Publication:
Darunavir/cobicistat showing similar effectiveness as darunavir/ritonavir monotherapy despite lower trough concentrations.

dc.contributor.authorGutierrez-Valencia, Alicia
dc.contributor.authorTrujillo-Rodriguez, Maria
dc.contributor.authorFernandez-Magdaleno, Tamara
dc.contributor.authorEspinosa, Nuria
dc.contributor.authorViciana, Pompeyo
dc.contributor.authorLópez-Cortés, Luis F
dc.date.accessioned2023-01-25T10:03:39Z
dc.date.available2023-01-25T10:03:39Z
dc.date.issued2018
dc.description.abstractWhen 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 ). 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. 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). 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.identifier.doi10.1002/jia2.25072
dc.identifier.essn1758-2652
dc.identifier.pmcPMC5808101
dc.identifier.pmid29430854
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808101/pdf
dc.identifier.unpaywallURLhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/jia2.25072
dc.identifier.urihttp://hdl.handle.net/10668/12115
dc.issue.number2
dc.journal.titleJournal of the International AIDS Society
dc.journal.titleabbreviationJ Int AIDS Soc
dc.language.isoen
dc.organizationIBIS
dc.pubmedtypeJournal Article
dc.pubmedtypeObservational Study
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCtrough
dc.subjectDarunavir
dc.subjectcobicistat
dc.subjectmonotherapy
dc.subjectpharmacokinetic
dc.subjectritonavir
dc.subject.meshAdult
dc.subject.meshAnti-HIV Agents
dc.subject.meshCobicistat
dc.subject.meshDarunavir
dc.subject.meshDrug Therapy, Combination
dc.subject.meshFemale
dc.subject.meshHIV Infections
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshProspective Studies
dc.subject.meshReverse Transcriptase Inhibitors
dc.subject.meshRitonavir
dc.subject.meshViral Load
dc.titleDarunavir/cobicistat showing similar effectiveness as darunavir/ritonavir monotherapy despite lower trough concentrations.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number21
dspace.entity.typePublication

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