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First prospective comparison of genotypic vs phenotypic tropism assays in predicting virologic responses to Maraviroc (MVC) in a phase 3 study: MODERN

机译:在第3阶段研究中,基因型和表型向性分析法在预测对Maraviroc(MVC)的病毒学应答中的首次前瞻性比较:现代

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IntroductionMODERN (A4001095) was the first prospective phase 3 study comparing genotype vs phenotype (Trofile?) tropism assessments.Materials and MethodsTreatment-na?ve adults with HIV-1 RNA >1000 copies/mL were randomized 1:1 at screening to either genotype or Trofile for tropism assessment. Genotype was determined using the geno2pheno algorithm to assess triplicate HIV-1 gp120 V3 loop sequences (plasma); false-positive rate=10%. R5-virus-infected subjects were then randomized 1:1 to receive Maraviroc (MVC) 150 mg QD or Truvada 200/300 mg QD each with DRV/r 800/100 mg QD. Tropism of screening samples from enrolled subjects was also retrospectively determined using the alternate testing method. Positive predictive values (PPV) were estimated by%R5 subjects with Week 48 HIV-1 RNA < 50 c/mL. PPV for each assay was estimated using the response rate among those randomized to that assay and using model-based response estimates in those with R5 by that assay (at screening or retest).ResultsThe observed response rate was 146/181 (80.7%) for genotype vs 160/215 (74.4%) for Trofile (stratification adjusted difference=6.9%, 95% CI 1.3% to 15%). The model-based estimates of PPV (±SE) were 79.1% (±2.42) and 76.3% (±2.38), respectively (difference = 2.8%, 95% CI ?2.1% to 7.2%). There was no difference in response rate between assays in the Truvada arm (observed difference=? 0.1%, 95% CI ?6.8% to 6.6%). Most enrolled subjects had R5 results at screening using both assays (285/396 (72%)), and of these subjects, 79.3% (226/285) had HIV-1 RNA <50 c/mL at week 48 (Table 1). The few subjects classified as non-R5 by the alternate assay had similar virologic responses to the concordant R5 group.Table 1MVC week 48 response (HIV-1 RNA<50c/mL), n/N (%)
机译:简介MODERN(A4001095)是第一个比较基因型和表型(Trofile?)趋向性评估的前瞻性3期研究。材料和方法治疗初治的HIV-1 RNA> 1000拷贝/ mL的成年人在筛查任一基因型时按1:1随机分配。或Trofile进行向性评估。使用geno2pheno算法确定基因型,以评估一式三份的HIV-1 gp120 V3环序列(血浆);假阳性率= 10%。然后将R5病毒感染的受试者按1:1随机分配,以分别接受Maraviroc(MVC)150 mg QD或Truvada 200/300 mg QD,每人分别接受DRV / r 800/100 mg QD。还使用替代测试方法回顾性确定了来自入选受试者的筛查样品的取向。阳性预测值(PPV)由第48周HIV-1 RNA <50 c / mL的%R5受试者估计。使用随机化分析的应答率和通过该分析(筛选或复检)对R5进​​行评估的模型响应估计值来评估每种分析的PPV。结果观察到的PPV值为146/181(80.7%)基因型vs Trofile的160/215(74.4%)(分层调整差异= 6.9%,95%CI 1.3%至15%)。基于模型的PPV(±SE)估计分别为79.1%(±2.42)和76.3%(±2.38)(差异= 2.8%,95%CI≤2.1%至7.2%)。 Truvada组中各试验之间的反应率没有差异(观察到的差异=?0.1%,95%CI?6.8%至6.6%)。大多数入选的受试者在使用两种测定进行筛查时均具有R5结果(285/396(72%)),其中这些受试者中,在第48周时79.3%(226/285)的HIV-1 RNA <50 c / mL(表1) 。少数通过替代试验被分类为非R5的受试者与一致的R5组具有相似的病毒学应答。表1 MVC第48周应答(HIV-1 RNA <50c / mL),n / N(%)

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