Publication: A Predictive Model for Selecting Patients with HCV Genotype 3 Chronic Infection with a High Probability of Sustained Virological Response to Peginterferon Alfa-2a/Ribavirin.
dc.contributor.author | Asselah, Tarik | |
dc.contributor.author | Thompson, Alex J | |
dc.contributor.author | Flisiak, Robert | |
dc.contributor.author | Romero-Gomez, Manuel | |
dc.contributor.author | Messinger, Diethelm | |
dc.contributor.author | Bakalos, Georgios | |
dc.contributor.author | Shiffman, Mitchell L | |
dc.date.accessioned | 2023-01-25T08:31:25Z | |
dc.date.available | 2023-01-25T08:31:25Z | |
dc.date.issued | 2016-03-18 | |
dc.description.abstract | Access to direct-acting antiviral agents (DAAs) is restricted in some settings; thus, the European Association for the Study of the Liver recommends dual peginterferon/ribavirin (PegIFN/RBV) therapy wherever DAAs are unavailable. HCV genotype (GT) 3 infection is now the most difficult genotype to eradicate and PegIFN/RBV remains an effective option. The goal of this study was to devise a simple predictive score to identify GT3 patients with a high probability of achieving a sustained virologic response (SVR) with PegIFN alfa-2a/RBV therapy. Relationships between baseline characteristics and SVR were explored by multiple logistic regression models and used to develop a simple scoring system to predict SVR using data from 1239 treatment-naive GT3 patients who received PegIFN alfa-2a/RBV for 24 weeks in two large observational cohort studies. The score was validated using a database of 473 patients. Scores were assigned for six factors as follows: age (years) (≤40: 2 points; >40 but ≤55: 1); bodyweight (kg) (40 but ≤55: 1); bodyweight (kg) (200: 2; ≥100 but A simple baseline scoring system involving age, bodyweight, cirrhosis status, ALT level, platelet count and HCV RNA level can be used to identify treatment-naive Caucasian patients with HCV GT3 infection with a high probability of SVR with PegIFN alfa-2a/RBV therapy. | |
dc.identifier.doi | 10.1371/journal.pone.0150569 | |
dc.identifier.essn | 1932-6203 | |
dc.identifier.pmc | PMC4798721 | |
dc.identifier.pmid | 26991780 | |
dc.identifier.pubmedURL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4798721/pdf | |
dc.identifier.unpaywallURL | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0150569&type=printable | |
dc.identifier.uri | http://hdl.handle.net/10668/9928 | |
dc.issue.number | 3 | |
dc.journal.title | PloS one | |
dc.journal.titleabbreviation | PLoS One | |
dc.language.iso | en | |
dc.organization | Área de Gestión Sanitaria Sur de Sevilla | |
dc.organization | Área de Gestión Sanitaria Sur de Sevilla | |
dc.organization | AGS - Sur de Sevilla | |
dc.organization | AGS - Sur de Sevilla | |
dc.page.number | e0150569 | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.pubmedtype | Validation Study | |
dc.rights | Attribution 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject.mesh | Adolescent | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Antiviral Agents | |
dc.subject.mesh | Female | |
dc.subject.mesh | Genotype | |
dc.subject.mesh | Hepacivirus | |
dc.subject.mesh | Hepatitis C, Chronic | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Interferon-alpha | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Models, Theoretical | |
dc.subject.mesh | Polyethylene Glycols | |
dc.subject.mesh | Recombinant Proteins | |
dc.subject.mesh | Retrospective Studies | |
dc.subject.mesh | Ribavirin | |
dc.subject.mesh | Viral Load | |
dc.subject.mesh | Young Adult | |
dc.title | A Predictive Model for Selecting Patients with HCV Genotype 3 Chronic Infection with a High Probability of Sustained Virological Response to Peginterferon Alfa-2a/Ribavirin. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 11 | |
dspace.entity.type | Publication |
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