Compact quadruple therapy with the lamivudine/zidovudine combination tablet plus abacavir and efavirenz, followed by the lamivudine/zidovudine/abacavir triple nucleoside tablet plus efavirenz in treatment-naive HIV-infected adults

被引:0
|
作者
Ruane, PJ
Parenti, DM
Margolis, DM
Shepp, DH
Babinchak, TJ
van Kempen, AS
Kauf, TL
Danehower, SA
Yau, L
Hessenthaler, SM
Goodwin, SD
Hernandez, JE
机构
[1] Tower ID Med Associates Inc, Los Angeles, CA 90049 USA
[2] George Washington Univ, Ctr Med, Washington, DC USA
[3] Univ Texas, SW Med Ctr, Dallas, TX USA
[4] NYU, Dept Med, Jane & Dayton Brown & Dayton T Brown Jr Virol La, N Shore Univ Hosp,Sch Med, Manhasset, NY USA
[5] Thomas Jefferson Univ, Dorrance H Hamilton Labs, Ctr Human Virol, Div Infect Dis,Dept Med,Jefferson Med Coll, Philadelphia, PA 19107 USA
[6] GlaxoSmithKline, Res Triangle Pk, NC USA
来源
HIV CLINICAL TRIALS | 2003年 / 4卷 / 04期
关键词
abacavir; adherence; Combivir; efavirenz; HIV infection; immune reconstitution; quadruple combination antiretroviral therapy; Trizivir;
D O I
暂无
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose: To assess efficacy, safety, and adherence with compact quadruple therapy comprising one lamivudine 150-mg/zidovudine 300-mg tablet (COM) twice daily + one abacavir (ABC) 300-mg tablet twice daily + three efavirenz (EFV) 200-mg capsules at bedtime for 24 weeks, followed by one lamivudine 150-mg/zidovudine 300-mg/ ABC 300-mg triple nucleoside tablet (TZV) twice daily + three EFV 200-mg capsules at bedtime for 24 weeks. Method: A pilot 48-week, prospective, open-label trial in which 38 antiretroviral naive HIV-infected adults (baseline median HIV-1 RNA 5.1 log(10) copies/mL, CD4+ cell count 285/muL) received the above treatment and were monitored regularly with respect to plasma HIV-1 RNA levels, CD4+ cell counts, T-cell receptor excision circles (TRECs), adherence, and adverse events. Results: At Week 48, intent-to-treat, switch-included analysis showed plasma HIV-1 RNA levels <400 copies/mL in 100% (29/29) of patients and <50 copies/mL in 93% (27/29); 59% of patients who achieved <50 copies/mL had &LT;3 copies/mL (16/27). Similar virologic suppression was observed in patients with baseline HIV-1 RNA above or below 100,000 copies/mL. HIV-1 RNA and CD4+ cell counts changed from baseline by a median of -3.4 log,, copies/mL and +172 cells/μL, respectively. One virologic failure occurred at Week 16. Median TRECs/100,000 peripheral blood lymphocytes increased 6-fold between baseline and Week 48. Median adherence rates were consistently 100% by self-report and 94% by pill count. Grade 2-4 treatment-related adverse events included dreams (16%), nausea (13%), decreased white cells (8%), dizziness (8%), sleep disorders (8%), and malaise and fatigue (8%). A suspected ABC hypersensitivity reaction occurred in 8% (3/38) of patients. Conclusion: COM/ABC/ EFV or TZV/EFV produced potent, durable virologic suppression and immunologic benefits, was associated with high adherence rates, and was generally well tolerated.
引用
收藏
页码:231 / 243
页数:13
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