Current Management of Hepatitis B in 2016

Abstract

Chronic hepatitis B infection represents a global public health burden, infecting over 240 million persons worldwide. It is associated with significant morbidity and mortality and represents a leading cause for cirrhosis, liver failure, liver cancer, and liver-related death. Current treatment of hepatitis B is focused on identification of patients with active hepatitis within the immune clearance or reactivation phases of chronic infection, for whom antiviral therapy with peg-interferon or nucleos(t)ide analogs are recommended. Seven antiviral agents are currently approved by the US FDA for treatment of chronic hepatitis B, of which three are recommended as first-line agents by major liver societies. As none are associated with virologic cure, the primary objective of antiviral therapy in 2016 is long-term virologic suppression, which is associated with a decreased risk for cirrhosis and hepatocellular carcinoma, and may reverse liver fibrosis or cirrhosis in some patients. Although biochemical improvement in liver enzymes is common, HBeAg seroconversion occurs in only a minority of patients, and HBsAg seroconversion is rare. Due to ongoing deficits along multiple steps of the care cascade, including screening, diagnosis, linkage to care, and antiviral therapy, many patients with chronic hepatitis B remain undiagnosed, lack access to care by specialists with expertise in the management of CHB, or have not been treated with antiviral agents. Future therapies are currently in development with the aim of functional viral cure, which may transform the treatment of CHB and improve liver outcomes.