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Co-administration of elvitegravir/cobicistat/tenofovir disoproxil fumarate/emtricitabine and atazanavir in treatment-experienced HIV patients
被引:0
|作者:
Biagi, M.
[1
]
Badowski, M. E.
[1
]
Chiampas, T.
[1
]
Young, J.
[2
]
Patel, M.
[2
]
Vaughn, P.
[3
]
机构:
[1] Univ Illinois, Coll Pharm, Dept Pharm Practice, 1940 W,Taylor St,Room 312, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Med, Infect Dis Sect, Chicago, IL USA
[3] Univ Illinois, Dept Med, Chicago, IL USA
关键词:
Treatment-experienced;
antiretroviral therapy;
antiretroviral resistance;
HIV;
AIDS;
elvitegravir;
cobicistat;
emtricitabine;
tenofovir;
atazanavir;
ACUTE INTERSTITIAL NEPHRITIS;
RENAL-FAILURE;
PROTEASE INHIBITOR;
TENOFOVIR;
COBICISTAT;
THERAPY;
PHARMACOENHANCER;
METAANALYSIS;
RITONAVIR;
INFECTION;
D O I:
10.1177/0956462416666440
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
We report the use of elvitegravir 150mg/cobicistat 150mg/tenofovir disoproxil fumarate 300mg/emtricitabine 200mg (EVG/COBI/TDF/FTC) once daily, in addition to once-daily atazanavir (ATV) 300mg, in treatment-experienced patients with human immunodeficiency virus (HIV). Due to limited data available on the co-administration of these agents, our objective was to evaluate and monitor safety and efficacy of this regimen in patients who developed resistance or intolerance to conventional antiretroviral therapy (ART). This short report included offenders incarcerated in the Illinois Department of Corrections who were 18 years, HIV-infected, had documented antiretroviral resistance, and received EVG/COBI/TDF/FTC+ATV once daily. Based on previous ART, resistance patterns and current medications, seven patients were initiated on once-daily therapy consisting of EVG/COBI/TDF/FTC and ATV. Due to extensive resistance, two of the seven patients were also started on abacavir (ABC) 600mg daily in addition to EVG/COBI/TDF/FTC and ATV. Of the seven patients, one had ART changed due to concerns of resistance based on a genotype, one experienced a decline in renal function that warranted a change in therapy, and one is currently virologically suppressed on a combination of EVG/COBI/TDF/FTC, ATV, and ABC. The remaining four patients remain virologically suppressed on EVG/COBI/TDF/FTC+ATV. Therapy consisting of EVG/COBI/TDF/FTC and ATV may be a viable option for some treatment-experienced HIV-infected patients. Further studies evaluating the safety, efficacy, and pharmacokinetics of this therapy are warranted, given the lack of information currently available.
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页码:766 / 772
页数:7
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