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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
Article de revue scientifique   Avec comité de lecture

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

Markus Cornberg, Dietrich Hüppe, Christoph Sarrazin, Adriana Ahumada, Francisco Jorquera Plaza, Zoe Mariño, Juan Isidro Uriz Otano, Brian Conway, Lindsay Myles, Alnoor Ramji, …
Advances in therapy, Vol.41(12), p.4669-4682
01/12/2024
PMID: 39470876

Résumé

Adult Aged Aminoisobutyric Acids Antiviral Agents - adverse effects Antiviral Agents - therapeutic use Benzimidazoles - adverse effects Benzimidazoles - therapeutic use Cyclopropanes Drug Combinations Female Hepatitis C, Chronic - complications Hepatitis C, Chronic - drug therapy Humans Lactams, Macrocyclic Leucine - analogs & derivatives Liver Cirrhosis - drug therapy Male Middle Aged Proline - analogs & derivatives Pyrrolidines - therapeutic use Quinoxalines - adverse effects Quinoxalines - therapeutic use Retrospective Studies Sulfonamides - adverse effects Sulfonamides - therapeutic use Sustained Virologic Response Treatment Outcome
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. 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. 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. 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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