Publication: Darunavir/cobicistat showing similar effectiveness as darunavir/ritonavir monotherapy despite lower trough concentrations.
| dc.contributor.author | Gutierrez-Valencia, Alicia | |
| dc.contributor.author | Trujillo-Rodriguez, Maria | |
| dc.contributor.author | Fernandez-Magdaleno, Tamara | |
| dc.contributor.author | Espinosa, Nuria | |
| dc.contributor.author | Viciana, Pompeyo | |
| dc.contributor.author | López-Cortés, Luis F | |
| dc.date.accessioned | 2024-10-23T09:55:47Z | |
| dc.date.available | 2024-10-23T09:55:47Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | Introduction: When darunavir (DRV) 800 mg is boosted with 150 mg cobicistat (DRVcobi), DRV trough concentration (Ctrough) is about 30% lower as compared to 100 mg ritonavir (DRVrtv). DRVcobi shows similar virological efficacy as DRVrtv when combined with two nucleos(t)ide analogue reverse-transcriptase inhibitors, but it is unknown whether a lower DRV Ctrough would undermine the effectiveness of DRVcobi when given as monotherapy (mtDRVcobi). Methods: Prospective observational study on virologically suppressed HIV-infected subjects who switched to mtDRVcobi . Virological failure was defined as two consecutive HIV-RNA >200 copies/mL. Efficacy was evaluated by intention-to-treat (ITT) and on-treatment (OT) analyses, and compared with data from a previous cohort of subjects on mtDRVrtv conducted at our centre. Plasma DRV Ctrough was measured using LC-MS/MS. Results: A total of 234 subjects were enrolled. At week 96, the efficacy rates were 67.8% (CI95 , 61.8 to 73.7) by ITT and 86.9% (CI95 , 78.0 to 87.7) by OT analyses. The corresponding rates in our historical DRVrtv controls were 67.6% (CI95 , 60.0 to 75.2) and 83.6% (CI95 : 77.2 to 90.0). A total of 135 DRV determinations were performed in 83 subjects throughout the follow-up period, with a median plasma DRV Ctrough of 1305 ng/mL (range, 150 to 5895) compared with 1710 ng/mL (range, 200 to 3838) in subjects on monotherapy with DRVrtv (p = 0.05). Conclusions: DRV Ctrough was lower in HIV-infected subjects receiving DRVcobi than with DRVrtv . However, this did not appear to influence the efficacy of DRVcobi , when administered as monotherapy. | |
| dc.format.number | 2 | es_ES |
| dc.format.volume | 21 | es_ES |
| dc.identifier.doi | 10.1002/jia2.25072 | |
| dc.identifier.e-issn | 1758-2652 | es_ES |
| dc.identifier.journal | Journal of the International AIDS Society | es_ES |
| dc.identifier.other | http://hdl.handle.net/10668/12115 | |
| dc.identifier.pubmedID | 29430854 | es_ES |
| dc.identifier.uri | https://hdl.handle.net/20.500.12105/25242 | |
| dc.language.iso | eng | |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Attribution 4.0 International | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | Ctrough | |
| dc.subject | Darunavir | |
| dc.subject | Cobicistat | |
| dc.subject | Monotherapy | |
| dc.subject | Pharmacokinetic | |
| dc.subject | Ritonavir | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Anti-HIV Agents | |
| dc.subject.mesh | Cobicistat | |
| dc.subject.mesh | Darunavir | |
| dc.subject.mesh | Drug Therapy, Combination | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | HIV Infections | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Prospective Studies | |
| dc.subject.mesh | Reverse Transcriptase Inhibitors | |
| dc.subject.mesh | Ritonavir | |
| dc.subject.mesh | Viral Load | |
| dc.title | Darunavir/cobicistat showing similar effectiveness as darunavir/ritonavir monotherapy despite lower trough concentrations. | |
| dc.type | research article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication |


