Entecavir: a potent antiviral with minimal long-term resistance in nucleoside-naive chronic hepatitis B patients

被引:24
作者
Cheng, Pin-Nan [2 ]
Chang, Ting-Tsung [1 ]
机构
[1] Natl Cheng Kung Univ Hosp, Dept Internal Med, Tainan 70428, Taiwan
[2] Natl Cheng Kung Univ, Med Coll & Hosp, Tainan 70101, Taiwan
关键词
ALT; chronic hepatitis B; cirrhosis; HBeAg; HBV DNA; hepatocellular carcinoma; lamivudine-refractory; lamivudine-refractory resistance; nucleoside-naive patients; resistance; seroconversion; viral suppression;
D O I
10.1586/14787210.6.5.569
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Entecavir has demonstrated safety and efficacy in the treatment of chronic hepatitis B infection. It is the prototype for the cyclopentane class of nucleoside/nucleotide chronic hepatitis B antiviral agents. It has a high potency and, due to its structural formula and mechanism of action, entecavir is associated with emergence of minimal resistance in the long-term treatment of nucleoside-naive patients. Research suggests that long-term treatment may be required for chronic hepatitis B patients, especially those who acquire HBV early in life, to achieve maximum viral suppression and improve outcomes. Several recent studies have evaluated the long-term safety, efficacy and development of resistance in nucleoside-naive patients treated with entecavir. Results indicate that the long-term use of entecavir is well tolerated and associated with continuous clinical improvement-with an increasing number of patients achieving undetectable levels of HBV DNA, HBeAg seroconversion and minimal resistance. These data underscore the position of entecavir for first-line therapy and highlight its role in the long-term treatment of chronic hepatits B.
引用
收藏
页码:569 / 579
页数:11
相关论文
共 51 条
[1]  
[Anonymous], HEPATOL INT
[2]   Comprehensive evaluation of hepatitis B virus reverse transcriptase substitutions associated with entecavir resistance [J].
Baldick, Carl J. ;
Tenney, Daniel J. ;
Mazzucco, Charles E. ;
Eggers, Betsy J. ;
Rose, Ronald E. ;
Pokornowski, Kevin A. ;
Yu, Cheng F. ;
Colonno, Richard J. .
HEPATOLOGY, 2008, 47 (05) :1473-1482
[3]   BMS-200475, a novel carbocyclic 2'-deoxyguanosine analog with potent and selective anti-hepatitis B virus activity in vitro [J].
Bisacchi, GS ;
Chao, ST ;
Bachard, C ;
Daris, JP ;
Innaimo, S ;
Jacobs, GA ;
Kocy, O ;
Lapointe, P ;
Martel, A ;
Merchant, Z ;
Slusarchyk, WA ;
Sundeen, JE ;
Young, MG ;
Colonno, R ;
Zahler, R .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1997, 7 (02) :127-132
[4]   Current approaches for treating chronic hepatitis B: when to start, what to start with, and when to stop [J].
Chang, Ting-Tsung ;
Suh, Dong Jin .
HEPATOLOGY INTERNATIONAL, 2008, 2 (Suppl 1) :S19-S27
[5]   A dose-ranging study of the efficacy and tolerability of entecavir in lamivudine-refractory chronic hepatitis B patients [J].
Chang, TT ;
Gish, RG ;
Hadziyannis, SJ ;
Cianciara, J ;
Rizzetto, M ;
Schiff, ER ;
Pastore, G ;
Bacon, BR ;
Poynard, T ;
Joshi, S ;
Klesczewski, KS ;
Thiry, A ;
Rose, RE ;
Colonno, RJ ;
Hindes, RG .
GASTROENTEROLOGY, 2005, 129 (04) :1198-1209
[6]   Four years of lamivudine treatment in Chinese patients with chronic hepatitis B [J].
Chang, TT ;
Lai, CL ;
Chien, RN ;
Guan, R ;
Lim, SG ;
Lee, CM ;
Ng, KY ;
Nicholls, GJ ;
Dent, JC ;
Leung, NW .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2004, 19 (11) :1276-1282
[7]   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
[8]  
CHEN CF, 2008, HEPATOL INT, V2, pA188
[9]   Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level [J].
Chen, CJ ;
Yang, HI ;
Su, J ;
Jen, CL ;
You, SL ;
Lu, SN ;
Huang, GT ;
Iloeje, UH .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (01) :65-73
[10]  
CHEN CJ, 2008, HEPATOL INT, V2, pA208