Efficacy of a nucleoside-sparing regimen of darunavir/ritonavir plus raltegravir in treatment-naive HIV-1-infected patients (ACTG A5262)

被引:119
作者
Taiwo, Babafemi [1 ]
Zheng, Lu [2 ]
Gallien, Sebastien [3 ]
Matining, Roy M. [2 ]
Kuritzkes, Daniel R. [3 ]
Wilson, Cara C. [4 ]
Berzins, Baiba I. [1 ]
Acosta, Edward P. [5 ]
Bastow, Barbara [7 ]
Kim, Peter S. [6 ]
Eron, Joseph J., Jr. [8 ]
机构
[1] Northwestern Univ, Div Infect Dis, Chicago, IL 60611 USA
[2] Harvard Univ, Sch Publ Hlth, Stat Data Anal Ctr, Boston, MA 02115 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Sect Retroviral Therapeut, Boston, MA 02115 USA
[4] Univ Colorado, Hlth Sci Ctr, Div Infect Dis, Denver, CO USA
[5] Univ Alabama Birmingham, Div Clin Pharmacol, Dept Pharmacol & Toxicol, Birmingham, AL 35294 USA
[6] NIAID, Div Aids, NIH, Bethesda, MD 20892 USA
[7] Social & Sci Syst Inc, ACTG Operat Ctr, Silver Spring, MD USA
[8] Univ N Carolina, Div Infect Dis, Chapel Hill, NC USA
关键词
antiretroviral therapy; darunavir; nucleoside sparing; raltegravir; ANTIRETROVIRAL DRUG-RESISTANCE; ONCE-DAILY DARUNAVIR/RITONAVIR; HIV-1 VIRAL LOAD; INITIAL TREATMENT; LOPINAVIR/RITONAVIR; SAFETY; INFECTION; COMBINATION; TENOFOVIR;
D O I
10.1097/QAD.0b013e32834bbaa9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To explore darunavir/ritonavir (DRV/r) plus raltegravir (RAL) combination therapy in antiretroviral-naive patients. Design: Phase IIb, single-arm, open-label, multicenter study. Methods: One hundred and twelve antiretroviral-naive, HIV-1-infected patients received DRV/r 800/100 mg once daily and RAL 400 mg twice daily. Primary endpoint was virologic failure by week 24. Virologic failure was defined as confirmed viral load of 1000 copies/ml or more at week 12, or an increase of more than 0.5 log(10) copies/ml in viral load from week 4 to 12, or a confirmed viral load of more than 50 copies/ml at or after week 24. Protease and integrase genes were sequenced in patients experiencing virologic failure. Results: Virologic failure rate was 16% [95% confidence interval (CI) 10-24] by week 24 and 26% (95% CI 19-36) by week 48 in an intent-to-treat analysis. Viral load at virologic failure was 51-200 copies/ml in 17/28 failures. Adjusting for age and sex, virologic failure was associated with baseline viral load of more than 100 000 copies/ml [hazard ratio 3.76, 95% CI (1.52-9.31), P = 0.004] and lower CD4 cell count [0.77 per 100 cells/mu l increase (95% CI 0.61-0.98), P - 0.037]. When trough RAL concentrations were included as a time-varying covariate in the analysis, virologic failure remained associated with baseline viral load more than 100 000 copies/ml [hazard ratio = 4.67 (95% CI 1.93-11.25), P < 0.001], whereas RAL level below detection limit in plasma at one or more previous visits was associated with increased hazard [hazard ratio = 3.42 (95% CI 1.41-8.26), P = 0.006]. All five participants with integrase mutations during virologic failure had baseline viral load more than 100 000 copies/ml. Conclusion: DRV/r plus RAL was effective and well tolerated in most patients, but virologic failure and integrase resistance were common, particularly in patients with baseline viral load more than 100 000 copies/ml. (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:2113 / 2122
页数:10
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