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| dc.contributor.author | Belén-Pérez, Ana | |
| dc.contributor.author | Chueca, Natalia | |
| dc.contributor.author | Macias, Juan | |
| dc.contributor.author | Pineda, Juan-Antonio | |
| dc.contributor.author | Salmeron, Javier | |
| dc.contributor.author | Rivero-Juarez, Antonio | |
| dc.contributor.author | Hidalgo-Tenorio, Carmen | |
| dc.contributor.author | Espinosa, María-Dolores | |
| dc.contributor.author | Tellez, Francisco | |
| dc.contributor.author | von-Wichmann, Miguel-Ángel | |
| dc.contributor.author | Omar, Mohamed | |
| dc.contributor.author | Santos, Jesús | |
| dc.contributor.author | Hernández-Quero, José | |
| dc.contributor.author | Joaquin-Anton, José | |
| dc.contributor.author | Collado, Antonio | |
| dc.contributor.author | Belén-Lozano, Ana | |
| dc.contributor.author | García-Deltoro, Miguel | |
| dc.contributor.author | Casado, Marta | |
| dc.contributor.author | Pascasio, Juan-Manuel | |
| dc.contributor.author | Selfa, Aida | |
| dc.contributor.author | Miguel-Rosales, José | |
| dc.contributor.author | de-la-Iglesia, Alberto | |
| dc.contributor.author | Ignacio-Arenas, Juan | |
| dc.contributor.author | García-Bujalance, Silvia | |
| dc.contributor.author | Rios, María-José | |
| dc.contributor.author | Bernal-Morell, Enrique | |
| dc.contributor.author | Martínez, Onofre | |
| dc.contributor.author | García-Herola, Antonio | |
| dc.contributor.author | Velez, Mónica | |
| dc.contributor.author | Rincon, Pilar | |
| dc.contributor.author | García, Federico | |
| dc.date.accessioned | 2026-01-19T16:05:32Z | |
| dc.date.available | 2026-01-19T16:05:32Z | |
| dc.date.issued | 2019-08-30 | |
| dc.identifier.citation | Pérez AB, Chueca N, Macías J, Pineda JA, Salmerón J, Rivero-Juárez A, et al. Prevalence of resistance associated substitutions and efficacy of baseline resistance-guided chronic hepatitis C treatment in Spain from the GEHEP-004 cohort. Kanda T, editor. PLoS ONE. 30 de agosto de 2019;14(8):e0221231. | |
| dc.identifier.issn | 1932-6203 | |
| dc.identifier.uri | https://sms.carm.es/ricsmur/handle/123456789/23713 | |
| dc.description.abstract | Treatment guidelines differ in their recommendation to determine baseline resistance associated substitutions (RAS) before starting a first-line treatment with direct-acting antivirals (DAAs). Here we analyze the efficacy of DAA treatment with baseline RAS information. We conducted a prospective study involving 23 centers collaborating in the GEHEP-004 DAA resistance cohort. Baseline NS5A and NS3 RASs were studied by Sanger sequencing. After issuing a comprehensive resistance report, the treating physician decided the therapy, duration and ribavirin use. Sustained virological response (SVR12) data are available in 275 patients. Baseline NS5A RAS prevalence was between 4.3% and 26.8% according to genotype, and NS3 RASs prevalence (GT1a) was 6.3%. Overall, SVR12 was 97.8%. Amongst HCV-GT1a patients, 75.0% had >800,000 IU/ml and most of those that started grazoprevir/elbasvir were treated for 12 weeks. In genotype 3, NS5A Y93H was detected in 9 patients. 42.8% of the HCV-GT3 patients that started sofosbuvir/velpatasvir included ribavirin, although only 14.7% carried Y93H. The efficacy of baseline resistance-guided treatment in our cohort has been high across the most prevalent HCV genotypes in Spain. The duration of the grazoprevir/elbasvir treatment adhered mostly to AASLD/IDSA recommendations. In cirrhotic patients infected with GT-3 there has been a high use of ribavirin. | |
| dc.language.iso | eng | |
| dc.publisher | PUBLIC LIBRARY SCIENCE | |
| dc.rights | Atribución/Reconocimiento 4.0 Internacional | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/deed.es | * |
| dc.subject.mesh | Amides | |
| dc.subject.mesh | Antiviral Agents/adverse effects/therapeutic use | |
| dc.subject.mesh | Benzofurans/therapeutic use | |
| dc.subject.mesh | Carbamates | |
| dc.subject.mesh | Cyclopropanes | |
| dc.subject.mesh | Drug Resistance, Viral/genetics | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Genotype | |
| dc.subject.mesh | Hepacivirus/genetics/pathogenicity | |
| dc.subject.mesh | Hepatitis C, Chronic/drug therapy/epidemiology/genetics/virology | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Imidazoles/therapeutic use | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Mutation | |
| dc.subject.mesh | Quinoxalines/therapeutic use | |
| dc.subject.mesh | Ribavirin/therapeutic use | |
| dc.subject.mesh | Sofosbuvir/therapeutic use | |
| dc.subject.mesh | Spain/epidemiology | |
| dc.subject.mesh | Sulfonamides | |
| dc.subject.mesh | Sustained Virologic Response | |
| dc.subject.mesh | Viral Nonstructural Proteins/genetics | |
| dc.title | Prevalence of resistance associated substitutions and efficacy of baseline resistance-guided chronic hepatitis C treatment in Spain from the GEHEP-004 cohort | |
| dc.type | info:eu-repo/semantics/article | |
| dc.identifier.pmid | 31469856 | |
| dc.relation.publisherversion | https://dx.plos.org/10.1371/journal.pone.0221231 | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dc.identifier.doi | 10.1371/journal.pone.0221231 | |
| dc.journal.title | Plos One |