End points of therapy in chronic hepatitis B

被引:0
作者
Ahmed, Si Nafa Si [1 ,2 ]
Ecochard, Marie [2 ,3 ]
Zoulim, Fabien [1 ,2 ]
机构
[1] Hop Hotel Dieu, Hosp Civils Lyon, Serv Hepatol & Gastroenterol, F-69002 Lyon, France
[2] INSERM, U871, F-69003 Lyon, France
[3] Univ Lyon 1, Lyon Est IFR62, F-69008 Lyon, France
关键词
antiviral therapy; chronic hepatitis B; clinical end point; clinical trial; natural history; E-ANTIGEN SEROCONVERSION; LONG-TERM EFFICACY; ADEFOVIR DIPIVOXIL; NATURAL-HISTORY; HEPATOCELLULAR-CARCINOMA; LAMIVUDINE TREATMENT; SUSTAINED RESPONSE; ANTIVIRAL THERAPY; VIRUS INFECTION; SERUM HBSAG;
D O I
10.1586/EGH.09.65
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
This review assesses the relevance of the clinical, histological, biochemical and virological end points in the course and outcome of chronic hepatitis B. The pathway and the impact of the variation in these end points are presented, as well as their definitions. The treatment goals are discussed in terms of quality of life and survival. Prevention of the progression of the disease to cirrhosis, decompensated cirrhosis, end-stage liver disease and hepatocellular carcinoma seems to be the best approach to improve survival. As these criteria are long-term end points, easier to use end points assessed in clinical trials as efficacy objectives were also analyzed to determine whether they can be used as accurate surrogate criteria. Results of therapy were then analyzed according to the approved end points and in terms of management of chronic hepatitis B. Finally, an attempt to define new clinical end points is discussed in view of the development of more potent antiviral strategies.
引用
收藏
页码:37 / 49
页数:13
相关论文
共 104 条
  • [1] Ahmed SNS, 2009, EXPERT REV ANTI-INFE, V7, P309, DOI [10.1586/eri.09.10, 10.1586/ERI.09.10]
  • [2] Short statement of the first European consensus conference on the treatment of chronic hepatitis B and C in HIV co-infected patients
    Alberti, A
    Clumeck, N
    Collins, S
    Gerlich, W
    Lundgren, J
    Palù, G
    Reiss, P
    Thiebaut, R
    Weiland, O
    Yazdanpanah, Y
    Zeuzem, S
    [J]. JOURNAL OF HEPATOLOGY, 2005, 42 (05) : 615 - 624
  • [3] Characterization of Occult Hepatitis B Virus Strains in South African Blood Donors
    Allain, Jean-Pierre
    Belkhiri, Dalila
    Vermeulen, Marion
    Crookes, Robert
    Cable, Russell
    Amiri, Azin
    Reddy, Ravi
    Bird, Arthur
    Candotti, Daniel
    [J]. HEPATOLOGY, 2009, 49 (06) : 1868 - 1876
  • [4] Occult hepatitis B virus infection
    Allain, JP
    [J]. TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2004, 11 (01) : 18 - 25
  • [5] Long-term efficacy of interferon alpha-2b and lamivudine in combination compared to lamivudine monotherapy in patients with chronic hepatitis B. An Italian multicenter, randomized trial
    Barbaro, G
    Zechini, F
    Pellicelli, AM
    Francavilla, R
    Scotto, G
    Bacca, D
    Bruno, M
    Babudieri, S
    Annese, M
    Matarazzo, F
    Di Stefano, G
    Barbarini, G
    [J]. JOURNAL OF HEPATOLOGY, 2001, 35 (03) : 406 - 411
  • [6] BEASLEY RP, 1988, CANCER, V61, P1942, DOI 10.1002/1097-0142(19880515)61:10<1942::AID-CNCR2820611003>3.0.CO
  • [7] 2-J
  • [8] BEASLEY RP, 1981, LANCET, V2, P1129
  • [9] SURROGATE END-POINTS - A BASIS FOR A RATIONAL APPROACH
    BOISSEL, JP
    COLLET, JP
    MOLEUR, P
    HAUGH, M
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1992, 43 (03) : 235 - 244
  • [10] Lamivudine treatment can overcome cytotoxic T-cell hyporesponsiveness in chronic hepatitis B: New perspectives for immune therapy
    Boni, C
    Penna, A
    Ogg, GS
    Bertoletti, A
    Pilli, M
    Cavallo, C
    Cavalli, A
    Urbani, S
    Boehme, R
    Panebianco, R
    Fiaccadori, F
    Ferrari, C
    [J]. HEPATOLOGY, 2001, 33 (04) : 963 - 971