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首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Response-guided therapy for patients with chronic hepatitis who have high viral loads of hepatitis C virus genotype 2
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Response-guided therapy for patients with chronic hepatitis who have high viral loads of hepatitis C virus genotype 2

机译:应对指导疗法用于病毒载量为C型肝炎2型病毒的慢性肝炎患者

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Aim: We evaluated the efficacy of response-guided therapy in patients with hepatitis C virus (HCV) genotype 2. Methods: We studied 105 patients with an HCV genotype 2 load of higher than 5.0Log IU/mL who received more than 75% of the target dose of pegylated interferon plus ribavirin. Among patients with rapid viral response (RVR; no HCV RNA detected at week 4), 14 selected 16weeks of therapy (group A), and 28 selected 24weeks of therapy (group B). Among non-RVR patients, 40 selected 24weeks of therapy (group C), and 19 selected 48weeks of therapy (group D). Results: All patients in group A and B achieved a sustained viral response (SVR). Clinical characteristics did not differ significantly between groups C and D. However, the proportion of patients in whom HCV RNA disappeared at a later week after starting treatment was higher in group D (P=0.0578). SVR rate was 73% in C, and 79% in D. Among patients in whom HCV RNA disappeared between weeks 5 and 8, SVR was achieved in 28 (82%) of 34 patients in C and 10 (91%) of 11 patients in D. Among patients whose HCV RNA disappeared between weeks 9 and 12, SVR was achieved in one (20%) of five patients in C and five (63%) of eight patients in D (not statistically significant). Conclusions: 16weeks of combination therapy could achieve an adequate antiviral effect for RVR patients. Extending therapy could not significantly improve SVR rate in non-RVR patients.
机译:目的:我们评估了应答指导疗法对丙型肝炎病毒(HCV)基因型2患者的疗效。方法:我们研究了105例HCV基因型2负荷高于5.0Log IU / mL的患者,他们接受了超过75%的聚乙二醇干扰素加利巴韦林的目标剂量。在具有快速病毒反应(RVR;在第4周未检测到HCV RNA)的患者中,有14个选择的治疗16周(A组)和28个选择的治疗24周(B组)。在非RVR患者中,有40名选择了24周治疗(C组),有19名选择了48周治疗(D组)。结果:A组和B组的所有患者均实现了持续病毒应答(SVR)。 C组和D组之间的临床特征无明显差异。但是,D组开始治疗后的HCV RNA消失的患者比例更高(P = 0.0578)。 C的SVR率为73%,D的SVR率为79%。在5至8周内HCV RNA消失的患者中,C的34例患者中28例(82%)和11例中的10例(91%)达到了SVR。在第9周到第12周之间HCV RNA消失的患者中,C组5例患者中的1名(20%)和D组8例患者中的5名(63%)实现了SVR(无统计学意义)。结论:16周联合治疗对RVR患者可取得足够的抗病毒作用。在非RVR患者中,扩大治疗不能显着提高SVR率。

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