Updated Results from the Retrospective CREST Study on the Safety and Effectiveness of 8-Week Glecaprevir/Pibrentasvir in HCV-Infected Treatment-Naïve Patients with Compensated Cirrhosis

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Advances in Therapy Pub Date : 2024-10-29 DOI:10.1007/s12325-024-02996-6
Markus Cornberg, Dietrich Hüppe, Christoph Sarrazin, Adriana Ahumada, Francisco Jorquera Plaza, Zoe Mariño, Juan Isidro Uriz Otano, Brian Conway, Lindsay Myles, Alnoor Ramji, Armand Abergel, Tarik Asselah, Dominique Larrey, Alessio Aghemo, Massimo Andreoni, Antonio Gasbarrini, Pietro Lampertico, Marcello Persico, Erica Villa, Michal Carmiel, Gabriel Chodick, Clara Weil, Abhi Bhagat, Mark Bondin, Isabel Butrymowicz, Yanna Song, Dimitri Semizarov, Sadhana Sonparote, Cynthia Llamas, The CREST Study Group
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Abstract

Introduction

This brief report presents updated findings from the previously published CREST study evaluating the safety and effectiveness of 8-week glecaprevir/pibrentasvir (GLE/PIB) in treatment-naïve patients with chronic hepatitis C virus (HCV) infection and compensated cirrhosis. The current study includes an additional 51 patients, presents effectiveness data stratified by additional comorbidities and comedications, and offers insights into healthcare resource utilization.

Methods

Analysis of treatment-naïve patients with HCV infection and compensated cirrhosis enrolled in the CREST study, a real-world, observational multicenter study. All enrolled patients were included in the full analysis set (FAS); the modified analysis set (MAS) excluded patients with missing SVR12 data, or who discontinued GLE/PIB for nonvirologic failure. The primary endpoint was sustained virologic response at posttreatment week 12 (SVR12) in the MAS. Safety and healthcare resource utilization were also assessed.

Results

The FAS included 437 patients, and the MAS 375. Overall, the results were consistent with the previously published study, with 98.9% of patients in the MAS achieving SVR12. Patients with comorbidities such as alcoholism, diabetes, and hyperlipidemia achieved SVR12 rates > 94%. High SVR12 rates were also achieved by patients receiving comedications such as anxiolytics, antidepressants, and opioid agonists. Of the 26.8% of patients with an adverse event, 1.1% had a serious adverse event, none of which were deemed related to GLE/PIB. Healthcare resource utilization varied by employment status and history of drug use. Active drug users had more physician and nurse visits than specialist visits compared with former drug users.

Conclusion

This study provides further evidence on the safety and effectiveness of 8-week GLE/PIB, supporting the use of shorter treatment in treatment-naïve patients with Child–Pugh A cirrhosis including subgroups of interest, regardless of comorbidities and comedications observed in this population. The variable healthcare resource utilization in different patient types can help plan and resource linkage to care better, thus supporting HCV elimination efforts.

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8周Glecaprevir/Pibrentasvir治疗HCV感染的肝硬化代偿期治疗新患者的安全性和有效性回顾性CREST研究的最新结果。
简介:本简要报告介绍了之前发表的 CREST 研究的最新结果,该研究评估了格列卡韦/匹布特韦(GLE/PIB)对慢性丙型肝炎病毒(HCV)感染和代偿性肝硬化的治疗无效患者进行为期 8 周治疗的安全性和有效性。目前的研究新增了 51 例患者,根据其他合并症和合并用药提供了疗效数据,并对医疗资源利用情况进行了深入分析:方法:对参加 CREST 研究(一项真实世界的多中心观察性研究)的 HCV 感染和代偿期肝硬化的治疗无效患者进行分析。所有入组患者均纳入完整分析集(FAS);修正分析集(MAS)排除了 SVR12 数据缺失或因非病毒学失败而停止 GLE/PIB 的患者。在 MAS 中,主要终点是治疗后第 12 周的持续病毒学应答(SVR12)。此外,还对安全性和医疗资源利用率进行了评估:FAS纳入了437名患者,MAS纳入了375名患者。总体而言,研究结果与之前发表的研究结果一致,MAS 中 98.9% 的患者达到了 SVR12。酗酒、糖尿病和高脂血症等合并症患者的 SVR12 成功率大于 94%。接受抗焦虑药、抗抑郁药和阿片类受体激动剂等治疗的患者的 SVR12 率也很高。在发生不良事件的 26.8% 患者中,1.1% 的患者发生了严重不良事件,其中无一被认为与 GLE/PIB 有关。医疗资源利用率因就业状况和吸毒史而异。与以前的吸毒者相比,现在的吸毒者看医生和护士的次数多于看专科医生的次数:本研究进一步证明了8周GLE/PIB的安全性和有效性,支持对Child-Pugh A肝硬化治疗无效的患者(包括感兴趣的亚组)采用更短的治疗时间,而不考虑在该人群中观察到的合并症和合并用药。不同类型患者对医疗资源的利用情况各不相同,这有助于更好地规划和利用医疗资源,从而支持消除丙型肝炎病毒的工作。
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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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