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聚乙二醇干扰素α-2a在HBeAg阴性、初治D基因型患者中的疗效及反应预测因素

Efficacy of peginterferon α-2a and predictors of response in HBeAg-negative, genotype D-naive patients.

作者信息

Al-Ashgar Hamad I, Khan Mohammed Q, Aljumah Abdulrahman, Sanai Faisal M, Abdo Ayman A, Dafalla Mutasim M, Fagih Mosa A, Bzeizi Khalid I

机构信息

Section of Gastroenterology, Department of Medicine (MBC-46), King Faisal Specialist Hospital and Research Center, P.O. Box 3354, Riyadh, 11211 Saudi Arabia.

出版信息

Hepatol Int. 2011 Nov 25;6(4):718-26. doi: 10.1007/s12072-011-9319-2. Print 2012 Oct.

Abstract

BACKGROUND

Peginterferon (PEG-IFN) α-2a has been shown to induce a sustained virologic response (SVR) in 20-30% of "hepatitis B e antigen (HBeAg)"-negative patients.

AIM

To determine the safety and efficacy of PEG-IFN α-2a in HBeAg-negative, genotype D-naive patients and to analyze the predictors of response.

METHODS

This prospective, multicenter, open-label, nonrandomized trial was conducted at four hospitals. A total of 35 consecutive HBeAg-negative naive genotype D patients received PEG-IFN α-2a for 48 weeks.

RESULTS

Based on a cutoff of hepatitis B virus (HBV) DNA <400 copies ml(-1), an early virologic response (EVR) at week 12, end of treatment virologic response (ETVR) at week 48, and SVR at week 72 were achieved by 3 (9%), 9 (26%), and 8 patients (23%), respectively. The EVR rate improved to 43%, ETVR to 49%, and SVR to 57%, when a HBV DNA cutoff level of <20,000 copies ml(-1) was used. Pretreatment HBsAg level was not a predictor for SVR on univariate analysis, but correlated with decline in HBV DNA levels at weeks 48 and 72. On multivariate logistic regression analysis, low body weight, high alanine aminotransferase (ALT), low HBV DNA, and low triglyceride levels were identified as baseline predictors of SVR.

CONCLUSION

HBeAg-negative genotype D-naive patients treated with PEG-IFN α-2a achieved SVR in 23 (HBV <400 copies ml(-1)) and 57% (HBV <20,000 copies ml(-1)) of patients, a better response than previously reported that might be related to the absence of drug resistance in these naive patients. Pretreatment predictors of SVR were low body weight, high ALT, low HBV DNA, and low triglycerides.

摘要

背景

聚乙二醇干扰素(PEG-IFN)α-2a已被证明可使20%-30%的“乙肝e抗原(HBeAg)”阴性患者获得持续病毒学应答(SVR)。

目的

确定PEG-IFNα-2a在HBeAg阴性、未感染D基因型的患者中的安全性和疗效,并分析应答的预测因素。

方法

本前瞻性、多中心、开放标签、非随机试验在四家医院进行。共有35例连续的HBeAg阴性、未感染D基因型的初治患者接受PEG-IFNα-2a治疗48周。

结果

以乙肝病毒(HBV)DNA<400拷贝/毫升为界值,第12周的早期病毒学应答(EVR)、第48周的治疗结束时病毒学应答(ETVR)和第72周的SVR分别在3例(9%)、9例(26%)和8例患者(23%)中实现。当采用HBV DNA界值水平<20,000拷贝/毫升时,EVR率提高到43%,ETVR提高到49%,SVR提高到57%。单因素分析显示,治疗前HBsAg水平不是SVR的预测因素,但与第48周和第72周HBV DNA水平的下降相关。多因素logistic回归分析显示,低体重、高丙氨酸氨基转移酶(ALT)、低HBV DNA和低甘油三酯水平是SVR的基线预测因素。

结论

接受PEG-IFNα-2a治疗的HBeAg阴性、未感染D基因型的初治患者中,分别有23%(HBV<400拷贝/毫升)和57%(HBV<20,000拷贝/毫升)的患者获得SVR,这一应答优于先前报道,可能与这些初治患者不存在耐药性有关。SVR的治疗前预测因素为低体重、高ALT、低HBV DNA和低甘油三酯。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e0a/3734594/a58a6cfa4afb/12072_2011_9319_Fig1_HTML.jpg

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