Vassiliadis Themistoklis, Tziomalos Konstantinos, Patsiaoura Kalliopi, Zagris Thomas, Giouleme Olga, Soufleris Konstantinos, Grammatikos Nikolaos, Theodoropoulos Konstantinos, Mpoumponaris Alexandros, Dona Konstantina, Zezos Petros, Nikolaidis Nikolaos, Orfanou-Koumerkeridou Eleni, Balaska Aikaterini, Eugenidis Nikolaos
2nd Propaedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, Hippokration Hospital, Thessaloniki, Greece.
J Gastroenterol Hepatol. 2007 Oct;22(10):1582-8. doi: 10.1111/j.1440-1746.2007.05103.x. Epub 2007 Aug 7.
Monotherapy has been proven insufficient in achieving sustained control of chronic hepatitis B. We aimed to assess the efficacy of combined sequential administration of lamivudine and pegylated interferon alfa-2b in patients with hepatitis Be antigen (HBeAg)-negative chronic hepatitis B.
Eighteen patients were given sequential combination treatment starting with 3 months of lamivudine monotherapy followed by 9 months of pegylated interferon alfa-2b (after a 3-month period of concomitant administration of the two drugs) and 24 patients received lamivudine monotherapy.
At the end of treatment, 88.9% of the patients who received sequential combination treatment and 70.8% of those who received lamivudine monotherapy had hepatitis B virus (HBV) DNA levels below 400 copies/mL (P = not significant). At the end of treatment, 72.2% of the patients who received sequential combination treatment and 70.8% of those who received lamivudine monotherapy achieved alanine aminotransferase normalization (P = not significant). After 12 months of follow up, 33.3% of the patients who received sequential combination treatment and 16.7% of those who received lamivudine monotherapy had HBV-DNA levels below 400 copies/mL (P = 0.4). After 12 months of follow up, 72.2% of the patients who received sequential combination treatment and 25.0% of those who received lamivudine monotherapy had normal alanine aminotransferase levels (P < 0.01). Twenty-five percent of the patients in the lamivudine monotherapy group had virological breakthrough compared to none in the sequential combination treatment group (P = 0.06).
Sequential combination treatment is able to improve sustained biochemical response rates and prevent the emergence of lamivudine-resistant mutants in patients with HBeAg-negative chronic hepatitis B.
已证实单一疗法不足以实现慢性乙型肝炎的持续控制。我们旨在评估拉米夫定与聚乙二醇化干扰素α-2b序贯联合给药对乙型肝炎e抗原(HBeAg)阴性慢性乙型肝炎患者的疗效。
18例患者接受序贯联合治疗,先进行3个月的拉米夫定单药治疗,随后进行9个月的聚乙二醇化干扰素α-2b治疗(在两种药物联合给药3个月后),24例患者接受拉米夫定单药治疗。
治疗结束时,接受序贯联合治疗的患者中88.9%以及接受拉米夫定单药治疗的患者中70.8%的乙型肝炎病毒(HBV)DNA水平低于400拷贝/毫升(P = 无显著性差异)。治疗结束时,接受序贯联合治疗的患者中72.2%以及接受拉米夫定单药治疗的患者中70.8%实现了丙氨酸转氨酶正常化(P = 无显著性差异)。随访12个月后,接受序贯联合治疗的患者中33.3%以及接受拉米夫定单药治疗的患者中16.7%的HBV-DNA水平低于400拷贝/毫升(P = 0.4)。随访12个月后,接受序贯联合治疗的患者中72.2%以及接受拉米夫定单药治疗的患者中25.0%的丙氨酸转氨酶水平正常(P < 0.01)。拉米夫定单药治疗组25%的患者出现病毒学突破,而序贯联合治疗组无患者出现(P = 0.06)。
序贯联合治疗能够提高HBeAg阴性慢性乙型肝炎患者的持续生化应答率,并预防拉米夫定耐药突变体的出现。