首页> 外文期刊>Journal of viral hepatitis. >Higher doses of peginterferon alpha-2b administered twice weekly improve sustained virological response in difficult-to-treat patients with chronic hepatitis C: results of a pilot randomized study.
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Higher doses of peginterferon alpha-2b administered twice weekly improve sustained virological response in difficult-to-treat patients with chronic hepatitis C: results of a pilot randomized study.

机译:每周两次高剂量的聚乙二醇干扰素α-2b可以改善难以治疗的慢性丙型肝炎患者的持续病毒学应答:一项随机试验的结果。

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SUMMARY: Beside substantial progress in treatment of chronic hepatitis C (CHC) particular patients (genotype 1/4, high viral load, previous nonresponse, cirrhosis) remain difficult to treat. The aim of our pilot randomized study was to compare efficacy and tolerability of standard doses of Peginterferon alpha-2b + ribavirin with higher doses of Peginterferon alpha-2b administered twice weekly + ribavirin. Sixty-five outpatients with CHC were subsequently enrolled. Group A (n = 22) received recommended doses of Peginterferon alpha-2b and group B (n = 43), received high doses twice weekly. Groups were comparable for baseline characteristics. All genotype 1/4 patients had high baseline viraemia. Sustained virological response (SVR) was significantly higher in group B among naive patients (72%vs 25%, P = 0.024). A significantly higher rate of SVR was observed in group B both considering only genotype 1/4 patients, (46%vs 13%, P = 0.03) and grouping together genotype 1/4 naive and relapsers (57%vs 11%, P = 0.039). Discontinuation rate was 32% (7 of 22) in group A and 21% (9 [corrected] of 43) in group B. Our response rates are the highest reported for genotype 1/4 with high viraemia. Our pilot study supports the need of randomized studies to evaluate both viral kinetics and efficacy of high dose and twice weekly administration of Peginterferon alpha-2b in genotype 1/4 patients with high viraemia who may need personalized treatment schedules.
机译:摘要:除了在治疗慢性丙型肝炎(CHC)方面取得实质性进展外,特定患者(基因型1/4,高病毒载量,先前无反应,肝硬化)仍然难以治疗。我们的先导随机研究的目的是比较标准剂量的Peginterferonα-2b+利巴韦林与较高剂量的Peginterferonα-2b每周两次+利巴韦林的疗效和耐受性。随后招募了65名CHC门诊患者。 A组(n = 22)接受推荐剂量的Peginterferon alpha-2b,B组(n = 43)接受高剂量,每周两次。各组的基线特征具有可比性。所有基因型1/4的患者都有较高的基线病毒血症。 B组在未接受过治疗的患者中,持续病毒学应答(SVR)显着更高(72%vs 25%,P = 0.024)。仅考虑基因型1/4的患者(46%vs 13%,P = 0.03)以及将基因型1/4初次和复发型患者分组(57%vs 11%,P = 2),在B组中观察到SVR的比率明显升高。 0.039)。 A组的停药率为32%(22个中的7个),B组的停药率为21%(43个中的9个[更正])。我们的反应率是报道的高病毒血症基因型1/4的最高。我们的先导研究支持需要进行随机研究来评估高剂量病毒动力学和功效,以及每周两次两次对Peginterferonα-2b的基因型1/4高病毒血症患者进行治疗,这些患者可能需要个性化的治疗方案。

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