Bonacini Maurizio, Kim Yoona, Pitney Caroline, McKoin Lee, Tran Melody, Landis Charles
Mission Gastroenterology and Hepatology, san francisco, CA, United States.
Proteus Digital Health, Redwood City, CA, United States.
J Med Internet Res. 2020 Feb 24;22(2):e15532. doi: 10.2196/15532.
A fixed-dose combination of ledipasvir/sofosbuvir (LDV/SOF) is efficacious in treating chronic hepatitis C virus (HCV) infection; however, objective adherence to prescribed regimens in real-world clinical settings has not been well studied.
This study aimed to evaluate adherence and virologic outcomes in patients with chronic HCV infection treated with LDV/SOF using a novel digital medicine program that directly measures drug ingestion adherence.
This prospective, observational, open-label, single-arm pilot study was conducted at 2 clinical research sites and followed patients with HCV infection who were prescribed LDV/SOF along with an ingestible sensor. Patients were treated for 8 or 12 weeks. The main outcomes were ingestion adherence, medical interventions, virologic response, safety, and patient satisfaction.
Of the 28 patients (mean 59 years, SD 7), 61% (17/28) were male, 61% (17/28) were non-Caucasian, and 93% (26/28) were treatment naïve. All 28 had genotype 1 HCV, and of these, 27 completed an 8- or 12-week treatment. Patients used the digital medicine program for 92% of the expected days; the overall mean ingestion adherence rate was 97%. Providers used the digital medicine program data for same-day medication therapy management in 39% (11/28) of patients. End-of-treatment response was achieved in all the available 21 of 28 patients. Sustained virologic response at 12 weeks or more was achieved in 26 of 28 patients; of the 2 patients who relapsed, one had less than 90% adherence and the other had greater than or equal to 95% adherence, lending insights into reasons for treatment failure. A total of 4 subjects reported nonserious adverse events, which were resolved.
Conclusions: The findings of this study suggest that digital medicines can be used for wirelessly observed therapy to support adherence to antiviral HCV therapy, reduce unnecessary medication wastage and retreatment costs, and potentially optimize sustained virologic response rates, especially in populations at high risk for nonadherence.
来迪派韦/索磷布韦(LDV/SOF)固定剂量组合在治疗慢性丙型肝炎病毒(HCV)感染方面疗效显著;然而,在现实临床环境中对规定治疗方案的客观依从性尚未得到充分研究。
本研究旨在使用一种直接测量药物摄入依从性的新型数字医学程序,评估接受LDV/SOF治疗的慢性HCV感染患者的依从性和病毒学结果。
这项前瞻性、观察性、开放标签、单臂试点研究在2个临床研究地点进行,对接受LDV/SOF治疗并配备可摄入传感器的HCV感染患者进行随访。患者接受8周或12周的治疗。主要结果包括摄入依从性、医疗干预、病毒学反应、安全性和患者满意度。
28名患者(平均年龄59岁,标准差7)中,61%(17/28)为男性,61%(17/28)为非白种人,93%(26/28)为初治患者。所有28名患者均为HCV基因1型,其中27名完成了8周或12周的治疗。患者使用数字医学程序的天数达到预期天数的92%;总体平均摄入依从率为97%。39%(11/28)的患者,医疗服务提供者使用数字医学程序数据进行当日药物治疗管理。28名患者中的21名可获得治疗结束时的反应。28名患者中的26名在12周或更长时间实现了持续病毒学反应;在2名复发患者中,1名患者依从性低于90%,另1名患者依从性大于或等于95%,这有助于深入了解治疗失败的原因。共有4名受试者报告了非严重不良事件,这些事件均已解决。
本研究结果表明,数字医学可用于无线观察治疗,以支持对抗病毒HCV治疗的依从性,减少不必要的药物浪费和再治疗成本,并可能优化持续病毒学反应率,特别是在依从性高风险人群中。