Darunavir: A Review of Its Use in the Management of HIV-1 Infection

被引:70
作者
Deeks, Emma D. [1 ]
机构
[1] Adis, Auckland 0754, New Zealand
关键词
TREATMENT-EXPERIENCED PATIENTS; ONCE-DAILY DARUNAVIR/RITONAVIR; NAIVE HIV-1-INFECTED PATIENTS; RESISTANCE-ASSOCIATED MUTATIONS; LOW-DOSE RITONAVIR; TWICE-DAILY DARUNAVIR/RITONAVIR; PROTEASE INHIBITOR-RESISTANT; COST-EFFECTIVENESS; VIROLOGICAL RESPONSE; ANTIRETROVIRAL THERAPY;
D O I
10.1007/s40265-013-0159-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The latest HIV-1 protease inhibitor (PI) darunavir (Prezista (TM)) has a high genetic barrier to resistance development and is active against wild-type HIV and HIV strains no longer susceptible to some older PIs. Ritonavir-boosted darunavir, as a component of antiretroviral therapy (ART), is indicated for the treatment of HIV-1 infection in adult and paediatric patients (aged >= 3 years), with or without treatment experience (details vary depending on region of approval). Several open-label or partially-blinded trials have evaluated the efficacy of ritonavir-boosted darunavir ART regimens for up to 192 weeks in these settings. In treatment-na < ve adults, once-daily boosted darunavir was no less effective in establishing virological suppression than once- or twice-daily boosted lopinavir, yet was more effective at maintaining suppression long term. Moreover, treatment-experienced adults with no darunavir resistance-associated mutations (RAMs) had no less effective viral load suppression with once-daily than with twice-daily boosted darunavir. In treatment-experienced adults, including some with multiple major PI RAMs, twice-daily boosted darunavir was more effective than twice-daily boosted lopinavir or boosted control PIs in reducing viral load, and provided virological benefit as part of a salvage regimen in those with few remaining treatment options. Boosted darunavir also reduced viral load when administered once-daily in treatment-na < ve adolescents or twice-daily in treatment-experienced children and adolescents. Boosted darunavir is generally well tolerated, with gastrointestinal disturbances and lipid abnormalities among the most common tolerability issues. It has a lipid profile more favourable than that of boosted lopinavir in terms of total cholesterol and triglyceride changes and, when administered once daily, its lipid effects are generally similar to those of boosted atazanavir. Thus, boosted darunavir is a useful option for the ART regimens of adult and paediatric patients with HIV-1 infection.
引用
收藏
页码:99 / 125
页数:27
相关论文
共 113 条
[1]   Metabolic Effects of Darunavir/Ritonavir Versus Atazanavir/Ritonavir in Treatment-Naive, HIV Type 1-Infected Subjects over 48 Weeks [J].
Aberg, Judith A. ;
Tebas, Pablo ;
Overton, Edgar Turner ;
Gupta, Samir K. ;
Sax, Paul E. ;
Landay, Alan ;
Falcon, Ron ;
Ryan, Robert ;
De La Rosa, Guy .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2012, 28 (10) :1184-1195
[2]  
AIDS.GOV, 2013, GLOB HIV AIDS CRIS T
[3]   Lessons from a multicentre paediatric HIV trial [J].
Ananworanich, Jintanat ;
Puthanakit, Thanyawee ;
Saphonn, Vonthanak ;
Cooper, David A. ;
Ruxrungtham, Kiat .
LANCET, 2008, 372 (9636) :356-357
[4]  
[Anonymous], 19 C RETR OPP INF 5
[5]  
[Anonymous], 2013, Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents
[6]  
[Anonymous], GUID VERS 7 0
[7]  
[Anonymous], 2011, HIV drug resistance fact sheet
[8]  
Antoniou Tony, 2010, J Int Assoc Physicians AIDS Care (Chic), V9, P382, DOI 10.1177/1545109710382041
[9]   Efficacy and safety of darunavir/ritonavir in treatment-experienced HIV type-1 patients in the POWER 1, 2 and 3 trials at week 96 [J].
Arasteh, Keikawus ;
Yeni, Patrick ;
Pozniak, Anton ;
Grinsztejn, Beatriz ;
Jayaweera, Dushyantha ;
Roberts, Afsoon ;
Hoy, Jennifer ;
De Meyer, Sandra ;
Vangeneugden, Tony ;
Tomaka, Frank .
ANTIVIRAL THERAPY, 2009, 14 (06) :859-864
[10]   Effects of once-daily darunavir/ritonavir versus lopinavir/ritonavir on metabolic parameters in treatment-naive HIV-1-infected patients at week 96: ARTEMIS [J].
Arathoon, E. ;
Schneider, S. ;
Baraldi, E. ;
Lim, P. L. ;
Opravil, M. ;
Van De Casteele, T. ;
Lavreys, L. .
INTERNATIONAL JOURNAL OF STD & AIDS, 2013, 24 (01) :12-17