Tinè F, Magrin S, Craxì A, Pagliaro L
Clinica Medica R of University of Palermo, Italy.
J Hepatol. 1991 Sep;13(2):192-9. doi: 10.1016/0168-8278(91)90814-r.
We reviewed randomised clinical trials evaluating the effect of lymphoblastoid or recombinant alpha-interferon in non-A, non-B chronic hepatitis. The outcomes assessed were the rates of serum alanine aminotransferase normalization and relapse during and after stopping interferon. Data were pooled by meta-analysis and a 50% overall rate difference, favouring treated patients, was found. Results showed homogeneity in direction of treatment effect both after short-term (2-6 months, greater than or equal to 2 mega-units thrice weekly) and long-term (9-18 months, variable dose) interferon course. Moreover, results did not change when type of publication (abstracts vs. full reports) and treatment duration or schedule were accounted for. About 50% of patients originally responding to treatment relapsed within 6 months of either dose reduction or stopping interferon, thus suggesting that only in about one out of four patients is benefit from treatment sustained up to 1 year. We conclude that larger trials are needed to identify an optimal schedule of treatment and to evaluate predictors of interferon effectiveness in patients with non-A, non-B chronic hepatitis.
我们回顾了评估淋巴母细胞样干扰素或重组α干扰素对非甲非乙型慢性肝炎疗效的随机临床试验。评估的结果是血清丙氨酸转氨酶正常化率以及在干扰素治疗期间和停药后的复发率。通过荟萃分析汇总数据,发现治疗组患者总体有效率提高了50%。结果表明,短期(2 - 6个月,每周三次,每次大于或等于2百万单位)和长期(9 - 18个月,剂量可变)干扰素疗程后,治疗效果方向具有同质性。此外,当考虑出版物类型(摘要与完整报告)以及治疗持续时间或方案时,结果并未改变。约50%最初对治疗有反应的患者在减量或停用干扰素后的6个月内复发,这表明每4名患者中只有约1名患者从治疗中获得的益处可持续长达1年。我们得出结论,需要进行更大规模的试验,以确定最佳治疗方案,并评估非甲非乙型慢性肝炎患者中干扰素疗效的预测因素。