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首页> 外文期刊>JAIDS: Journal of acquired immune deficiency syndromes >Randomized trial comparing dose reduction and growth factor supplementation for management of hematological side effects in HIV/hepatitis C virus patients receiving pegylated-interferon and ribavirin.
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Randomized trial comparing dose reduction and growth factor supplementation for management of hematological side effects in HIV/hepatitis C virus patients receiving pegylated-interferon and ribavirin.

机译:比较减少剂量和生长因子补充剂治疗接受聚乙二醇干扰素和利巴韦林的HIV /丙型肝炎病毒患者血液学副作用的随机试验。

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摘要

BACKGROUND: Pegylated-interferon (PEG-IFN) and ribavirin (RBV), current standard treatment for hepatitis C virus (HCV) infection, are frequently associated with neutropenia and anemia, leading to high treatment discontinuation rates in HIV/HCV-coinfected patients. Our objective was to compare the effectiveness of intervening with hematologic growth factors versus dose reductions of standard HCV therapy for the management of treatment-induced hematologic disorders. METHODS: Ninety-two HIV/HCV-coinfected, therapy-naive subjects received PEG-IFN alfa-2b 1.5 mug.kg(1).wk(1) and RBV 13 +/- 2 mg.kg(1).d(1) for up to 48 weeks. Before treatment initiation, subjects were randomized to subsequently receive growth factors, recombinant human erythropoietin (rHuEPO) and/or granulocyte colony-stimulating factor, or dose reduction (RBV and/or PEG-IFN) for anemia and neutropenia management, respectively. We analyzed the ability of each management strategy to control anemia and neutropenia and the percentage of subjects who achieved a successful treatment outcome according to the different management strategies. RESULTS: During treatment, 43 subjects developed anemia (human erythropoietin, n = 24; dose reduction, n = 19), whereas 25 subjects developed neutropenia (granulocyte colony-stimulating factor, n = 10; dose reduction, n = 15). After the intervention, the increase in both hemoglobin and absolute neutrophil counts did not differ between the 2 side effect management strategies. Sustained response percentages were similar comparing anemic and neutropenic subjects regardless of management strategy (anemia: recombinant human erythropoietin, 29% versus dose reduction, 21%, P = 0.92; neutropenia: granulocyte colony-stimulating factor, 40% versus dose reduction, 20%, P = 0.46). CONCLUSIONS: Growth factor supplementation and dose reduction do not seem to differ as management strategies for anemia and neutropenia in HIV/HCV-coinfected individuals treated with PEG-IFN/RBV.
机译:背景:聚乙二醇干扰素(PEG-IFN)和利巴韦林(RBV)是目前丙型肝炎病毒(HCV)感染的标准治疗方法,经常与中性粒细胞减少和贫血相关,导致HIV / HCV合并感染患者的治疗中断率很高。我们的目标是比较介入血液生长因子干预与标准HCV治疗的剂量减少对治疗性血液疾病管理的有效性。方法:接受过HIV / HCV感染的92名未接受治疗的受试者接受了PEG-IFN alfa-2b 1.5 mug.kg(1).wk(1)和RBV 13 +/- 2 mg.kg(1).d( 1)长达48周。在开始治疗之前,将受试者随机分为两组,分别接受生长因子,重组人促红细胞生成素(rHuEPO)和/或粒细胞集落刺激因子,或减少剂量(RBV和/或PEG-IFN)治疗贫血和中性粒细胞减少。我们分析了每种管理策略控制贫血和中性粒细胞减少的能力以及根据不同管理策略获得成功治疗结果的受试者的百分比。结果:在治疗过程中,有43名受试者出现贫血(人类促红细胞生成素,n = 24;剂量减少,n = 19),而25名受试者出现中性白细胞减少(粒细胞集落刺激因子,n = 10;剂量减少,n = 15)。干预后,两种副作用管理策略之间血红蛋白和绝对中性粒细胞计数的增加没有差异。无论采用何种管理策略,贫血和中性粒细胞减少受试者的持续缓解率相似(贫血:重组人促红细胞生成素,减少剂量占29%,21%,P = 0.92;中性粒细胞减少:粒细胞集落刺激因子,减少剂量,占40%,20% ,P = 0.46)。结论:生长因子补充和剂量减少似乎没有差异,因为在接受PEG-IFN / RBV治疗的HIV / HCV合并感染的个体中,贫血和中性粒细胞减少的管理策略。

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