First phase hepatitis c viral kinetics in previous nonresponders patients

被引:19
作者
Cotler, SJ
Layden, JE
Neumann, AU
Jensen, DM
机构
[1] Rush Presbyterian St Lukes Med Ctr, Sect Hepatol, Chicago, IL 60612 USA
[2] Univ Illinois, Chicago, IL 60612 USA
[3] Bar Ilan Univ, Ramat Gan, Israel
关键词
interferon therapy; nonresponder patients; viral kinetics;
D O I
10.1046/j.1365-2893.2003.00401.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
A large proportion of patients fails to respond to treatment for hepatitis C. Initiation of interferon therapy is associated with a rapid first phase decline in viremia, reflecting inhibition of viral production or release from infected cells. We characterized first phase viral kinetics in previous nonresponder patients and compared the antiviral efficacy of interferon in nonresponders to that observed in naive patients. Twenty nonresponders with genotype 1 infection were evaluated. Ten received a single 15 mcg dose of interferon alfacon-1 and ten were given a 30 mcg dose. Viral kinetic data from previously untreated historical control patients with genotype 1 infection who received 9 mcg (n = 12) or 15 mcg (n = 13) of interferon alfacon-1 provided a basis for comparison. Antiviral efficacy was evaluated by calculating the reduction in HCV RNA levels during the first 24 h after interferon administration (log effectiveness). Hepatitis C virus levels decreased exponentially in previous nonresponder patients. Non-responders treated with 30 mcg of interferon alfacon-1 exhibited a greater log drop than non-responders receiving 15 mcg (P = 0.01). The log effectiveness of 15 mcg of interferon alfacon-1 in nonresponders was similar to 9 mcg in naives and was significantly < 15 mcg (P = 0.04) in naive patients. The 30 mcg dose provided similar log effectiveness in nonresponders compared with 15 mcg in naive patients and exceeded the log effectiveness of 9 mcg in previously untreated patients (P = 0.035). Nonresponders who had greater than a 50% decrease in HCV RNA level from baseline at the end of previous treatment had a larger reduction in viral load at 24 h compared with those who had not achieved that level of response with prior therapy (P = 0.04). In conclusion, the log effectiveness of interferon was lower in nonresponders compared with treatment naive patients. The difference in antiviral effectiveness in previous nonresponders was overcome by higher interferon doses.
引用
收藏
页码:43 / 49
页数:7
相关论文
共 32 条
[1]   The prevalence of hepatitis C virus infection in the United States, 1988 through 1994 [J].
Alter, MJ ;
Kruszon-Moran, D ;
Nainan, OV ;
McQuillan, GM ;
Gao, FX ;
Moyer, LA ;
Kaslow, RA ;
Margolis, HS .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (08) :556-562
[2]   EPIDEMIOLOGY OF HEPATITIS-C IN THE WEST [J].
ALTER, MJ .
SEMINARS IN LIVER DISEASE, 1995, 15 (01) :5-14
[3]   Ultrarapid hepatitis C virus clearance by daily high-dose interferon in non-responders to standard therapy [J].
Bekkering, FC ;
Brouwer, JT ;
Leroux-Roels, G ;
Van Vlierberghe, H ;
Elewaut, A ;
Schalm, SW .
JOURNAL OF HEPATOLOGY, 1998, 28 (06) :960-964
[4]  
Bekkering FC, 2000, HEPATOLOGY, V32, p367A
[5]   Interferon and ribavirin for patients with chronic hepatitis C who did not respond to previous interferon therapy: A meta-analysis of controlled and uncontrolled trials [J].
Cheng, SJ ;
Bonis, PAL ;
Lau, J ;
Pham, NQ ;
Wong, JB .
HEPATOLOGY, 2001, 33 (01) :231-240
[6]   Combination of interferon and ribavirin in chronic hepatitis C: Re-treatment of nonresponders to interferon [J].
Di Bisceglie, AM ;
Thompson, J ;
Smith-Wilkaitis, N ;
Brunt, EM ;
Bacon, BR .
HEPATOLOGY, 2001, 33 (03) :704-707
[7]   Re-treatment of chronic hepatitis C with consensus interferon [J].
Heathcote, EJL ;
Keeffe, EB ;
Lee, SS ;
Feinman, SV ;
Tong, MJ ;
Reddy, KR ;
Albert, DG ;
Witt, K ;
Blatt, LM .
HEPATOLOGY, 1998, 27 (04) :1136-1143
[8]   Clinical outcomes after hepatitis C infection from contaminated anti-D immune globulin [J].
Kenny-Walsh, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (16) :1228-1233
[9]   INTERRELATIONSHIP OF BLOOD-TRANSFUSION, NON-A, NON-B HEPATITIS AND HEPATOCELLULAR-CARCINOMA - ANALYSIS BY DETECTION OF ANTIBODY TO HEPATITIS-C VIRUS [J].
KIYOSAWA, K ;
SODEYAMA, T ;
TANAKA, E ;
GIBO, Y ;
YOSHIZAWA, K ;
NAKANO, Y ;
FURUTA, S ;
AKAHANE, Y ;
NISHIOKA, K ;
PURCELL, RH ;
ALTER, HJ .
HEPATOLOGY, 1990, 12 (04) :671-675
[10]  
KOHARA M, 1995, J INFECT DIS, V172, P934, DOI 10.1093/infdis/172.4.934