Nevirapine versus atazanavir/ritonavir, each combined with tenofovir disoproxil fumarate/emtricitabine, in antiretroviral-naive HIV-1 patients: the ARTEN Trial

被引:77
作者
Soriano, Vicente [1 ]
Arasteh, Keikawus [2 ]
Migrone, Horacio [3 ]
Lutz, Thomas [4 ]
Opravil, Milos [5 ]
Andrade-Villanueva, Jaime [6 ]
Antunes, Francisco [7 ]
Di Perri, Giovanni [8 ]
Podzamczer, Daniel [9 ]
Taylor, Steve [10 ]
Domingo, Pere [11 ]
Gellermann, Holger [12 ]
de Rossi, Lothar [12 ]
机构
[1] Hosp Carlos III, Dept Infect Dis, Madrid, Spain
[2] Epimed GmbH, Berlin, Germany
[3] Infectol Asistencia Ambulatoria, Buenos Aires, DF, Argentina
[4] Infektiologicum Frankfurt, Frankfurt, Germany
[5] Univ Zurich Hosp, Dept Internal Med, Zurich, Switzerland
[6] Antiguo Hosp Civil, Guadalajara, Jalisco, Mexico
[7] Hosp Santa Maria, Serv Doencas Infecciosas, Lisbon, Portugal
[8] Univ Turin, Dept Infect Dis, Turin, Italy
[9] Hosp Univ Bellvitge, Infect Dis Serv, Barcelona, Spain
[10] Birmingham Heartlands Hosp, Directorate Infect, Birmingham B9 5ST, W Midlands, England
[11] Hosp Santa Creu & Sant Pau, HIV Unit, Barcelona, Spain
[12] Boehringer Ingelheim GmbH & Co KG, Ingelheim, Germany
关键词
EARLY VIROLOGICAL FAILURE; APOLIPOPROTEIN-A-I; INFECTED PATIENTS; HIV-1-INFECTED PATIENTS; MYOCARDIAL-INFARCTION; PROTEASE INHIBITORS; REGIMEN SIMPLIFICATION; CLINICAL-TRIALS; THERAPY; SAFETY;
D O I
10.3851/IMP1745
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Selection of first-line antiretroviral therapy requires consideration of efficacy as well as effects on lipids given the increased concern about cardiovascular risk in HIV-1 patients. Methods: ARTEN is a randomized, open-label, non-inferiority trial that compares nevirapine (NVP) 200 mg twice daily or 400 mg once daily to atazanavir/ritonavir (ATZ/r) 300 mg/100 mg once daily, each combined with fixed-dose tenofovir disoproxil fumarate (TDF) 300 mg/emtricitabine (FTC) 200 mg once daily, in antiretroviralnaive HIV-1 patients with CD4(+) T-cell counts <400 (men) and <250 cells/mm(3) (women). The primary end point was plasma HIV RNA<50 copies/ml at two consecutive visits prior to week 48. Results: A total of 569 patients were randomized and treated. Overall, 66.8% of NVP and 65.3% of ATZ/r patients achieved the primary end point (difference 1.9%, 95% Cl -5.9-9.8%). Similar rates of serious adverse events were observed (9.6% on NVP versus 8.8% on ATZ/r), although discontinuations due to adverse events were more frequent with NVP than ATZ/r (13.6% versus 3.6%, respectively). None of the 28 patients virologically failing ATZ/r selected resistance mutations, while they were selected in 29/44 patients virologically failing NVP. NVP induced a significantly greater increase in high-density lipoprotein cholesterol (HDL-c) and apolipoprotcin A1 from baseline than ATZ/r, whereas triglycerides increased significantly more with ATZ/r than NVP. Mean change from baseline in TC:HDL-c ratio was -0.24 for NVP and 0.13 for ATZ/r (P=0.0001). Conclusions: NVP demonstrated at week 48 non-inferior antiviral efficacy compared with ATZ/r when given along with TDF/FTC, despite more drug-related discontinuations with NVP than ATZ/r. NVP was associated with a lower atherogenic lipid profile than ATZ/r although resistance mutations were more frequently selected with NVP than ATZ/r.
引用
收藏
页码:339 / 348
页数:10
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