Effectiveness, safety/tolerability of OBV/PTV/r ± DSV in patients with HCV genotype 1 or 4 with/without HIV-1 co-infection, chronic kidney disease (CKD) stage IIIb-V and dialysis in Spanish clinical practice - Vie-KinD study

dc.contributor.authorLondoño, María Carlota
dc.contributor.authorRiveiro-Barciela, Mar
dc.contributor.authorAhumada, Adriana
dc.contributor.authorMuñoz Gómez, Raquel
dc.contributor.authorRoget, Mercé
dc.contributor.authorDevesa Medina, María J.
dc.contributor.authorSerra, Miguel Ángel
dc.contributor.authorNavascués, Carmen A.
dc.contributor.authorBaliellas Comellas, Mª Carme
dc.contributor.authorAldamiz, Teresa
dc.contributor.authorGutiérrez, María L.
dc.contributor.authorPolo Lorduy, Benjamín
dc.contributor.authorCarmona, Isabel
dc.contributor.authorBenlloch, Salvador
dc.contributor.authorBonet, Lucía
dc.contributor.authorGarcía Samaniego, Javier
dc.contributor.authorJiménez Pérez, Miguel
dc.contributor.authorMorán Sánchez, Senador
dc.contributor.authorCastro, Ángeles
dc.contributor.authorDelgado, Manuel
dc.contributor.authorGea Rodríguez, Francisco
dc.contributor.authorMartín Granizo, Ignacio
dc.contributor.authorMontes, María Luisa
dc.contributor.authorMorano, Luís
dc.contributor.authorCastaño, Manuel A.
dc.contributor.authorSantos, Ignacio de los
dc.contributor.authorLaguno Centeno, Montserrat
dc.contributor.authorLosa, Juan Emilio
dc.contributor.authorMontero-Alonso, Marta
dc.contributor.authorRivero, Antonio
dc.contributor.authorÁlvaro, Cristina de
dc.contributor.authorManzanares, Amanda
dc.contributor.authorMallolas Masferrer, Josep
dc.contributor.authorBarril, Guillermina
dc.contributor.authorGonzález Parra, Emilio
dc.contributor.authorGarcía Buey, Luisa
dc.date.accessioned2019-12-13T10:53:54Z
dc.date.available2019-12-13T10:53:54Z
dc.date.issued2019-09-24
dc.date.updated2019-12-10T08:21:10Z
dc.description.abstractLimited data are available on the effectiveness and tolerability of direct-acting antivirals (DAAs) therapies in the real world for HCV-infected patients with comorbidities. This study aimed to describe the effectiveness of OBV/PTV/r ± DSV (3D/2D regimen) with or without ribavirin (RBV) in HCV or HCV/HIV co-infected patients with GT1/GT4 and CKD (IIIb-V stages), including those under hemodialysis and peritoneal dialysis in routine clinical practice in Spain in 2015.Non-interventional, retrospective, multicenter data collection study in 31 Spanish sites. Socio-demographic, clinical variables, study treatment characteristics, effectiveness and tolerability data were collected from medical records.Data from 135 patients with a mean age (SD) of 58.3 (11.4) years were analyzed: 92.6% GT1 (81.6% GT1b and 17.6% GT1a) and 7.4% GT4, 14 (10.4%) HIV/HCV co-infected, 19.0% with fibrosis F3 and 28.1% F4 by FibroScan®, 52.6% were previously treated with pegIFN and RBV. 11.1%, 14.8% and 74.1% of patients had CKD stage IIIb, IV and V respectively. 68.9% of patients were on hemodialysis; 8.9% on peritoneal dialysis and 38.5% had history of renal transplant. A total of 125 (96.2%) of 135 patients were treated with 3D, 10 (7.4%) with 2D and 30.4% received RBV. The overall intention-to-treat (ITT) sustained virologic response at week 12 (SVR12) was 92.6% (125/135) and the overall modified-ITT (mITT) SVR12 was 99.2% (125/126). The SVR12 rates (ITT) per sub-groups were: HCV mono-infected (91.7%), HCV/HIV co-infected (100%), GT1 (92.0%), GT4 (100%), CKD stage IIIb (86.7%), stage IV (95%) and stage V (93%). Among the 10 non-SVR there was only 1 virologic failure (0.7%); 4 patients had missing data due lost to follow up (3.0%) and 5 patients discontinued 3D/2D regimen (3.7%): 4 due to severe adverse events (including 3 deaths) and 1 patient´s decision.These results have shown that 3D/2D regimens are effective and tolerable in patients with advanced CKD including those in dialysis with GT 1 or 4 chronic HCV mono-infection and HIV/HCV coinfection in a real-life cohort. The overall SVR12 rates were 92.6% (ITT) and 99.2% (mITT) without clinically relevant changes in eGFR until 12 weeks post-treatment. These results are consistent with those reported in clinical trials.
dc.format.extent14 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idimarina5865124
dc.identifier.issn1932-6203
dc.identifier.pmid31550267
dc.identifier.urihttps://hdl.handle.net/2445/146637
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1371/journal.pone.0221567
dc.relation.ispartofPLoS One, 2019, vol. 14, num. 9, p. e0221567
dc.relation.urihttps://doi.org/10.1371/journal.pone.0221567
dc.rightscc by (c) Londoño et al., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationMalalties del ronyó
dc.subject.classificationHepatitis C
dc.subject.otherKidney diseases
dc.titleEffectiveness, safety/tolerability of OBV/PTV/r ± DSV in patients with HCV genotype 1 or 4 with/without HIV-1 co-infection, chronic kidney disease (CKD) stage IIIb-V and dialysis in Spanish clinical practice - Vie-KinD study
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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