Monitoring of viral levels during therapy of hepatitis C

被引:148
作者
Davis, GL [1 ]
机构
[1] Baylor Univ, Med Ctr, Hepatol Div, Dallas, TX 75246 USA
关键词
D O I
10.1053/jhep.2002.36798
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Alpha interferon therapy of chronic hepatitis C is typically accompanied by a biphasic decrease in hepatitis C virus (HCV) RNA levels: an initial rapid decline during the first 24 to 48 hours, and a second more gradual decline during the following weeks. The rate of second-phase decline correlates with ultimate response to interferon treatment. Thus, assessment of early virological response (EVR) may predict outcome. Data from 2 large clinical trials of peginterferon and ribavirin were combined and analyzed to determine the optimal definition of an EVR which, if not achieved, was associated with a low likelihood of a sustained virological response (SVR). A fall in HCV RNA level to undetectable or by at least 2 log(10) units after 12 weeks was found to be the optimal definition of an EVR. Among 965 patients, 778 (80%) achieved an EVR by week 12, including all except I patient with genotypes 2 or 3. Among 187 patients without an EVR, only 3 (1.6%) had an SVR. These findings suggest that patients with genotype I who do not achieve an EVR should stop treatment after 12 weeks. Use of an early stopping rule reduces treatment costs by at least 16% and avoids the inconvenience and side effects of treatment in the 19% of patients without an EVR who have little chance of a lasting virological response.
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页码:S145 / S151
页数:7
相关论文
共 27 条
[1]  
Bekkering FC, 1997, HEPATOLOGY, V26, P1691
[2]   Estimation of early hepatitis C viral clearance in patients receiving daily interferon and ribavirin therapy using a mathematical model [J].
Bekkering, FC ;
Stalgis, C ;
McHutchison, JG ;
Brouwer, JT ;
Perelson, AS .
HEPATOLOGY, 2001, 33 (02) :419-423
[3]  
Comanor L, 2001, AM J GASTROENTEROL, V96, P2968, DOI 10.1111/j.1572-0241.2001.04669.x
[4]  
DAVIS GL, 1994, HEPATOLOGY, V19, P1337, DOI 10.1002/hep.1840190603
[5]   TREATMENT OF CHRONIC HEPATITIS-C WITH RECOMBINANT INTERFERON-ALFA - A MULTICENTER RANDOMIZED, CONTROLLED TRIAL [J].
DAVIS, GL ;
BALART, LA ;
SCHIFF, ER ;
LINDSAY, K ;
BODENHEIMER, HC ;
PERRILLO, RP ;
CAREY, W ;
JACOBSON, IM ;
PAYNE, J ;
DIENSTAG, JL ;
VANTHIEL, DH ;
TAMBURRO, C ;
LEFKOWITCH, J ;
ALBRECHT, J ;
MESCHIEVITZ, C ;
ORTEGO, TJ ;
GIBAS, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (22) :1501-1506
[6]  
Ferenci P, 2001, HEPATOLOGY, V34, p351A
[7]   Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. [J].
Fried, MW ;
Shiffman, ML ;
Reddy, KR ;
Smith, C ;
Marinos, G ;
Goncales, FL ;
Haussinger, D ;
Diago, M ;
Carosi, G ;
Dhumeaux, D ;
Craxi, A ;
Lin, A ;
Hoffman, J ;
Yu, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (13) :975-982
[8]   Decline of hepatitis C virus load in serum during the first 24 h after administration of in interferon-beta as a predictor of the efficacy of therapy [J].
Fukutomi, T ;
Nakamuta, M ;
Fukutomi, M ;
Iwao, M ;
Watanabe, H ;
Hiroshige, K ;
Tanabe, Y ;
Nawata, H .
JOURNAL OF HEPATOLOGY, 2001, 34 (01) :100-107
[9]   Peginterferon alfa-2a (40 KD) (pegasys) in combination with ribavirin (RBV): Efficacy and safety results from a phase III, randomized, double-blind, multicentre study examining effect of duration of treatment and RBV dose [J].
Hadziyannis, SJ ;
Cheinquer, H ;
Morgan, T ;
Diago, M ;
Jensen, DM ;
Sette, H ;
Ramadori, G ;
Bodenheimer, HC ;
Marcellin, P ;
Lee, SD ;
Roberts, PJ ;
Ackrill, AM .
JOURNAL OF HEPATOLOGY, 2002, 36 :3-3
[10]  
Herrmann E, 2000, ANTIVIR THER, V5, P85