Efavirenz - Still first-line king?

被引:30
作者
Best, Brookie M. [1 ,2 ]
Goicoechea, Miguel [3 ]
机构
[1] Univ Calif San Diego, Sch Med, Dept Pediat, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Div Pharmacol & Drug Discovery, San Diego, CA 92103 USA
[3] Antiviral Res Ctr, San Diego, CA 92103 USA
关键词
efavirenz; treatment naive; novel antiretroviral agents;
D O I
10.1517/17425255.4.7.965
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Efavirenz is a potent, safe and tolerable non-nucleoside reverse transcriptase inhibitor (NNRTI) recommended as initial therapy. Recently, several new antiretroviral drugs, including second generation NNRTIs, protease-inhibitors, an integrase-inhibitor and a CCR5 inhibitor, have become or will be shortly available. Objective: This article will review relevant efficacy and safety data of efavirenz compared to these novel agents or certain common alternate drugs currently used as initial therapy in treatment-naive patients. Methods: Published articles and conference presentations pertaining to efavirenz and/or the newer antiretroviral agents were evaluated. Results/conclusions: Efavirenz will continue to be preferred initial therapy for now. if longer-term studies of integrase inhibitors and second-generation NNRTIs confirm initial findings, they will eventually supplant efavirenz as preferred first-line agents.
引用
收藏
页码:965 / 972
页数:8
相关论文
共 48 条
[1]   Nelfinavir, efavirenz, or both after the failure of nucleoside treatment of HIV infection. [J].
Albrecht, MA ;
Bosch, RJ ;
Hammer, SM ;
Liou, SH ;
Kessler, H ;
Para, MF ;
Eron, J ;
Valdez, H ;
Dehlinger, M ;
Katzenstein, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (06) :398-407
[2]  
[Anonymous], GUID US ANT AG HIV 1
[3]   Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy [J].
Bacheler, LT ;
Anton, ED ;
Kudish, P ;
Baker, D ;
Bunville, J ;
Krakowski, K ;
Bolling, L ;
Aujay, M ;
Wang, XV ;
Ellis, D ;
Becker, MF ;
Lasut, AL ;
George, HJ ;
Spalding, DR ;
Hollis, G ;
Abremski, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) :2475-2484
[4]   Long-term results of initial therapy with abacavir and lamivudine combined with efavirenz, amprenavir/ritonavir, or stavudine [J].
Bartlett, John A. ;
Johnson, Judy ;
Herrera, Gisela ;
Sosa, Nestor ;
Rodriguez, Alan ;
Liao, Qiming ;
Griffith, Sandy ;
Irlbeck, David ;
Shaefer, Mark S. .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2006, 43 (03) :284-292
[5]  
*BM SQUIB CO, 2008, SUSTIVA PRESCR INF
[6]   A V106M mutation in HIV-1 clade C viruses exposed to efavirenz confers cross-resistance to non-nucleoside reverse transcriptase inhibitors [J].
Brenner, B ;
Turner, D ;
Oliveira, M ;
Moisi, D ;
Detorio, M ;
Carobene, M ;
Marlink, RG ;
Schapiro, J ;
Roger, M ;
Wainberg, MA .
AIDS, 2003, 17 (01) :F1-F5
[7]   Efavirenz use during pregnancy and for women of child-bearing potential [J].
Chersich M.F. ;
Urban M.F. ;
Venter F.W.D. ;
Wessels T. ;
Krause A. ;
Gray G.E. ;
Luchters S. ;
Viljoen D.L. .
AIDS Research and Therapy, 3 (1)
[8]   Reverse transcriptase mutations 118I, 208Y, and 215Y cause HIV-1 hypersusceptibility to non-nucleoside reverse transcriptase inhibitors [J].
Clark, Shauna A. ;
Shulman, Nancy S. ;
Bosch, Ronald J. ;
Mellors, John W. .
AIDS, 2006, 20 (07) :981-984
[9]   Impact of efavirenz on neuropsychological performance and symptoms in HIV-infected individuals [J].
Clifford, DB ;
Evans, S ;
Yang, YJ ;
Acosta, EP ;
Goodkin, K ;
Tashima, K ;
Simpson, D ;
Dorfman, D ;
Ribaudo, H ;
Gulick, RM .
ANNALS OF INTERNAL MEDICINE, 2005, 143 (10) :714-721
[10]  
CLUMECK NVJ, 2007, EUR AIDS C OCT 24 27