Prevention and management of drug resistance for antihepatitis B treatment

被引:48
作者
Yuen, Man-Fung [1 ]
Fung, James [1 ]
Wong, Danny Ka-Ho [1 ]
Lai, Ching-Lung [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
CHRONIC HEPATITIS-B; ADEFOVIR DIPIVOXIL THERAPY; VIRUS POLYMERASE MUTATIONS; TERM LAMIVUDINE THERAPY; HBV DNA LEVEL; COMBINATION THERAPY; YMDD MUTANT; ENTECAVIR RESISTANCE; VIROLOGICAL RESPONSE; DISOPROXIL FUMARATE;
D O I
10.1016/S1473-3099(09)70056-8
中图分类号
R51 [传染病];
学科分类号
100201 [内科学];
摘要
Emergence of drug resistance in antiviral therapy for chronic hepatitis B negates treatment benefits. There is a lower chance for emergence of resistance for drugs with rapid and potent viral suppression and a high genetic barrier for resistant mutations. Measurement of viral load at 24 weeks' treatment to aid decision making is mandatory for patients receiving drugs that are associated with a higher resistance rate. Combination treatment with drugs that belong to different groups is associated with a lower chance of resistance. To ensure better control of viral replication in patients with drug resistance, the addition of another drug without an overlapping resistance profile should be given as early as possible, preferably at the time when genotypic resistance emerges. With such strategies, most patients can be maintained in clinical remission. However, because of the mechanism of viral persistence, research efforts should continue to anticipate and prevent the emergence of multidrug-resistant strains.
引用
收藏
页码:256 / 264
页数:9
相关论文
共 85 条
[1]
Early detection of viral resistance by determination of hepatitis B virus polymerase mutations in patients treated by lamivudine for chronic hepatitis B [J].
Ahmed, SNS ;
Tavan, D ;
Pichoud, C ;
Berby, F ;
Stuyver, L ;
Johnson, M ;
Merle, P ;
Abidi, H ;
Trépo, C ;
Zoulim, F .
HEPATOLOGY, 2000, 32 (05) :1078-1088
[2]
Resistance to adefovir dipivoxil therapy associated with the selection of a novel mutation in the HBV polymerase [J].
Angus, P ;
Vaughan, R ;
Xiong, S ;
Yang, HL ;
Delaney, W ;
Gibbs, C ;
Brosgart, C ;
Colledge, D ;
Edwards, R ;
Ayres, A ;
Bartholomeusz, A ;
Locarnini, S .
GASTROENTEROLOGY, 2003, 125 (02) :292-297
[3]
[Anonymous], HEPATOL INT
[4]
Ninety-six-week efficacy of combination therapy with lamivudine and tenofovir in patients coinfected with HIV-1 and wild-type hepatitis B virus [J].
Bani-Sadr, F ;
Palmer, P ;
Scieux, C ;
Molina, JM .
CLINICAL INFECTIOUS DISEASES, 2004, 39 (07) :1062-1064
[5]
Anti-hepatitis B virus efficacy of tendovir disoproxil fumarate in HIV-infected patients [J].
Benhamou, Y ;
Fleury, H ;
Trimoulet, P ;
Pellegrin, I ;
Urbinelli, R ;
Katlama, C ;
Rozenbaum, W ;
Le Teuff, G ;
Trylesinski, A ;
Piketty, C .
HEPATOLOGY, 2006, 43 (03) :548-555
[6]
Susceptibility to antivirals of a human HBV strain with mutations conferring resistance to both lamivudine and adefovir [J].
Brunelle, MN ;
Jacquard, AC ;
Pichoud, C ;
Durantel, D ;
Carrouée-Durantel, S ;
Villeneuve, JP ;
Trépo, C ;
Zoulim, F .
HEPATOLOGY, 2005, 41 (06) :1391-1398
[7]
Carroúéé-Durantel S, 2008, ANTIVIR THER, V13, P381
[8]
Baseline HBV DNA level is the most important factor associated with virologic breakthrough in chronic hepatitis B treated with lamivudine [J].
Chae, Hee Bok ;
Hann, Hie-Won .
WORLD JOURNAL OF GASTROENTEROLOGY, 2007, 13 (30) :4085-4090
[9]
Virus and transaminase levels determine the emergence of drug resistance during long-term lamivudine therapy in chronic hepatitis B [J].
Chang, ML ;
Chien, RN ;
Yeh, CT ;
Liaw, YF .
JOURNAL OF HEPATOLOGY, 2005, 43 (01) :72-77
[10]
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