Review article: current antiviral therapy of chronic hepatitis B

被引:58
作者
Ayoub, W. S. [1 ]
Keeffe, E. B. [1 ]
机构
[1] Stanford Univ, Med Ctr, Div Gastroenterol & Hepatol, Dept Med, Palo Alto, CA 94304 USA
关键词
POSITIVE CHRONIC HEPATITIS; TENOFOVIR DISOPROXIL FUMARATE; HBV-DNA LEVELS; E-ANTIGEN; ADEFOVIR DIPIVOXIL; NATURAL-HISTORY; SURFACE-ANTIGEN; VIRUS INFECTION; HEPATOCELLULAR-CARCINOMA; UNITED-STATES;
D O I
10.1111/j.1365-2036.2011.04869.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background The indications and endpoints for treatment of chronic hepatitis B continue to evolve. The aim of the therapy for chronic hepatitis B is to achieve a long-term continued suppression of the hepatitis B virus (HBV) DNA to prevent disease progression leading to the development of cirrhosis and hepatocellular carcinoma. Aim To summarise current literature on therapy of chronic hepatitis B, with a focus on indications for therapy, preferred treatment options, and management of resistance and partial responders. Methods A systematic review of the literature, with a focus on international guidelines, was performed. Results Seven drugs are licensed for the treatment of chronic hepatitis B in many countries. The selection of a drug with high potency and low rate of resistance is essential to achieve rapid and long-term viral suppression. The prevention of the sequelae of antiviral drug resistance and appropriate management of viral breakthrough are major goals of current management. The addition or change to an antiviral agent that is not cross-resistant is critical to restore suppression of viral replication for patients with breakthrough resistance. Patient adherence to medication is essential to achieve adequate HBV DNA suppression. Conclusions The current treatment strategy of chronic hepatitis B is now standard: initial selection of entecavir, tenofovir, or peginterferon alfa-2a. Future studies are required to determine if combination therapy using two oral agents or peginterferon with an oral agent with a high genetic barrier to resistance might be superior to standard current monotherapy.
引用
收藏
页码:1145 / 1158
页数:14
相关论文
共 103 条
[1]   Review article: current antiviral therapy of chronic hepatitis B [J].
Ayoub, W. S. ;
Keeffe, E. B. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2008, 28 (02) :167-177
[2]  
Berg T, 2010, HEPATOLOGY S, V52, p95A
[3]   Tenofovir Is Effective Alone or With Emtricitabine in Adefovir-Treated Patients With Chronic-Hepatitis B Virus Infection [J].
Berg, Thomas ;
Marcellin, Patrick ;
Zoulim, Fabien ;
Moller, Bernd ;
Trinh, Huy ;
Chan, Sing ;
Suarez, Emilio ;
Lavocat, Fabien ;
Snow-Lampart, Andrea ;
Frederick, David ;
Sorbel, Jeff ;
Borroto-Esoda, Katyna ;
Oldach, David ;
Rousseau, Franck .
GASTROENTEROLOGY, 2010, 139 (04) :1207-+
[4]   Hepatitis B Virus Surface Antigen Levels: A Guide to Sustained Response to peginterferon alfa-2a in HBeAg-Negative Chronic Hepatitis B [J].
Brunetto, Maurizia Rossana ;
Moriconi, Francesco ;
Bonino, Ferruccio ;
Lau, George K. K. ;
Farci, Patrizia ;
Yurdaydin, Cihan ;
Piratvisuth, Teerha ;
Luo, Kanxian ;
Wang, Yuming ;
Hadziyannis, Stephanos ;
Wolf, Eva ;
McCloud, Philip ;
Batrla, Richard ;
Marcellin, Patrick .
HEPATOLOGY, 2009, 49 (04) :1141-1150
[5]   Factors That Predict Response of Patients With Hepatitis B e Antigen-Positive Chronic Hepatitis B to Peginterferon-Alfa [J].
Buster, Erik H. C. J. ;
Hansen, Bettina E. ;
Lau, George K. K. ;
Piratvisuth, Teerha ;
Zeuzem, Stefan ;
Steyerberg, Ewout W. ;
Janssen, Harry L. A. .
GASTROENTEROLOGY, 2009, 137 (06) :2002-2009
[6]   Treatment of hepatitis B e antigen - Positive chronic hepatitis with telbivudine or adefovir [J].
Chan, Henry L. Y. ;
Heathcote, E. Jenny ;
Marcellin, Patrick ;
Lai, Ching-Lung ;
Cho, Mong ;
Moon, Young M. ;
Chao, You-Chen ;
Myers, Robert P. ;
Minuk, Gerald Y. ;
Jeffers, Lennox ;
Sievert, William ;
Bzowej, Natalie ;
Harb, George ;
Kaiser, Ralf ;
Qiao, Xin-Jian ;
Brown, Nathaniel A. .
ANNALS OF INTERNAL MEDICINE, 2007, 147 (11) :745-U14
[7]   A Longitudinal Study on the Natural History of Serum Hepatitis B Surface Antigen Changes in Chronic Hepatitis B [J].
Chan, Henry Lik-Yuen ;
Wong, Vincent Wai-Sun ;
Wong, Grace Lai-Hung ;
Tse, Chi-Hang ;
Chan, Hoi-Yun ;
Sung, Joseph Jao-Yao .
HEPATOLOGY, 2010, 52 (04) :1232-1241
[8]   Long-Term Entecavir Therapy Results in the Reversal of Fibrosis/Cirrhosis and Continued Histological Improvement in Patients with Chronic Hepatitis B [J].
Chang, Ting-Tsung ;
Liaw, Yun-Fan ;
Wu, Shun-Sheng ;
Schiff, Eugene ;
Han, Kwang-Hyub ;
Lai, Ching-Lung ;
Safadi, Rifaat ;
Lee, Samuel S. ;
Halota, Waldemar ;
Goodman, Zachary ;
Chi, Yun-Chan ;
Zhang, Hui ;
Hindes, Robert ;
Iloeje, Uchenna ;
Beebe, Suzanne ;
Kreter, Bruce .
HEPATOLOGY, 2010, 52 (03) :886-893
[9]   Entecavir Treatment for up to 5 Years in Patients with Hepatitis B e Antigen-Positive Chronic Hepatitis B [J].
Chang, Ting-Tsung ;
Lai, Ching-Lung ;
Yoon, Seung Kew ;
Lee, Samuel S. ;
Coelho, Henrique Sergio M. ;
Carrilho, Flair Jose ;
Poordad, Fred ;
Halota, Waldemar ;
Horsmans, Yves ;
Tsai, Naoky ;
Zhang, Hui ;
Tenney, Daniel J. ;
Tamez, Ricardo ;
Iloeje, Uchenna .
HEPATOLOGY, 2010, 51 (02) :422-430
[10]   A comparison of entecavir and lamivudine for HBeAg-positive chronic hepatitis B [J].
Chang, TT ;
Gish, RG ;
de Man, R ;
Gadano, A ;
Sollano, J ;
Chao, YC ;
Lok, AS ;
Han, KH ;
Goodman, Z ;
Zhu, J ;
Cross, A ;
DeHertogh, D ;
Wilber, R ;
Colonno, R ;
Apelian, D .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (10) :1001-1010