Chronic hepatitis C virus genotype 6 infection: Response to pegylated interferon and ribavirin

被引:57
作者
Fung, James [1 ]
Lai, Ching-Lung [1 ]
Hung, Ivan [1 ]
Young, John [1 ]
Cheng, Charles [1 ]
Wong, Danny [1 ]
Yuen, Man-Fung [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
来源
JOURNAL OF INFECTIOUS DISEASES | 2008年 / 198卷 / 06期
关键词
D O I
10.1086/591252
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. To date, no study has evaluated pegylated interferon for the treatment of chronic infection with hepatitis C virus (HCV) genotype 6. We aimed to determine the efficacy of pegylated interferon plus ribavirin for treating infection with genotype 6 versus genotype 1. Methods. Forty- two patients chronically infected with HCV (for genotype 1, n = 21; for genotype 6, n = 21) were treated with pegylated interferon alpha-2a (n = 20) or alpha-2b (n = 22) combined with oral ribavirin for 48 weeks. Results. There was no difference between genotypes 1 and 6 in the rates of early virological response (76% vs. 81%; P >.05) and end-of-treatment response (71% vs. 81%; P >.05). Patients infected with genotype 6 had a higher rate of sustained virological response (SVR) than did patients infected with genotype 1 (86% vs. 52%; P = .019). The overall adverse- effects profile was similar in both genotype groups. There was no significant difference in the rate of SVR between patients receiving pegylated interferon alpha- 2a and those receiving alpha- 2b. Multivariate analysis showed that genotype was the only significant factor associated with SVR (P = .039). Conclusions. Treatment with pegylated interferon and ribavirin for 48 weeks resulted in a significantly higher rate of SVR in patients infected with genotype 6 than in those infected with genotype 1. Further studies are required to determine whether lower dosages and 24 weeks of therapy may be sufficient for the treatment of genotype 6 infection.
引用
收藏
页码:808 / 812
页数:5
相关论文
共 21 条
[11]   RELATIONSHIP BETWEEN HEPATITIS-C VIRUS GENOTYPES AND SOURCES OF INFECTION IN PATIENTS WITH CHRONIC HEPATITIS-C [J].
PAWLOTSKY, JM ;
TSAKIRIS, L ;
ROUDOTTHORAVAL, F ;
PELLET, C ;
STUYVER, L ;
DUVAL, J ;
DHUMEAUX, D .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (06) :1607-1610
[12]  
Prescott LE, 1996, J MED VIROL, V50, P168, DOI 10.1002/(SICI)1096-9071(199610)50:2&lt
[13]  
168::AID-JMV10&gt
[14]  
3.0.CO
[15]  
2-I
[16]   Consensus proposals for a unified system of nomenclature of hepatitis C virus genotypes [J].
Simmonds, P ;
Bukh, J ;
Combet, C ;
Deléage, G ;
Enomoto, N ;
Feinstone, S ;
Halfon, P ;
Inchauspé, G ;
Kuiken, C ;
Maertens, G ;
Mizokami, M ;
Murphy, DG ;
Okamoto, H ;
Pawlotsky, JM ;
Penin, FO ;
Sablon, E ;
Tadasu, SI ;
Stuyver, L ;
Thiel, HJ ;
Viazov, S ;
Weiner, A ;
Widell, A .
HEPATOLOGY, 2005, 42 (04) :962-973
[17]   GENOTYPING OF HEPATITIS-C VIRUS IN SOUTH-AFRICA [J].
SMUTS, HM ;
KANNEMEYER, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (06) :1679-1681
[18]  
*WHO, 2000, 164 WHO
[19]   High prevalence of hepatitis C virus genotype 6 among certain risk groups in Hong Kong [J].
Wong, DA ;
Tong, LK ;
Lim, W .
EUROPEAN JOURNAL OF EPIDEMIOLOGY, 1998, 14 (05) :421-426
[20]   Hepatitis C virus genotypes in the United States: Epidemiology, pathogenicity, and response to interferon therapy [J].
Zein, NN ;
Rakela, J ;
Krawitt, EL ;
Reddy, KR ;
Tominaga, T ;
Persing, DH ;
Therneau, TM ;
Gross, JB ;
Poterucha, JJ ;
Gossard, AA ;
Jeffers, LJ ;
Schiff, ER .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (08) :634-+