Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Saint Louis University School of Medicine, St. Louis, MO, USA.
Aliment Pharmacol Ther. 2018 Jun;47(11):1511-1522. doi: 10.1111/apt.14635. Epub 2018 Apr 17.
Elbasvir-grazoprevir is indicated for chronic hepatitis C virus (HCV) genotypes 1 and 4.
To evaluate the utilization and outcomes of chronic HCV patients treated with elbasvir-grazoprevir in the United States.
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 (SVR12).
Among 470 patients treated in 2016, 95% had HCV genotype 1 infection, 80% (373/468) were HCV treatment naïve 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 SVR12 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 SVR12. In univariate analyses, variables significantly associated with per protocol SVR12 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 SVR12 rates were 89% (396/447) for HCV genotype 1 and 91% (21/23) for HCV genotype 4.
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.
Elbasvir-grazoprevir 被批准用于治疗慢性丙型肝炎病毒(HCV)基因型 1 和 4。
评估美国使用 Elbasvir-grazoprevir 治疗慢性 HCV 患者的效果和结局。
我们进行了一项回顾性队列研究,纳入了接受 Elbasvir-grazoprevir 联合或不联合利巴韦林治疗慢性 HCV 基因型 1 或 4 感染的成年人。数据来自于 Innervation 平台,该平台是 Trio Health 的一个专有、基于云的疾病管理项目,从医疗保健提供者和专科药房收集。主要终点是治疗后 12 周的持续病毒学应答 12 周(SVR12)。
在 2016 年接受治疗的 470 名患者中,95%的患者为 HCV 基因型 1 感染,80%(373/468)为 HCV 初治患者,70%(327/468)为非肝硬化疾病。近 3 分之 4(73%)的患者在社区诊所接受治疗。大多数(89%)患者接受 Elbasvir-grazoprevir 治疗 12 周。HCV 基因型 1 的 SVR12 率为 99%(396/402),HCV 基因型 4 的 SVR12 率为 95%(21/22)。在慢性肾脏病 4 或 5 期的患者中,99%(113/114)达到 SVR12。在单变量分析中,与整个样本的 SVR12 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 患者中,没有变量具有显著意义。HCV 基因型 1 的意向治疗 SVR12 率为 89%(396/447),HCV 基因型 4 的 SVR12 率为 91%(21/23)。
Elbasvir-grazoprevir 非常有效,在 2016 年的队列中,它主要用于 HCV 基因型 1 患者,且作为一种无利巴韦林的 12 周治疗方案。