Mellerup M T, Krogsgaard K, Mathurin P, Gluud C, Poynard T
The Copenhagen Trial Unit, Copenhagen University Hospital, H:S Rigshospitalet, Blegdamsvej 9, Copenhagen, Denmark, DK-2100.
Cochrane Database Syst Rev. 2002(2):CD000345. doi: 10.1002/14651858.CD000345.
Chronic hepatitis B has serious effects on morbidity and mortality. Alfa interferon has been shown to increase the rates of HBeAg-clearance as well as seroconversion to anti-HBe, but response rates are unsatisfactory. Glucocorticosteroid pretreatment may increase the response to alfa interferon.
The objectives were to assess the effects of the sequential combination of glucocorticosteroids and alfa interferon versus alfa interferon alone in hepatitis B 'e' antigen positive chronic hepatitis B on mortality, virological response, biochemical response, liver histology, quality of life, and adverse events.
Electronic searches of the controlled trial registers of The Cochrane Hepato-Biliary Group and The Cochrane Library, MEDLINE, BIOSIS, and EMBASE were combined (May 2000). Reading the bibliography of retrieved articles identified further trials. Alfa interferon-manufacturing companies were approached in order to inquire about any published and unpublished randomised trials.
The analyses included randomised trials comparing identical alfa interferon treatment regimens with and without glucocorticosteroid pretreatment for hepatitis B 'e' antigen positive chronic hepatitis. The trials could be open, single blinded, or double blinded. No patient exclusion criteria were applied.
Three reviewers independently selected the trials and one extracted the data, which were validated. Assessments of the outcome measures were performed at the end of treatment and at six months and at maximal follow up after the end of treatment with alfa interferon.
A total of 13 randomised trials including 790 patients were included. Loss of hepatitis B 'e' antigen (OR 1.41, 95% confidence interval 1.03 to 1.92, P = 0.03) and hepatitis B virus DNA (OR = 1.51, 95% confidence interval 1.12 to 2.05, P = 0.008) were significantly more frequent among patients treated with the sequential combination of glucocorticosteroids and alfa interferon than among patients treated with alfa interferon alone. Glucocorticosteroid pretreatment did not significantly influence seroconversion from hepatitis B 'e' antigen to antibodies to hepatitis B 'e' antigen, loss of hepatitis B surface antigen, normalisation of alanine aminotransferase/aspartate aminotransferase activities, and severity of adverse events. Glucocorticosteroid pretreatment did not significantly affect mortality and adverse events. The effect of glucocorticosteroid pretreatment on liver histology and quality of life could not be assessed due to insufficient data.
REVIEWER'S CONCLUSIONS: Pretreatment with glucocorticosteroids before treatment with alfa interferon in patients with hepatitis B 'e' antigen positive chronic hepatitis B may be more effective than treatment with alfa interferon alone with regard to loss of hepatitis B 'e' antigen and hepatitis B virus DNA, but evidence for effect on clinical outcomes is lacking.
慢性乙型肝炎对发病率和死亡率有严重影响。已证实α干扰素可提高HBeAg清除率以及抗HBe血清学转换率,但应答率并不理想。糖皮质激素预处理可能会增加对α干扰素的应答。
评估糖皮质激素与α干扰素序贯联合治疗对比单独使用α干扰素治疗乙型肝炎e抗原阳性慢性乙型肝炎对死亡率、病毒学应答、生化应答、肝脏组织学、生活质量及不良事件的影响。
2000年5月,对Cochrane肝胆组和Cochrane图书馆的对照试验注册库、MEDLINE、BIOSIS及EMBASE进行了电子检索,并将结果合并。通过阅读检索到文章的参考文献来确定更多试验。与α干扰素生产公司联系,询问其已发表和未发表的随机试验情况。
分析纳入了比较相同α干扰素治疗方案在有或无糖皮质激素预处理情况下治疗乙型肝炎e抗原阳性慢性乙型肝炎的随机试验。试验可以是开放、单盲或双盲的。未应用患者排除标准。
三位综述作者独立选择试验,一位提取数据并进行验证。在治疗结束时、治疗结束后6个月以及α干扰素治疗结束后的最长随访期对结局指标进行评估。
共纳入13项随机试验,涉及790例患者。糖皮质激素与α干扰素序贯联合治疗的患者中,HBeAg消失(比值比1.41,95%置信区间1.03至1.92,P = 0.03)及乙肝病毒DNA消失(比值比 = 1.51,95%置信区间1.12至2.05,P = 0.008)的情况显著多于单独使用α干扰素治疗的患者。糖皮质激素预处理对HBeAg向抗HBe血清学转换、HBsAg消失、丙氨酸氨基转移酶/天冬氨酸氨基转移酶活性恢复正常及不良事件严重程度无显著影响。糖皮质激素预处理对死亡率及不良事件无显著影响。由于数据不足,无法评估糖皮质激素预处理对肝脏组织学及生活质量的影响。
对于乙型肝炎e抗原阳性慢性乙型肝炎患者,在使用α干扰素治疗前进行糖皮质激素预处理,在HBeAg及乙肝病毒DNA消失方面可能比单独使用α干扰素治疗更有效,但缺乏对临床结局影响的证据。