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Closing in on the target: Sustained virologic response in hepatitis C virus genotype 1 infection response-guided therapy

机译:达成目标:丙型肝炎病毒基因型1感染应答指导治疗中持续的病毒学应答

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摘要

Retrospective analyses of the boceprevir and telaprevir phase 3 trial data demonstrate the clinical relevance of detected but not quantifiable hepatitis C virus (HCV) genotype 1 RNA during treatment. These analyses illustrate the importance of using precise and standard terminology in reporting low-level HCV RNA results for consistent data collection across clinical trials, and to ensure optimal virologic response-guided treatment decision making in clinical practice. In the context of currently available quantitative HCV RNA assays, we clarify that unquantifiable HCV RNA should be classified as target detected or target not detected, as both have been shown to reflect clinically different qualitative HCV RNA levels during treatment. Additionally, use of terms such as "undetectable" or "below limit of detection" should be avoided as such terms are imprecise, not consistently defined, and often misinterpreted.
机译:对boceprevir和telaprevir 3期试验数据的回顾性分析表明,在治疗过程中检测到但无法量化的丙型肝炎病毒(HCV)基因型1 RNA具有临床相关性。这些分析说明了使用精确和标准的术语报告低水平HCV RNA结果对于整个临床试验中一致的数据收集以及确保在临床实践中以最佳的病毒学应答为指导的治疗决策的重要性。在目前可用的定量HCV RNA测定方法的背景下,我们澄清了不可量化的HCV RNA应归类为检测到的靶标或未检测到的靶标,因为这两种化合物均已显示出在治疗过程中反映出临床上不同的定性HCV RNA水平。另外,应避免使用诸如“不可检测的”或“检测极限以下”之类的术语,因为此类术语不精确,定义不一致,经常被误解。

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