Meta-analysis: treatment of hepatitis B infection reduces risk of hepatocellular carcinoma

被引:304
作者
Sung, J. J. Y. [1 ]
Tsoi, K. K. F. [1 ]
Wong, V. W. S. [1 ]
Li, K. C. T. [1 ]
Chan, H. L. Y. [1 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Inst Digest Dis, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China
关键词
D O I
10.1111/j.1365-2036.2008.03816.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Chronic hepatitis B (CHB) infection leads to development of hepatocellular carcinoma (HCC), but the effects of treatment in preventing HCC are not clear. Aim To study the effects of interferon (IFN) or nucleoside/tide analogue (NA) on the risk of developing HCC in CHB patients. Methods Randomized trials, case-control and cohort studies were retrieved from five electronic databases and international conferences over the past 10 years. Relative risks (RRs) of HCC with or without treatment were studied. Results Twelve studies (n = 2742) enrolling patients treated by IFN vs. control showed that the risk of HCC after treatment was reduced by 34% (RR: 0.66, 95% CI: 0.48-0.89). Benefit is more significant among patients with early cirrhosis than among those without cirrhosis. Five studies (n = 2289) compared patients treated by NA with control. The risk of HCC after treatment was reduced by 78% (RR: 0.22, 95% CI: 0.10-0.50). HBeAg-positive patients showed more significantly reduced HCC risk with treatment. Patients without cirrhosis benefited more from NA than those with cirrhosis. Resistance to NA has obviated the benefit of the treatment. Conclusions IFN or NA treatment significantly reduces risk of HCC. While IFN benefited patients with cirrhosis, NA benefited patients with no cirrhosis and HBeAg-positive CHB infection.
引用
收藏
页码:1067 / 1077
页数:11
相关论文
共 44 条
[1]  
BEASLEY RP, 1981, LANCET, V2, P1129
[2]  
Benvegnù L, 1998, CANCER-AM CANCER SOC, V83, P901, DOI 10.1002/(SICI)1097-0142(19980901)83:5<901::AID-CNCR15>3.0.CO
[3]  
2-Z
[4]  
Brunetto MR, 1998, LANCET, V351, P1535
[5]   High viral load and hepatitis B virus subgenotype Ce are associated with increased risk of hepatocellular carcinoma [J].
Chan, Henry Lik-Yuen ;
Tse, Chi-Hang ;
Mo, Frankie ;
Koh, Jane ;
Wong, Vincent Wai-Sun ;
Wong, Grace Lai-Hung ;
Chan, Stephen Lam ;
Yeo, Winnie ;
Sung, Joseph Jao-Yiu ;
Mok, Tony Shu-Kam .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (02) :177-182
[6]   Epidemiological and virological characteristics of 2 subgroups of hepatitis B virus genotype C [J].
Chan, HLY ;
Tsui, SKW ;
Tse, CH ;
Ng, EYT ;
Au, TCC ;
Yuen, L ;
Bartholomeusz, A ;
Leung, KS ;
Lee, KH ;
Locarnini, S ;
Sung, JJY .
JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (12) :2022-2032
[7]   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
[8]   Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level [J].
Chen, CJ ;
Yang, HI ;
Su, J ;
Jen, CL ;
You, SL ;
Lu, SN ;
Huang, GT ;
Iloeje, UH .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (01) :65-73
[9]  
Chien R. N., 1993, Journal of Hepatology, V18, pS24
[10]   The long-term course of chronic hepatitis B [J].
Di Marco, V ;
Lo Iacono, O ;
Cammà, C ;
Vaccaro, A ;
Giunta, M ;
Martorana, G ;
Fuschi, P ;
Almasio, PL ;
Craxì, A .
HEPATOLOGY, 1999, 30 (01) :257-264