Métreau J M
Service d'Hépatologie, Hôpital Henri Mondor, Créteil, France.
Gut. 1993;34(2 Suppl):S112-3. doi: 10.1136/gut.34.2_suppl.s112.
One hundred and eleven patients with non-A, non-B/type C (NANB/C) chronic active hepatitis were randomly assigned to two groups to receive recombinant interferon alfa-2b treatment as follows: 3 million units (MU) interferon three times weekly for six months or 3 MU interferon three times weekly for the first six months, 2 MU for the next three months, and 1 MU for the last three months. At the end of treatment, the number who had responded completely was similar in both groups (47.2% in the six months group v 41.4% in the 12 months group). Cirrhosis was found to be the only predictive factor for response; a complete response was observed in 50.6% of patients without cirrhosis v 33.3% of those with cirrhosis (p = 0.04). After one year of treatment, the rate of relapse was lower in patients who had received longer treatment (33%) than in those who had received six months of interferon (60%). The difference between the groups was not statistically significant and the trend favouring longer treatment for sustained response requires further confirmation.
111例非甲非乙/丙型(NANB/C)慢性活动性肝炎患者被随机分为两组,接受如下重组干扰素α-2b治疗:一组为300万单位(MU)干扰素,每周3次,共6个月;另一组为前6个月3MU干扰素每周3次,接下来3个月2MU,最后3个月1MU。治疗结束时,两组完全缓解的人数相似(6个月组为47.2%,12个月组为41.4%)。发现肝硬化是唯一的反应预测因素;无肝硬化患者的完全缓解率为50.6%,而有肝硬化患者为33.3%(p=0.04)。治疗1年后,接受更长疗程治疗的患者复发率(33%)低于接受6个月干扰素治疗的患者(60%)。两组之间的差异无统计学意义,支持更长疗程治疗以获得持续缓解的趋势需要进一步证实。