Cagnoni C, Pancotti D, Carrara G
2nd Dept. of Medicine, Civil Hospital, Piacenza, Italy.
Hepatogastroenterology. 2000 Jan-Feb;47(31):199-203.
BACKGROUND/AIMS: To evaluate leukocyte interferon-alpha tolerability and efficacy in the retreatment of patients poorly tolerant to recombinant interferon-alpha.
Patients with chronic hepatitis C, poorly tolerant to a previous interferon-alpha treatment (118 patients; 73 "relapsers": Group I; 45 "non-responders": Group II) were retreated with 6 MU tiw of leukocyte interferon-alpha for 6 months and then followed-up for 12-34 months. Only patients with complete regression of any previous interferon-related adverse event were included.
Three patients dropped out due to recurrence of a severe depressive syndrome. In 86/115 patients (75%) no significant lifestyle changes versus baseline were observed during retreatment, while 29 subjects experienced a moderately negative interference on their living habits. The different influence on the patients' quality of life of leukocyte interferon in comparison with the previous treatment was significant (P < 0.001). In 98 patients the interferon-related adverse events significantly decreased. After 12 months of follow-up, a sustained biochemical response was observed in 40 patients (Group I:31; Group II:9), and a persistent virological response in 28 (Group I:23; Group II:5).
The good compliance with leukocyte interferon administration shown by poorly tolerant patients, non-responders/relapsers to recombinant interferon, permitted a retreatment with full doses, so increasing the chance to obtain a larger number of sustained responses.
背景/目的:评估白细胞干扰素α对重组干扰素α耐受性差的患者再治疗时的耐受性和疗效。
对先前干扰素α治疗耐受性差的慢性丙型肝炎患者(118例;73例“复发者”:第一组;45例“无反应者”:第二组)用白细胞干扰素α 6 MU,每周3次,治疗6个月,然后随访12 - 34个月。仅纳入先前任何与干扰素相关的不良事件完全消退的患者。
3例患者因严重抑郁综合征复发而退出。在115例患者中的86例(75%)再治疗期间与基线相比未观察到明显的生活方式改变,而29例患者的生活习惯受到中度负面影响。与先前治疗相比,白细胞干扰素对患者生活质量的不同影响具有显著性(P < 0.001)。98例患者中与干扰素相关的不良事件显著减少。随访12个月后,40例患者(第一组:31例;第二组:9例)观察到持续生化反应,28例患者(第一组:23例;第二组:5例)观察到持续病毒学反应。
对重组干扰素无反应/复发且耐受性差的患者对白细胞干扰素给药的良好依从性,允许全剂量再治疗,从而增加获得更多持续反应的机会。