Combination therapy of interferon and nucleotide/nucleoside analogues for chronic hepatitis B

被引:58
|
作者
Wong, G. L. -H. [1 ,2 ,3 ]
Wong, V. W. -S. [1 ,2 ,3 ]
Chan, H. L. -Y. [1 ,2 ,3 ]
机构
[1] Chinese Univ Hong Kong, Inst Digest Dis, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, State Key Lab Digest Dis, Hong Kong, Hong Kong, Peoples R China
关键词
adefovir dipivoxil; entecavir; lamivudine; peginterferon; telbivudine; tenofovir; SURFACE-ANTIGEN QUANTIFICATION; RANDOMIZED CONTROLLED-TRIAL; TERM-FOLLOW-UP; LONG-TERM; ALPHA-INTERFERON; PEGYLATED INTERFERON-ALPHA-2B; PEGINTERFERON ALPHA-2A; NUCLEOS(T)IDE ANALOGS; VIROLOGICAL RESPONSE; LAMIVUDINE TREATMENT;
D O I
10.1111/jvh.12341
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Chronic hepatitis B is one of the leading causes of cirrhosis and hepatocellular carcinoma globally. At present, seven drugs, including two interferons and five oral nucleos(t)ide analogues (NAs), have been approved for the treatment of chronic hepatitis B. Interferon works by immunomodulation, but is successful in less than a third of treated patients and is a relatively weak antiviral. NAs directly suppress the hepatitis B virus but have limited durability. Based on current data, combination of NA and interferon results in greater viral suppression but does not translate to off-treatment sustained response. Concomitant or sequential treatment also does not make a difference. Combining telbivudine and interferon also runs the risk of severe peripheral neuropathy. On the other hand, interferon switch or additional therapy in patients well controlled with NAs appears to improve the durability of off-treatment response. This article reviews current data on interferon and NA combination and discusses potential future developments.
引用
收藏
页码:825 / 834
页数:10
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