Source:http://linkedlifedata.com/resource/pubmed/id/20507207
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rdf:type | |
lifeskim:mentions |
umls-concept:C0009452,
umls-concept:C0012655,
umls-concept:C0019682,
umls-concept:C0019699,
umls-concept:C0030705,
umls-concept:C0332307,
umls-concept:C0439230,
umls-concept:C0441655,
umls-concept:C0449560,
umls-concept:C0681873,
umls-concept:C1170232,
umls-concept:C1456409,
umls-concept:C1533691,
umls-concept:C1537432,
umls-concept:C1709595,
umls-concept:C1842480,
umls-concept:C2349200
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pubmed:issue |
6
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pubmed:dateCreated |
2010-6-21
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pubmed:databankReference | |
pubmed:abstractText |
Etravirine (ETR) has previously shown potent in vitro activity against different primary HIV-1 isolates and demonstrated durable efficacy in treatment-experienced, HIV-1-infected patients in the Phase III DUET studies. The antiviral activity and efficacy of ETR against HIV-1 subtypes B and non-B were further investigated. The effect of HIV-1 subtype on ETR fold change in EC(50) value (FC) was analyzed in HIV-1 recombinant clinical isolates from 673 treatment-naive patients enrolled in other Tibotec studies. Subgroup analyses from the DUET studies of the effect of HIV-1 subtype on the proportion of patients with viral load (VL) <50 HIV-1 RNA copies/ml were also conducted using pooled week 48 data. Genotype/subtype and phenotype determinations were performed using the vircoTYPE HIV-1 and Antivirogram assays, respectively. In vitro results from treatment-naive patients indicated comparable median ETR FC in virus isolates from patients infected with subtype B or non-B (1.1 vs. 1.2, respectively). HIV-1 subtype data were available for 594 and 595 patients in the ETR and placebo groups of the DUET studies, respectively; 94% of patients harbored subtype B. Baseline characteristics were similar across the different subtypes, with the exception of a higher number of sensitive NRTIs used in patients with subtype non-B. At week 48, virological responses in the ETR group were higher in patients with subtype non-B versus B (73% vs. 60%, respectively). ETR was equally effective in suppressing viral replication in patients infected with HIV-1 subtype B or various HIV-1 non-B subtypes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1931-8405
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pubmed:author |
pubmed-author:AzijnHildeH,
pubmed-author:De MeyerSandraS,
pubmed-author:De SmedtGoedeleG,
pubmed-author:DierynckIngeI,
pubmed-author:NijsStevenS,
pubmed-author:PicchioGastonG,
pubmed-author:RimskyLaurenceL,
pubmed-author:TambuyzerLotkeL,
pubmed-author:VingerhoetsJohanJ,
pubmed-author:de BéthuneMarie-PierreMP
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pubmed:issnType |
Electronic
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
621-4
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pubmed:meshHeading |
pubmed-meshheading:20507207-Anti-HIV Agents,
pubmed-meshheading:20507207-Genotype,
pubmed-meshheading:20507207-HIV Infections,
pubmed-meshheading:20507207-HIV-1,
pubmed-meshheading:20507207-Humans,
pubmed-meshheading:20507207-Microbial Sensitivity Tests,
pubmed-meshheading:20507207-Phenotype,
pubmed-meshheading:20507207-Pyridazines,
pubmed-meshheading:20507207-RNA, Viral,
pubmed-meshheading:20507207-Treatment Outcome,
pubmed-meshheading:20507207-Viral Load
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pubmed:year |
2010
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pubmed:articleTitle |
Short communication: activity of etravirine on different HIV type 1 subtypes: in vitro susceptibility in treatment-naive patients and week 48 pooled DUET study data.
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pubmed:affiliation |
Tibotec BVBA, Mechelen, Belgium. jvingerh@its.jnj.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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