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Low daily dosage of interferon for 1 year after HCV-related end-therapy response. A randomized-controlled study.

机译:与HCV相关的最终治疗反应后1年中每天低剂量的干扰素。一项随机对照研究。

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摘要

This randomized controlled study involved 236 1b genotype (121 males) naive patients with chronic hepatitis C. After a course of interferon (IFN)-alpha2b plus ribavirin for 6 or 12 months, 117 (49.5%) of the end-therapy responders were equally divided into two groups and were assigned to receive either low daily doses of IFN-alpha2b (1.5 MU) 'consolidation therapy' (59 patients) for 1 year or no further treatment (58 patients). At the end of the follow-up period (6 months), the number of sustained responders in the consolidation group (83%) was significantly higher than in the control group (37.9%). The predicting factors of both end-therapy response and sustained response were the classic ones and a lower GGT/ALT ratio (GGT: gamma-glutamyl transpeptidase; ALT: alanine aminotransferase). The strongest predictors of sustained response alone were consolidation therapy and the longer period on combined treatment (12 vs 6 months). Consolidation therapy was better tolerated than the previously prescribed combined therapy in terms of side effects. In conclusion, genotype 1b naive end-therapy responders to usual combined therapy, after a period of daily consolidation therapy with a low dosage of IFN without ribavirin, achieved a better rate of sustained response than the control group.
机译:这项随机对照研究涉及236位1b基因型(121位男性)未治疗的慢性丙型肝炎患者。在干扰素(IFN)-α2b加利巴韦林治疗6或12个月后,有117(49.5%)名患者接受了最终治疗分为两组,分别接受每日低剂量的IFN-α2b(1.5 MU)'巩固治疗'(59例)一年或不接受进一步治疗(58例)。在随访期(6个月)结束时,巩固组的持续缓解人数(83%)显着高于对照组(37.9%)。最终治疗反应和持续反应的预测因素是经典因素和较低的GGT / ALT比(GGT:γ-谷氨酰转肽酶; ALT:丙氨酸转氨酶)。持续治疗的最强预测因素是巩固治疗和联合治疗的时间更长(12 vs 6个月)。就副作用而言,合并治疗比先前规定的联合治疗耐受性更好。综上所述,基因型1b初次接受终末治疗的患者对常规联合治疗的反应是,在每天进行低剂量无利巴韦林干扰素的巩固治疗后,与对照组相比,获得了更好的持续应答率。

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