Preda Carmen Monica, Baicus Cristian, Negreanu Lucian, Tugui Letitia, Olariu Sandra Viviana, Andrei Adriana, Zambatu Ileana, Diculescu Mircea Mihai
Rev Esp Enferm Dig. 2014 May;106(5):305-11.
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.
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.
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 %.
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.
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。
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。
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%。
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。