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Real‐world use of elbasvir‐grazoprevir in patients with chronic hepatitis C: retrospective analyses from the TRIO TRIO network

机译:真实世界使用Elbasvir-Grazopherir在慢性丙型肝炎患者中的患者:从三重奏网络中的回顾性分析

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Summary Background Elbasvir‐grazoprevir is indicated for chronic hepatitis C virus ( HCV ) genotypes 1 and 4. Aim To evaluate the utilization and outcomes of chronic HCV patients treated with elbasvir‐grazoprevir in the United States. Methods We conducted a retrospective cohort study of adults treated with elbasvir‐grazoprevir with or without ribavirin for chronic HCV genotypes 1 or 4 infection. Data were collected from healthcare providers and specialty pharmacies through Innervation Platform, a proprietary, cloud‐based disease management program from Trio Health. The primary endpoint was per protocol sustained virological response 12 weeks post‐treatment ( SVR 12). Results Among 470 patients treated in 2016, 95% had HCV genotype 1 infection, 80% (373/468) were HCV treatment na?ve and 70% (327/468) had non‐cirrhotic disease. Almost 3 quarters (73%) of patients received care in community practices. The majority (89%) of patients received elbasvir‐grazoprevir for 12 weeks. Per protocol SVR 12 rates were 99% (396/402) for HCV genotype 1 and 95% (21/22) for HCV genotype 4. Among patients with Stage 4 or 5 chronic kidney diseases, 99% (113/114) achieved SVR 12. In univariate analyses, variables significantly associated with per protocol SVR 12 for the entire sample were therapy duration ( P = 0.001), treatment experience ( P = 0.016), and cirrhosis status ( P = 0.001). However, among HCV genotype 1 patients, no variables were significant. Intent‐to‐treat SVR 12 rates were 89% (396/447) for HCV genotype 1 and 91% (21/23) for HCV genotype 4. Conclusion Elbasvir‐grazoprevir is highly effective, and in this 2016 cohort, its use was predominantly in patients with HCV genotype 1 and as a 12‐week therapy without ribavirin.
机译:发明内容背景Elbasvir-Grazoprevir针对慢性丙型肝炎病毒(HCV)基因型1和4表示。旨在评估用美国Elbasvir-Grazopherir治疗的慢性HCV患者的利用和结果。方法我们对慢性HCV基因型1或4感染的慢性HCV基因素治疗的Elbasvir-Grazoprevir治疗的成人进行了回顾性队列研究。通过支撑平台,专有的云的疾病管理计划从医疗保健提供者和特种药店收集数据,从三重奏健康。初级终点是每种协议治疗后12周持续的病毒学响应(SVR 12)。结果2016年治疗470名患者中,95%有HCV基因型1感染,80%(373/468)是HCV治疗Na'Ve,70%(327/468)具有非肝硬化疾病。近3个季度(73%)患者在社区实践中受到护理。大多数(89%)患者接受了Elbasvir-Grazopher 12周。对于HCV基因型1和95%(21/22),每种协议SVR 12率为99%(396/402),用于HCV基因型4.患有阶段4或5慢性肾脏疾病的患者,99%(113/114)达到SVR 12.在单变量分析中,对于整个样品的每种协议SVR 12显着相关的变量是治疗持续时间(p = 0.001),治疗经验(p = 0.016)和肝硬化状态(p = 0.001)。然而,在HCV基因型1例中,没有变量是显着的。对于HCV基因型1和91%(21/23)的HCV基因型4.结论Elbasvir-Grazoprevir是89%的SVR 12速率为89%(396/447),并且在本2016年的队列中,其使用主要是HCV基因型1患者,作为没有利巴韦林的12周的治疗。

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    Northwestern University Feinberg School of MedicineChicago IL USA;

    Saint Louis University School of MedicineSt. Louis MO USA;

    Beth Israel Deaconess Medical CenterBoston MA USA;

    Trio Health AnalyticsLa Jolla CA USA;

    Merck &

    Co. Inc.Kenilworth NJ USA;

    Queens Medical CenterUniversity of HawaiiHonolulu HI USA;

    Department of MedicineInova Fairfax HospitalFalls Church VA USA;

    Beth Israel Deaconess Medical CenterBoston MA USA;

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  • 正文语种 eng
  • 中图分类 药理学;
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