A randomized comparative trial of stavudine (d4T) versus zidovudine (ZDV, AZT) in children with human immunodeficiency virus infection

被引:35
作者
Kline, MW
Van Dyke, RB
Lindsey, JC
Gwynne, M
Culnane, M
McKinney, RE
Nichols, S
Mitchell, WG
Yogev, R
Hutcheon, N
机构
[1] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Houston, TX 77030 USA
[3] Tulane Univ, Sch Med, Dept Pediat, New Orleans, LA 70112 USA
[4] Harvard Univ, Sch Publ Hlth, Ctr Biostat AIDS Res, Boston, MA 02115 USA
[5] Pediat ACTG Operat Ctr, Rockville, MD USA
[6] NIAID, Div Aids, Bethesda, MD 20892 USA
[7] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
[8] Univ Calif San Diego, Sch Med, Dept Neurosci, San Diego, CA 92103 USA
[9] Childrens Hosp Los Angeles, Dept Pediat, Los Angeles, CA 90027 USA
[10] Univ So Calif, Sch Med, Los Angeles, CA USA
[11] Childrens Mem Hosp, Dept Pediat, Chicago, IL 60614 USA
[12] Northwestern Univ, Sch Med, Chicago, IL USA
[13] St Josephs Hosp & Med Ctr, Dept Pediat, Newark, NJ USA
关键词
stavudine; zidovudine; HIV infection; infant or child;
D O I
10.1542/peds.101.2.214
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives. To compare the safety and tolerance of stavudine (d4T) versus zidovudine (ZDV, AZT) in symptomatic human immunodeficiency virus-infected children 3 months to 6 years of age. Methods. In an initially double-blind trial, 212 evaluable human immunodeficiency virus-infected children who had received no more than 6 weeks of previous antiretroviral therapy were randomized to receive either d4T (1 mg/kg orally every 12 hours, maximum 40 mg orally every 12 hours) or zidovudine (180 mg/m(2) orally every 6 hours, maximum 200 mg orally every 6 hours). The study was unblinded after a median follow-up period of 6.3 months; median follow-up at study closure was 17.3 months. Tolerance, safety, disease progression, and immunologic responses were evaluated. Results. The patient population was young (median age, 1.2 years; range, 0.3 to 6.4 years), with a median baseline CD4+ lymphocyte count of 965 cells/mu L (range, 18 to 4238 cells/mu L). Neutropenia <400/mu L occurred significantly more commonly among zidovudine recipients (1-year event rates of 20% both up to the time of unblinding and throughout the entire study) than among children receiving d4T (1-year event rates of 5% up to the time of unblinding and 6% throughout the entire study). In exploratory activity analyses using all data collected until study closure, children treated with d4T showed consistently greater positive changes from baseline in weight-for-age-and-gender z scores. As expected in this population of young children, median absolute CD4+ lymphocyte counts decreased in both treatment groups. Smaller changes from baseline were noted among d4T recipients. Conclusions. In children between the ages of 3 months and 6 years, d4T and zidovudine are largely comparable in terms of safety and tolerance. Neutropenia occurs significantly less commonly among children treated with d4T. There was evidence that weight gain and absolute CD4+ lymphocyte counts were better maintained in children receiving d4T.
引用
收藏
页码:214 / 220
页数:7
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