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恩替卡韦治疗的有效性及病毒学应答的预测因素。

Effectiveness of entecavir treatment and predictive factors for virologic response.

作者信息

Preda Carmen Monica, Baicus Cristian, Negreanu Lucian, Tugui Letitia, Olariu Sandra Viviana, Andrei Adriana, Zambatu Ileana, Diculescu Mircea Mihai

出版信息

Rev Esp Enferm Dig. 2014 May;106(5):305-11.

Abstract

INTRODUCTION

Entecavir (ETV) is a potent inhibitor of hepatitis B virus (HBV) replication. In patients adherent to treatment, virologic remission rates of > 95 % can be maintained with entecavir at 3-5 years.

AIM AND METHODS

A cohort study was performed, including all subjects who received ETV for chronic hepatitis B, in the South- Eastern Romania. We assessed viral response, HBeAg loss and seroconversion, HBsAg loss and seroconversion, biochemical response. Comparison of categorical data was performed by Chi2-test or Fisher´s exact where applicable.

RESULTS

Data from 533 patients were available: predominantly males (64 %), 82.6 % nucleotide naive, 23.1 % HBe-Ag positive, 78.2 % with elevated ALT, 8 % with cirrhosis. The median follow up was 24 months (range 12-48 months). Rate of undetectable HBV DNA increased constantly from year 1 to 3, reaching 91.2 %. Positive predictive factors for virologic response were low score of fibrosis (p-0.006), low level of HBV DNA (p-0.003), while negative predictive factors were: HBe antigen positive status (p-value < 0.001), prior IFN therapy (p 0.015). Virologic rebound was found in 7.8 % (breakthrough in 0.8 %). Rate of HBe Ag loss increases with the therapy duration, reaching 47.83 % in year 3,with two positive predictive factors: Male sex (p = 0.007), and undetectable HBV DNA at 24 weeks (p = 0.002). The percentage of HBs Ag loss was 1.31 %.

CONCLUSIONS

ETV maintained and even increased the high initial response rate (from 78 % to 91.2 %). Low score of fibrosis, low level of HBV DNA, HBe antigen negative status, absence of prior interferon therapy predict a good virologic response. Virologic rebound was found in a higher rate in our population, due probably to a poor drug compliance. Lamivudine-resistant patients usually respond well to ETV, but 15.62 % are non-responders, suspect of Entecavir resistance.

摘要

引言

恩替卡韦(ETV)是一种强效的乙型肝炎病毒(HBV)复制抑制剂。在坚持治疗的患者中,使用恩替卡韦3至5年可维持>95%的病毒学缓解率。

目的与方法

进行了一项队列研究,纳入罗马尼亚东南部所有接受ETV治疗慢性乙型肝炎的患者。我们评估了病毒学应答、HBeAg血清学转换、HBsAg血清学转换及生化应答。分类数据的比较在适用时采用卡方检验或Fisher精确检验。

结果

可得533例患者的数据:主要为男性(64%),82.6%初治核苷类药物,23.1%HBe - Ag阳性,78.2%ALT升高,8%有肝硬化。中位随访时间为24个月(范围12 - 48个月)。HBV DNA检测不到的比例从第1年到第3年持续增加,达到91.2%。病毒学应答的阳性预测因素为纤维化评分低(p = 0.006)、HBV DNA水平低(p = 0.003),而阴性预测因素为:HBe抗原阳性状态(p值<0.001)、既往干扰素治疗(p = 0.015)。7.8%出现病毒学反弹(突破占0.8%)。HBeAg血清学转换率随治疗时间增加,第3年达到47.83%,有两个阳性预测因素:男性(p = 0.007)和24周时HBV DNA检测不到(p = 0.002)。HBsAg血清学转换率为1.31%。

结论

ETV维持甚至提高了较高的初始应答率(从78%提高到91.2%)。纤维化评分低、HBV DNA水平低、HBe抗原阴性状态、无既往干扰素治疗预示着良好的病毒学应答。在我们的人群中病毒学反弹发生率较高,可能归因于药物依从性差。拉米夫定耐药患者通常对ETV反应良好,但15.62%无应答,怀疑恩替卡韦耐药。

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