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The role of peginterferon in nucleos(t)ide‐analogue‐treated chronic hepatitis B patients: A review of published literature
Authors:W. Zhang  Q. Xie  Q. Ning  X. Dou  X. Chen  J. Jia  Y. Xie  H. Ren
Affiliation:1. Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China;2. Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China;3. Department of Infectious Diseases, Wuhan Tongji Hospital affiliated to Huazhong Technology University, Tongji Medical College, Wuhan, China;4. Department of Infectious Diseases, Shengjing Hospital of China Medical University, Shenyang, China;5. International Medical Department, Beijing YouAn Hospital, Capital Medical University, Beijing, China;6. Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China;7. Shanghai Roche Pharmaceuticals Ltd, Shanghai, China;8. Department of Infectious Diseases, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China
Abstract:Chronic hepatitis B infection (CHB) causes up to 1.0 million deaths annually. Currently, more than 90% of CHB patients worldwide are receiving indefinite nucleos(t)ide analogue (NA) therapy. New strategies for optimizing hepatitis B surface antigen (HBsAg) loss are required for NA‐treated patients as the majority are unable to achieve HBsAg loss and may require lifelong therapy. In hepatitis B e antigen (HBeAg)‐positive patients, switching from NAs to finite peginterferon (PegIFN) therapy can double HBeAg seroconversion rates. One in five patients who switch to PegIFN can achieve HBsAg loss, whereas patients who continue NA therapy typically do not. In HBeAg‐negative NA‐treated patients, add‐on PegIFN therapy achieves higher, albeit modest, HBsAg loss rates compared with continued NA monotherapy and offers the opportunity for NA‐treated patients to achieve the inactive carrier state. In the absence of curative therapies, PegIFN represents a valuable, finite option for NA‐treated patients who would otherwise require potentially lifelong therapy.
Keywords:chronic hepatitis B  HBsAg loss  nucleos(t)ide analogue  peginterferon
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