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聚乙二醇干扰素联合利巴韦林治疗既往部分应答者。

Consensus interferon used to treat prior partial-responders to pegylated interferon plus ribavirin.

机构信息

Rush University Medical Center, Chicago, IL, USA.

出版信息

Dig Dis Sci. 2011 Oct;56(10):3032-7. doi: 10.1007/s10620-011-1869-6. Epub 2011 Aug 31.

DOI:10.1007/s10620-011-1869-6
PMID:21879283
Abstract

BACKGROUND

The response to pegylated interferon (peg-IFN) plus ribavirin therapy remains less than ideal with 40-50% of treated subjects failing to clear the virus. Moreover, retreatment is only minimally effective. Consensus interferon (c-IFN) has been shown to be efficacious in HCV genotype 1 patients who have failed therapy with peg-IFN.

AIM

To evaluated the response to re-treatment of peg-IFN plus ribavirin partial-responders with c-IFN plus ribavirin.

METHODS

Forty-two subjects who had previously failed to clear virus after treatment with peg-IFN plus ribavirin were treated with c-IFN (15 μg/day) plus ribavirin (800-1,200 mg/day) until 12 months of therapy or a total of six consecutive months of PCR negativity was achieved.

RESULTS

The study population consisted predominantly of males (71%), Caucasians (76%), with African Americans comprising the remaining 24%, subjects with HCV genotype 1 infection (81%) and 21% had cirrhosis by liver biopsy. The overall SVR rate was 29%. The only pretreatment variable that distinguished responders from partial-responders was the serum triglyceride level.

CONCLUSIONS

The use of c-IFN plus ribavirin in the retreatment of prior peg-IFN plus ribavirin partial responders is essentially twice that achieved in prior re-treatment regimens consisting of a second course of peg-IFN plus ribavirin. These results will need to be evaluated against the use of triple therapy consisting of a peg-IFN plus ribavirin and a protease inhibitor. More studies utilizing c-IFN plus ribavirin with either a protease inhibitor or polymerase inhibitor need to be performed as well.

摘要

背景

聚乙二醇干扰素(peg-IFN)加利巴韦林治疗的反应仍不理想,40-50%的治疗对象未能清除病毒。此外,再治疗的效果也微乎其微。共识干扰素(c-IFN)已被证明对 peg-IFN 治疗失败的 HCV 基因型 1 患者有效。

目的

评估聚乙二醇干扰素加利巴韦林部分应答者用 c-IFN 加利巴韦林再治疗的反应。

方法

42 例先前用 peg-IFN 加利巴韦林治疗未能清除病毒的患者接受 c-IFN(15μg/天)加利巴韦林(800-1200mg/天)治疗,直至治疗 12 个月或连续 6 个月 PCR 阴性。

结果

研究人群主要由男性(71%)、白种人(76%)组成,其余 24%为非裔美国人,HCV 基因型 1 感染(81%),21%的患者经肝活检证实有肝硬化。总的 SVR 率为 29%。区分应答者和部分应答者的唯一预处理变量是血清甘油三酯水平。

结论

在 peg-IFN 加利巴韦林治疗的先前部分应答者的再治疗中使用 c-IFN 加利巴韦林,基本上是先前再治疗方案(第二次 peg-IFN 加利巴韦林疗程)的两倍。这些结果需要与包含 peg-IFN 加利巴韦林和蛋白酶抑制剂的三联治疗进行比较。还需要进行更多使用 c-IFN 加利巴韦林与蛋白酶抑制剂或聚合酶抑制剂的研究。

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本文引用的文献

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Boceprevir for previously treated chronic HCV genotype 1 infection.博赛泼维用于治疗既往慢性 HCV 基因 1 型感染。
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Boceprevir for untreated chronic HCV genotype 1 infection.博赛泼维用于治疗未经治疗的慢性 HCV 基因 1 型感染。
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Ribavirin concentration in the later stages of 48 week pegylated interferon-alpha2b plus ribavirin therapy for chronic hepatitis C is useful for predicting virological response.聚乙二醇干扰素-α2b 联合利巴韦林治疗慢性丙型肝炎 48 周后利巴韦林浓度可用于预测病毒学应答。
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Efficacy of boceprevir, an NS3 protease inhibitor, in combination with peginterferon alfa-2b and ribavirin in treatment-naive patients with genotype 1 hepatitis C infection (SPRINT-1): an open-label, randomised, multicentre phase 2 trial.Boceprevir,一种 NS3 蛋白酶抑制剂,联合聚乙二醇干扰素 alfa-2b 和利巴韦林治疗初治基因 1 型丙型肝炎感染患者的疗效(SPRINT-1):一项开放标签、随机、多中心 2 期临床试验。
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