Comparison of four-drug regimens and pairs of sequential three-drug regimens as initial therapy for HIV-1 infection

被引:184
作者
Shafer, RW
Smeaton, LM
Robbins, GK
De Gruttola, V
Snyder, SW
D'Aquila, RT
Johnson, VA
Morse, GD
Nokta, MA
Martinez, AI
Gripshover, BM
Kaul, P
Haubrich, R
Swingle, M
McCarty, SD
Vella, S
Hirsch, MS
Merigan, TC
Fischl, M
Pollard, R
Dubé, M
Pettinelli, C
Delapenha, R
Putnam, B
Klebert, M
Testa, M
Chiesi, A
Tomino, C
Deeks, S
Nevin, T
Levin, J
French, V
Fennell, O
Stevens, M
Grosso, R
Dusak, B
Hodder, S
Tolson, J
Brothers, C
Leavitt, R
Manion, D
Ruiz, N
Morrisey, K
Becker, M
Quart, B
Jennings, C
Gedeon, L
Dascomb, S
Cooper, M
Murphy, M
机构
[1] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Social & Sci Syst, Silver Spring, MD USA
[5] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[6] Birmingham Vet Affairs Med Ctr, Birmingham, AL USA
[7] Univ Alabama Birmingham, Sch Med, Birmingham, AL USA
[8] SUNY Buffalo, Buffalo, NY 14260 USA
[9] Univ Texas, Med Branch, Galveston, TX 77550 USA
[10] NIAID, Div Aids, NIH, Bethesda, MD 20892 USA
[11] Case Western Reserve Univ, Cleveland, OH 44106 USA
[12] Univ Cincinnati, Coll Med, Cincinnati, OH USA
[13] Univ Calif San Diego, San Diego, CA 92103 USA
[14] Bristol Myers Squibb Co, Plainsboro, NJ USA
[15] GlaxoSmithKline, Res Triangle Pk, NC USA
[16] Ist Super Sanita, I-00161 Rome, Italy
关键词
ACTIVE ANTIRETROVIRAL THERAPY; VIROLOGICAL FAILURE; CLINICAL-TRIALS; NUCLEOSIDE; RESISTANCE; ZIDOVUDINE; LAMIVUDINE; EFAVIRENZ; ADHERENCE; TOXICITY;
D O I
10.1056/NEJMoa030265
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: It is unclear whether therapy for human immunodeficiency virus type 1 (HIV-1) should be initiated with a four-drug or two sequential three-drug regimens. METHODS: In this multicenter trial we compared initial therapy involving four-drug regimens containing efavirenz and nelfinavir in combination with either didanosine and stavudine or zidovudine and lamivudine with therapy involving two consecutive three-drug regimens the first of which contained either efavirenz or nelfinavir. RESULTS: A total of 980 subjects were followed for a median of 2.3 years. There was no significant difference in the occurrence of regimen failures between the group that received the four-drug regimen containing didanosine, stavudine, nelfinavir, and efavirenz and the groups that received the three-drug regimens beginning with didanosine, stavudine, and nelfinavir (hazard ratio for regimen failure, 1.24) or didanosine, stavudine, and efavirenz (hazard ratio, 1.01). There was no significant difference between the group that received the four-drug regimen containing zidovudine, lamivudine, nelfinavir, and efavirenz and the groups that received the three-drug regimens beginning with zidovudine, lamivudine, and nelfinavir (hazard ratio, 1.06) or zidovudine, lamivudine, and efavirenz (hazard ratio, 1.45). A four-drug regimen was associated with a longer time to the first regimen failure than the three-drug regimens containing didanosine, stavudine, and nelfinavir (hazard ratio for a first regimen failure, 0.55); didanosine, stavudine, and efavirenz (hazard ratio, 0.63); or zidovudine, lamivudine, and nelfinavir (hazard ratio, 0.49), but not the three-drug regimen containing zidovudine, lamivudine, and efavirenz (hazard ratio, 1.21). CONCLUSIONS: There was no significant difference in the duration of successful HIV-1 treatment between a single four-drug regimen and two consecutive three-drug regimens. Among these treatment strategies, initiating therapy with the three-drug regimen of zidovudine, lamivudine, and efavirenz is the optimal choice.
引用
收藏
页码:2304 / 2315
页数:12
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