CHIP, Department of Infectious Diseases, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Department of Infectious Diseases, Luigi Sacco University Hospital, Milan, Italy.
AIDS. 2018 Sep 10;32(14):1995-2004. doi: 10.1097/QAD.0000000000001928.
To investigate the uptake of hepatitis C virus (HCV) therapy among HIV/HCV-coinfected patients in the pan-European EuroSIDA study between 2011 and 2016.
All HCV-RNA+ patients were included. Baseline was defined as latest of anti-HCV+, January 2011 or enrolment in EuroSIDA. The incidence of starting first interferon-free direct-acting antiviral (DAA) therapy was calculated. Factors associated with starting interferon-free DAA were determined by Poisson regression.
Among 4308 HCV-RNA+ patients (1255, 970, 663, 633, 787 from South, West, North, Central East and East Europe, respectively) with 11 863 person-years of follow-up, 1113 (25.8%) started any HCV therapy. Among patients with at least F3 fibrosis, more than 50% in all regions remained untreated. The incidence (per 1000 person-years of follow-up, 95% confidence interval) of starting DAA increased from 7.8 (5.9-9.8) in 2014 to 135.2 (122.0-148.5) in 2015 and 128.9 (113.5-144.3) in 2016. The increase was highest in North and West and intermediate in South, but remained modest in Central East and Eastern Europe. After adjustment, women, individuals from Central East or East, genotype 3, antiretroviral therapy naïve and those with detectable HIV-RNA were less likely to start DAA. Older persons, those with HCV-RNA more than 500 000 IU/ml and those with more advanced liver fibrosis were more likely to start DAA.
Uptake of DAA therapy among HIV/HCV-coinfected patients increased considerably in Western Europe between 2014 and 2016, but was modest in Central East and East. In all regions more than 50% with at least F3 fibrosis remained untreated. Women were less likely to start DAA.
本研究旨在调查 2011 年至 2016 年间,在泛欧 EuroSIDA 研究中 HIV/HCV 合并感染患者中丙型肝炎病毒(HCV)治疗的接受情况。
所有 HCV-RNA+患者均被纳入研究。基线定义为抗 HCV+的最新时间点、2011 年 1 月或 EuroSIDA 入组时间。计算开始首个无干扰素直接作用抗病毒(DAA)治疗的发生率。采用泊松回归确定与开始无干扰素 DAA 治疗相关的因素。
在 4308 例 HCV-RNA+患者(分别来自南欧、西欧、北欧、中欧东部和东欧的 1255、970、663、633 和 787 例)中,中位随访时间为 11863 人年,有 1113 例(25.8%)开始接受任何 HCV 治疗。在至少有 F3 纤维化的患者中,所有地区超过 50%的患者未接受治疗。起始 DAA 的发生率(每 1000 人年随访,95%置信区间)从 2014 年的 7.8(5.9-9.8)增至 2015 年的 135.2(122.0-148.5)和 2016 年的 128.9(113.5-144.3)。这种增加在北欧和西欧最高,在南欧中等,在中欧东部和东欧则较为温和。调整后,女性、来自中欧东部或东欧的患者、基因型 3、未接受抗逆转录病毒治疗和 HIV-RNA 可检测的患者起始 DAA 的可能性较低。年龄较大、HCV-RNA 超过 500000IU/ml 和更严重肝纤维化的患者起始 DAA 的可能性更高。
2014 年至 2016 年间,西欧 HIV/HCV 合并感染患者 DAA 治疗的使用率显著增加,但在中欧东部和东欧地区则较为温和。在所有地区,超过 50%的至少有 F3 纤维化的患者未接受治疗。女性起始 DAA 的可能性较低。