Which antiretrovirals should be prescribed as first-line treatments? Changes over the past 10 years in France

被引:1
|
作者
Pugliese, P. [1 ]
Joly, V [2 ,3 ]
Valantin, M. A. [4 ]
Cotte, L. [5 ]
Huleux, T. [6 ]
Allavena, C. [7 ]
Reynes, J. [8 ]
Poizot-Martin, I [9 ,10 ]
Bani-Sadr, F. [11 ]
Cuzin, L. [12 ,13 ,14 ]
Bregigeon, S.
Faucher, O.
Orticoni, M.
Soavi, M. J.
de Lamarliere, P. Geneau
Laroche, H.
Ressiot, E.
Carta, M.
Ducassou, M. J.
Jacquet, I
Gallie, S.
Galinier, A.
Ritleng, A. S.
Ivanova, A.
Blanco-Betancourt, C.
Lions, C.
Debreux, C.
Obry-Roguet, V
Alvarez, M.
Biezunski, N.
Debard, A.
Delobel, P.
Delpierre, C.
Garipuy, D.
Lansalot, P.
Lelievre, L.
Lepain, I
Marcel, M.
Marchou, B.
Martin-Blondel, G.
Metsu, D.
Mularczyk, M.
Porte, L.
Puntis, E.
Saune, K.
Ceppi, C.
Cua, E.
Cottalorda, J.
Dellamonica, P.
Demonchy, E.
机构
[1] Hop Archet, Malad Infect, F-06000 Nice, France
[2] Hop Bichat Claude Bernard, Malad Infect & Trop, F-75877 Paris, France
[3] Univ Paris Diderot, INSERM, IAME, UMR 1137, F-75877 Paris, France
[4] Hop La Pitie Salpetriere, Malad Infect, F-75013 Paris, France
[5] CHU Lyon, Malad Infect, F-69002 Lyon, France
[6] CH Tourcoing, Malad Infect, F-59200 Tourcoing, France
[7] CHU Hotel Dieu, Malad Infect, F-42000 Nantes, France
[8] CHU Montpellier, Malad Infect, IRD UMI233, Inserm U1175, F-34000 Montpellier, France
[9] Univ Aix Marseille, Hop St Marguerite, AP HM, Serv Immunohematol, F-13009 Marseille, France
[10] 2 Inserm U912 SESSTIM, F-13009 Marseille, France
[11] Univ Reims, Fac Med, Hop Robert Debre, EA SFR CAP Sante Malad Infect & Trop 4684,CHU Rei, F-51100 Reims, France
[12] INSERM, UMR 1027, F-31000 Toulouse, France
[13] Univ Toulouse III, F-31000 Toulouse, France
[14] CHU Toulouse, COREVIH Toulouse, F-31000 Toulouse, France
来源
MEDECINE ET MALADIES INFECTIEUSES | 2019年 / 49卷 / 04期
关键词
Initial HIV therapy; Integrase strand transfer inhibitors; HIV infection; CO-FORMULATED ELVITEGRAVIR; ONCE-DAILY DOLUTEGRAVIR; HIV-1; INFECTION; DOUBLE-BLIND; INITIAL TREATMENT; NAIVE PATIENTS; EMTRICITABINE; RALTEGRAVIR; COBICISTAT; TENOFOVIR;
D O I
10.1016/j.medmal.2018.10.005
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objective. - To describe the changes in first-line antiretroviral (ART) regimens in France between 2005 and 2015 and patients' characteristics related to the use of protease inhibitors in 2015. Methods. - We extracted all patients starting ART between 2005 and 2015 from a large prospective cohort. Regimens were classified as three nucleoside reverse transcriptase inhibitors (NRTI), or two NRTIs with a boosted protease inhibitor (bPI), with a non-nucleoside reverse transcriptase inhibitor (NNRTI), or with an INSTI. Patients' characteristics at the time of initiation were collected. A multinomial logit model was fitted to analyze characteristics related to the choice of regimen in 2015. Results. - We analyzed data from 15,897 patients. The proportion of patients starting with (i) a bPI decreased from 60% before 2014 to 38.1% in 2015; (ii) an NNRTI decreased from 30% to 17.8% in 2015; (iii) an INSTI gradually increased to 39.4% in 2015. In 2015, patients with an initial viral load >5 log copies/mL were less likely to receive NNRTI (OR = 0.08) or INSTI regimens (OR = 0.69) than bPIs. Patients with initial CD4(+) T cell count <200/mm(3) were less likely to receive an NNRTI (OR = 0.28) or an INSTI regimen (OR = 0.52) than a bPI. Women were less likely to receive an NNRTI (OR = 0.79) or an INSTI regimen (OR = 0.71) than a bPI; although this depended on age. Conclusion. - The use of bPI as first-line ART declined sharply in France from 2005 to 2015. bPI remained of preferential use in patients with high viral load, low CD4(+) T cell count, and in women. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:264 / 269
页数:6
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