Cammà C, Bruno S, Schepis F, Lo Iacono O, Andreone P, Gramenzi A G, Mangia A, Andriulli A, Puoti M, Spadaro A, Freni M, Di Marco V, Cino L, Saracco G, Chiesa A, Crosignani A, Caporaso N, Morisco F, Rumi M G, Craxì A
Istituto Metodologie Diagnostiche Avanzate, Consiglio Nazionale delle Ricerche, and Cattedra e Unità Operativa di Gastroenterologia, University of Palermo, Palermo, Italy.
Gut. 2002 Dec;51(6):864-9. doi: 10.1136/gut.51.6.864.
Retreatment with a combination of alpha interferon (IFN) plus ribavirin of patients with chronic hepatitis C who did not respond to IFN monotherapy has not been assessed in large controlled studies.
To assess the effectiveness and tolerability of IFN/ribavirin retreatment of non-responders to IFN and to identify predictors of complete (biochemical and virological) sustained response, we performed a meta-analysis of individual data on 581 patients from 10 centres. Retreatment with various IFN schedules (mean total dose 544 mega units) and a fixed ribavirin dose (1000-1200 mg/daily depending on body weight) was given for 24-60 (mean 39.5) weeks.
Biochemical end of treatment and sustained responses were observed in 271/581 (46.6%; 95% confidence interval (CI) 42.6-50.7%) and in 109/581 (18.7%; 95% CI 15.6-22.0%) cases, respectively. Two hundred and six of 532 patients (38.7%; 95% CI 34.6-42.9%) had an end of treatment complete response to retreatment while a complete sustained response occurred in 88 of 559 (15.7%; 95% CI 12.8-18.8%). Fifty four of 581 patients (9.2%; 95% CI 7.0-11.7%) stopped retreatment due to adverse effects. By logistic regression, complete sustained response was predicted independently by age <45 years (p=0.04), by normal pretreatment gamma-glutamyltransferase levels (p=0.01), and by a second course total IFN dose of at least 432 mega units (p=0.008).
The overall low probability of effectiveness argues against indiscriminate retreatment of all IFN monotherapy non-responders with IFN/ribavirin. Patients less than 45 years old with normal gamma-glutamyltransferase levels who were retreated with high dose long course combination therapy had a complete sustained response rate of 30%.
对于未对α干扰素(IFN)单药治疗产生应答的慢性丙型肝炎患者,采用IFN联合利巴韦林进行再治疗,尚未在大型对照研究中得到评估。
为评估IFN单药治疗无应答者接受IFN/利巴韦林再治疗的有效性和耐受性,并确定完全(生化和病毒学)持续应答的预测因素,我们对来自10个中心的581例患者的个体数据进行了荟萃分析。采用各种IFN方案(平均总剂量544百万单位)和固定的利巴韦林剂量(根据体重为1000 - 1200毫克/天)进行再治疗,疗程为24 - 60周(平均39.5周)。
分别在271/581例(46.6%;95%置信区间(CI)42.6 - 50.7%)和109/581例(18.7%;95%CI 15.6 - 22.0%)患者中观察到治疗结束时的生化应答和持续应答。532例患者中有206例(38.7%;95%CI 34.6 - 42.9%)在再治疗结束时获得完全应答,而5测到559例患者中有88例(15.7%;95%CI 12.8 - 18.8%)出现完全持续应答。581例患者中有54例(9.2%;95%CI 7.0 - 11.7%)因不良反应停止再治疗。通过逻辑回归分析,年龄<45岁(p = 0.04)、治疗前γ-谷氨酰转移酶水平正常(p = 0.01)以及第二疗程IFN总剂量至少432百万单位(p = 0.008)可独立预测完全持续应答。
总体有效性概率较低,这表明不应对所有IFN单药治疗无应答者不加选择地进行IFN/利巴韦林再治疗。年龄小于45岁、γ-谷氨酰转移酶水平正常且接受高剂量长疗程联合治疗的再治疗患者,其完全持续应答率为30%。