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本文引用的文献

1
Chronic hepatitis B in hepatocarcinogenesis.慢性乙型肝炎与肝癌发生
Postgrad Med J. 2006 Aug;82(970):507-15. doi: 10.1136/pgmj.2006.047431.
2
Antiviral options for the treatment of chronic hepatitis B.治疗慢性乙型肝炎的抗病毒选择。
J Antimicrob Chemother. 2006 Jun;57(6):1030-4. doi: 10.1093/jac/dkl123. Epub 2006 Apr 4.
3
Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level.血清乙型肝炎病毒DNA水平生物梯度上肝细胞癌的风险。
JAMA. 2006 Jan 4;295(1):65-73. doi: 10.1001/jama.295.1.65.
4
Hepatitis B virus infection--natural history and clinical consequences.乙型肝炎病毒感染——自然史与临床后果
N Engl J Med. 2004 Mar 11;350(11):1118-29. doi: 10.1056/NEJMra031087.
5
Long-term follow-up of alpha-interferon treatment of patients with chronic hepatitis B.慢性乙型肝炎患者α干扰素治疗的长期随访
Hepatology. 2004 Mar;39(3):804-10. doi: 10.1002/hep.20128.
6
[Relationship between core gene mutations of hepatitis B virus and response to alpha interferon therapy in chronic hepatitis B].[乙型肝炎病毒核心基因突变与慢性乙型肝炎患者对α干扰素治疗反应的关系]
Taehan Kan Hakhoe Chi. 2002 Dec;8(4):381-8.
7
Hepatitis B e antigen and the risk of hepatocellular carcinoma.乙肝e抗原与肝细胞癌风险
N Engl J Med. 2002 Jul 18;347(3):168-74. doi: 10.1056/NEJMoa013215.
8
Interferon and prevention of hepatocellular carcinoma in viral cirrhosis: an evidence-based approach.干扰素与病毒性肝硬化肝细胞癌的预防:循证医学方法
J Hepatol. 2001 Apr;34(4):593-602. doi: 10.1016/s0168-8278(01)00005-8.
9
Long-term beneficial effect of interferon therapy in patients with chronic hepatitis B virus infection.干扰素治疗对慢性乙型肝炎病毒感染患者的长期有益作用。
Hepatology. 1999 Mar;29(3):971-5. doi: 10.1002/hep.510290312.
10
Long-term outcome of hepatitis B e antigen-positive patients with compensated cirrhosis treated with interferon alfa. European Concerted Action on Viral Hepatitis (EUROHEP).接受α干扰素治疗的乙肝e抗原阳性代偿期肝硬化患者的长期预后。欧洲病毒性肝炎协调行动(EUROHEP)。
Hepatology. 1997 Nov;26(5):1338-42. doi: 10.1002/hep.510260536.

与慢性乙型肝炎患者肝癌发生率降低更密切相关的可能是干扰素治疗的生化而非病毒学反应。

Biochemical Rather than Virologic Response to Interferon Therapy may be More Closely Associated with Decrease of Hepatocellular Carcinoma Incidence in Patients with Chronic Hepatitis B.

机构信息

Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Gut Liver. 2007 Jun;1(1):49-55. doi: 10.5009/gnl.2007.1.1.49. Epub 2007 Jun 30.

DOI:10.5009/gnl.2007.1.1.49
PMID:20485658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2871650/
Abstract

BACKGROUND/AIMS: The authors examined whether the response to interferon (IFN) therapy can affect the development of hepatocellular carcinoma (HCC) in chronic hepatitis B (CHB) patients.

METHODS

Out of 353 biopsy-proven CHB patients, 229 (65%) were treated with IFN-alpha for 6 to 12 months. They were followed for a median period of 75 months (range, 6-120). In patients treated with IFN, biochemical and virologic responses were evaluated at the end of treatment (EOT). The cumulative incidence rates of HCC were calculated and analyzed in relation to baseline characteristics as well as biochemical and virologic responses to IFN therapy.

RESULTS

The overall cumulative incidence of HCC was 0%, 0.8%, 3.7% and 5.5% at 3, 5, 7 and 8 years, respectively. Age, serum AFP levels and the stage of fibrosis were significantly associated with the occurrence of HCC. As a whole, IFN therapy did not affect the occurrence of HCC. Among the patients treated with IFN, biochemical responders had low HCC incidence rates compared with non-responders (p=0.018). However, the HCC incidence rates of virologic responders were not different from non-responders (p=0.203).

CONCLUSIONS

Biochemical rather than virologic response to IFN therapy may be more closely associated with decrease of HCC incidence in CHB patients.

摘要

背景/目的:作者研究了干扰素(IFN)治疗的应答是否会影响慢性乙型肝炎(CHB)患者发生肝细胞癌(HCC)。

方法

353 例经活检证实的 CHB 患者中,有 229 例(65%)接受 IFN-α治疗 6-12 个月。中位随访时间为 75 个月(范围 6-120 个月)。在接受 IFN 治疗的患者中,在治疗结束时(EOT)评估了生化和病毒学应答。根据基线特征以及对 IFN 治疗的生化和病毒学应答,计算并分析 HCC 的累积发生率。

结果

总体而言,HCC 的累积发生率分别为 0%、0.8%、3.7%和 5.5%,在 3、5、7 和 8 年时。年龄、血清 AFP 水平和纤维化分期与 HCC 的发生显著相关。整体而言,IFN 治疗并未影响 HCC 的发生。在接受 IFN 治疗的患者中,生化应答者 HCC 的发生率低于无应答者(p=0.018)。但是,病毒学应答者的 HCC 发生率与无应答者没有差异(p=0.203)。

结论

IFN 治疗的生化应答而非病毒学应答可能与 CHB 患者 HCC 发生率的降低更密切相关。