Evidence map›Paper›PMID 39470876›Full record

Observational studyAdvances in therapy2024

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 and 20 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Advances in therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors.

Markus CornbergDepartment of Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany. cornberg.markus@mh-hannover.de.ORCID 0000-0002-9141-8001
Dietrich HüppeGastroenterologische Gemeinschaftspraxis Herne, Herne, Germany.
Christoph SarrazinDepartment of Internal Medicine and Liver Center, St. Josefs-Hospital Wiesbaden and Viral Hepatitis Research Group, Goethe-University Hospital Frankfurt, Frankfurt, Germany.
Adriana AhumadaLiver Unit, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Francisco Jorquera PlazaDigestive System Service, Complejo Asistencial Universitario de León, IBIOMED and CIBERehd, León, Spain.
Zoe MariñoHospital Clínic, IDIBAPS, CIBERehd, Universitat de Barcelona, Barcelona, Spain.
Juan Isidro Uriz OtanoNavarra Institute for Health Research (IdiSNA), Pamplona, Spain.
Brian ConwayVancouver Infectious Diseases Center, Simon Fraser University, Vancouver, BC, Canada.
Lindsay MylesBarrie GI Associates, Barrie, ON, Canada.
Alnoor RamjiUniversity of British Columbia, Vancouver, BC, Canada.
Armand AbergelDépartement de Médecine Digestive, CHU Estaing, Clermont-Ferrand, France.
Tarik AsselahDepartment of Hepatology, AP-HP Hôpital Beaujon, Université de Paris, Cité CRI, INSERM UMR 1149, Clichy, France.
Dominique LarreyService des maladies de l'appareil digestif, Hôpital Saint Eloi and IBR, INSERM, Montpellier, France.
Alessio AghemoDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Massimo AndreoniUniversity of Tor Vergata, Rome, Italy.
Antonio GasbarriniInternal Medicine and Gastroenterology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Pietro LamperticoOspedale Maggiore Policlinico, Policlinico, Division of Gastroenterology and Hepatology, CRC 'AM and A Migliavacca' Centre for Liver Disease, Foundation IRCCS Ca' Granda, Milan, Italy.
Marcello PersicoDipartimento di Medicina Clinica Medica, Epatologica e Lungodegenza, AOU OO. RR. San Giovanni di dio Ruggi e D'Aragona, Salerno, Italy.
Erica VillaUC Gastroenterologia, Dipartimento di Specialità Mediche, Azienda Ospedaliera Universitaria di Modena, Modena, Italy.
Michal CarmielLiver Unit, Galilee Medical Center, Nahariya, Israel.
Gabriel ChodickMaccabitech, Maccabi Healthcare Services, Tel-Aviv, Israel.
Clara WeilMaccabitech, Maccabi Healthcare Services, Tel-Aviv, Israel.
Abhi BhagatAbbVie Inc., North Chicago, IL, USA.
Mark BondinAbbVie Inc., North Chicago, IL, USA.
Isabel ButrymowiczAbbVie Inc., North Chicago, IL, USA.
Yanna SongAbbVie Inc., North Chicago, IL, USA.
Dimitri SemizarovAbbVie Inc., North Chicago, IL, USA.
Sadhana SonparoteAbbVie Inc., North Chicago, IL, USA.
Cynthia LlamasAbbVie Inc., North Chicago, IL, USA.
CREST Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis 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.

methodsAnalysis 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.

resultsThe 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.

conclusionThis 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.

Indexed as

Antiviral AgentsBenzimidazolesHepatitis C, ChronicLiver CirrhosisPyrrolidinesQuinoxalinesSulfonamidesAdultAgedAminoisobutyric AcidsCyclopropanesDrug CombinationsFemaleHumansLactams, MacrocyclicLeucineAminoisobutyric AcidsAntiviral AgentsBenzimidazolesCyclopropanesDrug Combinationsglecaprevirglecaprevir and pibrentasvirLactams, MacrocyclicLeucinepibrentasvirProlinePyrrolidinesQuinoxalinesSulfonamidesCompensated cirrhosisDirect-acting antiviralsHepatitis C virusReal worldTreatment-naïve

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.