首页> 美国卫生研究院文献>British Medical Journal >Randomised controlled trial of lymphoblastoid interferon alfa in Europid men with chronic hepatitis B virus infection.
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Randomised controlled trial of lymphoblastoid interferon alfa in Europid men with chronic hepatitis B virus infection.

机译:在欧洲慢性乙型肝炎病毒感染男性中淋巴母细胞干扰素α的随机对照试验。

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摘要

OBJECTIVE--To confirm the findings of pilot studies that interferon alfa is an effective treatment of Europid men with chronic hepatitis B virus infection. DESIGN--Randomised controlled trial of three months treatment with interferon alfa followed by 12 months of observation. SETTING--Outpatient clinic of a tertiary referral centre. PATIENTS--37 Treated men (six anti-HIV positive) and 34 untreated men (nine anti-HIV positive) who met the criteria for the trial. Four controls failed to complete follow up. INTERVENTIONS--The treated group received subcutaneous injections of 5-10 MU interferon alfa/m2 daily for five days, then 10 MU/m2 thrice weekly for 11 weeks. Follow up continued at monthly intervals for 12 months. Untreated controls were monitored over the same period. MAIN OUTCOME MEASURE--Hepatitis B e antigen and hepatitis B virus DNA state after 15 months of observation. RESULTS--12 Of the 37 treated patients cleared hepatitis B e antigen and hepatitis B virus DNA, whereas only one of 30 untreated controls seroconverted over the same period--an increased response rate of 29% (95% confidence interval 13% to 45%). The life table estimate of response at 15 months was 35% in treated patients, an increase of 32% above controls (95% confidence interval 16% to 48%). The response rates in groups by predictive pretreatment variables were 12 of 31 anti-HIV negative patients (excess response 34%; 95% confidence interval 14% to 54%), 12 of 26 with chronic active hepatitis before treatment (excess response 46%; 27% to 65%), and 12 of 21 with a pretreatment serum aspartate aminotransferase activity greater than 70 IU/l (excess response 46%; 16% to 76%). The combination of these factors predicted response with a sensitivity of 100% and a specificity of 80%. Four of the 12 responders, who had all been infected for less than two years, also lost hepatitis B surface antigen. Treatment was well tolerated. CONCLUSIONS--Interferon alfa is effective in the treatment of a proportion of Europid men with chronic hepatitis B virus infection, who might be identified before treatment. Additional strategies are required to improve the rate of response.
机译:目的-为了证实先驱性研究的结果,即干扰素α是对欧洲慢性乙型肝炎病毒感染男性的有效治疗。设计-随机对照试验,进行了三个月的干扰素α治疗,观察了12个月。地点-三级转诊中心的门诊诊所。患者-符合试验标准的37名接受治疗的男性(6名抗HIV阳性)和34名未经治疗的男性(9名抗HIV阳性)。四个控制措施未能完成跟进。干预措施-治疗组每天皮下注射5-10 MU / m2干扰素α/ m2,持续5天,然后每周三次10 MU / m2,持续11周。每月持续随访12个月。同期监测未处理的对照。主要观察指标-观察15个月后,乙型肝炎e抗原和乙型肝炎病毒DNA状况。结果--12在接受治疗的37名患者中,清除了乙型肝炎e抗原和乙型肝炎病毒DNA,而同期未进行血清治疗的30名未接受治疗的对照组中只有一名进行了血清转化-应答率提高了29%(95%的置信区间为13%至45 %)。根据生命表,接受治疗的患者在15个月时的反应估计为35%,比对照组增加了32%(95%置信区间为16%至48%)。根据预测的治疗前变量,各组的缓解率分别为31例抗HIV阴性患者中的12例(过度缓解34%; 95%置信区间14%至54%),26例慢性活动性肝炎患者中的12例(过度缓解46%; 27%至65%),以及21例中有12例的预处理血清天冬氨酸转氨酶活性大于70 IU / l(反应过度46%; 16%至76%)。这些因素共同预测了响应,灵敏度为100%,特异性为80%。感染时间均不足两年的12位应答者中有4位也丢失了乙肝表面抗原。治疗耐受性良好。结论:α干扰素可有效治疗一部分欧洲慢性乙型肝炎病毒感染的男性,可在治疗前确定。需要其他策略来提高响应速度。

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