Johnson K, Green P K, Ioannou G N
Division of General Internal Medicine, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA, USA.
Division of Research and Development, Veterans Affairs Puget Sound Healthcare System, Seattle, WA, USA.
J Viral Hepat. 2017 Nov;24(11):966-975. doi: 10.1111/jvh.12731. Epub 2017 Jul 12.
We aimed to determine whether the HCV viral load after four weeks of treatment (W4VL) with direct-acting antiviral agents (DAAs) predicts sustained virologic response (SVR) in a real-world clinical setting. We identified 21 095 patients who initiated DAA-based antiviral treatment in the national Veterans Affairs (VA) healthcare system from 01/01/2014 to 06/30/2015. Week 4 viral load was categorized as undetectable, detectable below quantification (DBQ), detectable above quantification (DAQ) with viral load ≤42 IU/mL and DAQ with viral load >42 IU/mL. Week 4 viral load was undetectable in 36.1%, detectable below quantification in 45.6%, DAQ ≤42 in 9.3%, DAQ >42 in 9.1%. Detectable above quantification was much more common and undetectable week 4 viral load much less common when tested with the Abbott RealTime HCV assay vs the Roche COBAS AmpliPrep/COBAS TaqMan Version 2 assay. Compared to patients with undetectable week 4 viral load (SVR=93.5%), those with detectable below quantification (SVR=91.8%, adjusted odds ratio [AOR] 0.79, P-value=.001), DAQ ≤42 (SVR=90.0%, AOR 0.63, P-value<.001) and DAQ >42 (SVR=86.2%, AOR 0.52, P-value<.001) had progressively lower likelihood of achieving SVR after adjusting for baseline characteristics and treatment duration. Among genotype 1-infected patients who were potentially eligible for 8-week sofosbuvir/ledipasvir monotherapy, we did not find evidence that treatment for 12 weeks instead of 8 weeks was associated with higher SVR, even among those with detectable above quantification. In summary, DBQ and DAQ W4VL are very common in real-world practice, contrary to what was reported in clinical trials, and strongly predict reduced SVR across genotypes and clinically relevant patient subgroups. Whether and how week 4 viral load results should influence treatment decisions requires further study.
我们旨在确定在真实临床环境中,使用直接作用抗病毒药物(DAA)治疗四周后的丙型肝炎病毒载量(W4VL)是否能预测持续病毒学应答(SVR)。我们在国家退伍军人事务部(VA)医疗系统中,识别出2014年1月1日至2015年6月30日期间开始接受基于DAA的抗病毒治疗的21095名患者。第4周病毒载量被分类为不可检测、低于定量下限可检测(DBQ)、病毒载量≤42 IU/mL时高于定量下限可检测(DAQ)以及病毒载量>42 IU/mL时高于定量下限可检测(DAQ)。第4周病毒载量不可检测的占36.1%,低于定量下限可检测的占45.6%,DAQ≤42的占9.3%,DAQ>42的占9.1%。与使用罗氏COBAS AmpliPrep/COBAS TaqMan 2.0版检测相比,使用雅培实时丙型肝炎病毒检测时,高于定量下限可检测更为常见,而第4周病毒载量不可检测则更为少见。与第4周病毒载量不可检测的患者(SVR = 93.5%)相比,低于定量下限可检测的患者(SVR = 91.8%,调整后比值比[AOR] 0.79,P值 = 0.001)、DAQ≤42的患者(SVR = 90.0%,AOR 0.63,P值<0.001)以及DAQ>42的患者(SVR = 86.2%,AOR 0.52,P值<0.001)在调整基线特征和治疗时长后,实现SVR的可能性逐渐降低。在可能符合8周索磷布韦/维帕他韦单药治疗条件的基因1型感染患者中,我们未发现证据表明12周而非8周的治疗与更高的SVR相关,即使在高于定量下限可检测的患者中也是如此。总之,在真实临床实践中,DBQ和DAQ W4VL非常常见,这与临床试验中的报告情况相反,并且强烈预示着各基因型和临床相关患者亚组的SVR降低。第4周病毒载量结果是否以及如何影响治疗决策需要进一步研究。