Interferon therapy in HBeAg positive chronic hepatitis reduces progression to cirrhosis and hepatocellular carcinoma

被引:248
作者
Lin, Shi-Ming
Yu, Ming-Lung
Lee, Chuan-Mo
Chien, Rong-Nan
Sheen, I-Shyan
Chu, Chia-Ming
Liaw, Yun-Fan [1 ]
机构
[1] Chang Gung Univ, Liver Res Unit, Taipei, Taiwan
[2] Chang Gung Mem Hosp, Taipei, Taiwan
[3] Kaohsiung Med Univ & Hosp, Dept Internal Med, Hepatobiliary Div, Kaohsiung, Taiwan
[4] Chang Gung Mem Hosp, Liver Unit, Kaohsiung, Taiwan
关键词
interferon; chronic hepatitis B; hepatocellular carcinoma; cirrhosis; HBeAg seroconversion;
D O I
10.1016/j.jhep.2006.08.021
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The long-term outcomes of interferon-alpha (IFN-alpha) therapy in hepatitis B e antigen (HBeAg) seropositive patients remain controversial. This study was conducted to address this issue. Methods: The long-term outcomes were compared in 233 IFN-treated patients and 233 well-matched untreated controls. Results: The cumulative incidence at the end of 15 years of follow-up (median 6.8 years, range 1.1-16.5 years) in the IFN-treated patients and controls was: HBeAg seroconversion 74.6% vs. 51.7% (P = 0.031); hepatitis B surface antigen (HBsAg) seroclearance 3% vs. 0.4% (P = 0.03); cirrhosis 17.8% vs. 33.7% (P = 0.041); and hepatocellular carcinoma (HCC) 2.7% vs. 12.5% (P = 0.011). Significant reduction of HCC was only observed in patients with pre-existing cirrhosis (P < 0.01). Compared with untreated controls with persistent HBeAg, HBeAg seroconverters in untreated and IFN-treated group showed significantly lower incidence of cirrhosis and HCC (P = 0.003-0.031), while non-seroconverters of IFN-treated group had marginally significant lower incidence of cirrhosis (P = 0.065). Multivariate analysis showed that IFN therapy, HBeAg seroconversion and genotype B HBV infection are independent factors for better long-term outcomes. Conclusions: IFN therapy reduces cirrhosis and HCC development. (c) 2006 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 52
页数:8
相关论文
共 37 条
[1]   Retreatment of chronic hepatitis B e antigen-positive patients with recombinant interferon alfa-2a [J].
Carreño, V ;
Marcellin, P ;
Hadziyannis, S ;
Salmerón, J ;
Diago, M ;
Kitis, GE ;
Vafiadis, I ;
Schalm, SW ;
Zahm, F ;
Manzarbeitia, F ;
Jiménez, FJ ;
Quiroga, JA .
HEPATOLOGY, 1999, 30 (01) :277-282
[2]   Genotype C hepatitis B virus infection is associated with an increased risk of hepatocellular carcinoma [J].
Chan, HLY ;
Hui, AY ;
Wong, ML ;
Tse, AML ;
Hung, LCT ;
Wong, VWS ;
Sung, JJY .
GUT, 2004, 53 (10) :1494-1498
[3]   Determinants for sustained HBeAg response to lamivudine therapy [J].
Chien, RN ;
Yeh, CT ;
Tsai, SL ;
Chu, CM ;
Liaw, YF .
HEPATOLOGY, 2003, 38 (05) :1267-1273
[4]  
Chu CM, 2004, CURR HEPAT REP, V3, P123, DOI DOI 10.1007/S11901-004-0021-X
[5]   PREDNISONE-INTERFERON COMBINATION IN THE TREATMENT OF CHRONIC HEPATITIS-B - DIRECT AND INDIRECT METANALYSIS [J].
COHARD, M ;
POYNARD, T ;
MATHURIN, P ;
ZARSKI, JP .
HEPATOLOGY, 1994, 20 (06) :1390-1398
[6]   Peginterferon α-2a (40 kDa):: an advance in the treatment of hepatitis B e antigen-positive chronic hepatitis B [J].
Cooksley, WGE ;
Piratvisuth, T ;
Lee, SD ;
Mahachai, V ;
Chao, YC ;
Tanwandee, T ;
Chutaputti, A ;
Chang, WY ;
Zahm, FE ;
Pluck, N .
JOURNAL OF VIRAL HEPATITIS, 2003, 10 (04) :298-305
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]  
Ikeda K, 1998, CANCER-AM CANCER SOC, V82, P827, DOI 10.1002/(SICI)1097-0142(19980301)82:5<827::AID-CNCR5>3.0.CO
[9]  
2-G
[10]   Interferon alfa for chronic hepatitis B infection:: Increased efficacy of prolonged treatment [J].
Janssen, HLA ;
Gerken, G ;
Carreño, V ;
Marcellin, P ;
Naoumov, NV ;
Craxi, A ;
Ring-Larsen, H ;
Kitis, G ;
van Hattum, J ;
de Vries, RA ;
Michielsen, PP ;
ten Kate, FJW ;
Hop, WCJ ;
Heijtink, RA ;
Honkoop, P ;
Schalm, SW .
HEPATOLOGY, 1999, 30 (01) :238-243