a useful role in determining the duration of therapy in patients who achieve HbeAg loss (or seroconversion) during treatment. In chronic HbeAg negative patients, the Asia pacific association for the study of liver (APASL) stopping rules are adequate with proper off-therapy monitoring. Furthermore, the durability of off-therapy response for both classes based on long term follow up studies will be discussed here. Through this review we will present a clear generation of stopping rules to guide the antiviral therapy early enough to predict non-response and shift to other agents. Therefore, adopting a cost effective approach in the treatment of chronic hepatitis B.

Jan 14, 2016
How to Cite
NOUREDDINE, Malak; ISSA, Iyad; MOUCARI, Rami. Management of Chronic Hepatitis B: New Stopping Rules. International Archives of Medicine, [S.l.], v. 8, jan. 2016. ISSN 1755-7682. Available at: <>. Date accessed: 23 sep. 2020. doi:


Chronic hepatitis B virus, management, interferon, entecavir, tenofovir, lamivudine, adefovir