在澳大利亚艾滋病毒感染者中向丙型肝炎微消除迈进:停止研究。

M. Martinello, J. Yee, S. Bartlett, P. Read, D. Baker, J. Post, R. Finlayson, M. Bloch, J. Doyle, D. Shaw, M. Hellard, K. Petoumenos, Lanni Lin, P. Marks, T. Applegate, G. Dore, G. Matthews
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引用次数: 37

摘要

从2016年开始,直接作用抗病毒(DAA)治疗可以不受限制地获得,在澳大利亚HIV感染者中微消除HCV可能是可行的。我们的目的是评估在普遍获得DAA后,澳大利亚HIV/HCV合并感染成人在消除目标方面的进展。方法:该前瞻性队列研究招募了来自澳大利亚14家初级和三级诊所的HIV/HCV阳性成年人,无论病毒状态如何。评估年度和累计HCV治疗的接受情况、结果和HCV RNA流行情况,随访至2018年5月(中位随访:2.63年)。分析与DAA摄取相关的因素。结果2014年7月至2017年3月,共纳入402例HIV/HCV抗体阳性受试者(95%为男性[80%为男同性恋和双性恋男性],13%为肝硬化,80%为注射吸毒史[39%为注射史])。在普遍获得DAA后,符合条件的丙型肝炎病毒治疗的年接受率分别从2014年和2015年的7%和11%增加到2016年的80%。到2018年,有资格接受治疗的丙型肝炎患者的累计接受治疗率为91%(336/371)。HCV病毒血症患病率从2014年的82% (95%CI 78%, 86%)下降到2018年的8% (95%CI 6%, 12%)。再感染发生率为0.81 / 100人年(95% CI 0.34, 1.94),仅有5名参与者报告再感染。结论:在澳大利亚,无限制DAA疗法的高吸收率和有效性使得治疗规模迅速扩大,显著降低了HCV感染负担,HIV感染者的再感染率也很低,这表明微消除是可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Moving towards hepatitis C micro-elimination among people living with HIV in Australia: the CEASE study.
BACKGROUND Micro-elimination of HCV among people living with HIV may be feasible in Australia, given unrestricted access to direct-acting antiviral (DAA) therapy from 2016. Our aim was to evaluate progress towards elimination goals within HIV/HCV co-infected adults in Australia following universal DAA access. METHODS The CEASE prospective cohort study enrolled HIV/HCV positive adults, irrespective of viremic status, from 14 primary and tertiary clinics in Australia. Annual and cumulative HCV treatment uptake, outcome, and HCV RNA prevalence were evaluated, with follow-up through May 2018 (median follow-up: 2.63 years). Factors associated with DAA uptake were analysed. RESULTS Between July 2014 and March 2017, 402 HIV/HCV antibody-positive participants were enrolled (95% male [80% gay and bisexual men,], 13% cirrhosis, 80% history of injecting drug use [39% current injecting]). Following universal DAA access, annual HCV treatment uptake in those eligible increased from 7% and 11% per year in 2014 and 2015, respectively, to 80% in 2016. By 2018, cumulative HCV treatment uptake in those ever eligible for treatment was 91% (336/371). HCV viremic prevalence declined from 82% (95%CI 78%, 86%) in 2014 to 8% (95%CI 6%, 12%) in 2018. Reinfection was reported in only five participants for a reinfection incidence of 0.81 per 100-person years (95% CI 0.34, 1.94). CONCLUSIONS High uptake and effectiveness of unrestricted DAA therapy in Australia has permitted rapid treatment scale-up, with a dramatic reduction in HCV infection burden and low reinfection rate among people living with HIV, suggesting that micro-elimination is feasible.
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