首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >A randomized comparative trial of stavudine (d4T) versus zidovudine (ZDV, AZT) in children with human immunodeficiency virus infection. AIDS Clinical Trials Group 240 Team.
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A randomized comparative trial of stavudine (d4T) versus zidovudine (ZDV, AZT) in children with human immunodeficiency virus infection. AIDS Clinical Trials Group 240 Team.

机译:司他夫定(d4T)与齐多夫定(ZDV,AZT)在人类免疫缺陷病毒感染儿童中的随机对照试验。艾滋病临床试验小组240组。

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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/m2 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/microL (range, 18 to 4238 cells/microL). Neutropenia < 400/microL 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.
机译:目的:比较司他夫定(d4T)与齐多夫定(ZDV,AZT)在有症状的3个月至6岁的人类免疫缺陷病毒感染儿童中的安全性和耐受性。方法:在最初的双盲试验中,将接受不超过6周先前抗逆转录病毒治疗的212例可评估的人类免疫缺陷病毒感染儿童随机分配为接受d4T(每12小时口服1 mg / kg,最多40 mg口服)每12小时一次)或齐多夫定(每6小时口服180 mg / m2,每6小时最大口服200 mg)。中位随访6.3个月后,该研究无盲。研究结束时的中位随访时间为17.3个月。评估耐受性,安全性,疾病进展和免疫应答。结果:该患者人群为年轻(中位年龄1.2岁;范围0.3至6.4岁),基线CD4 +淋巴细胞中位数为965个细胞/微升(范围18至4238个细胞/微升)。与接受d4T的儿童(1年事件发生率5%至5%)相比,齐多夫定接受者中的中性粒细胞减少症<400 / microL发生率更高(直到解盲时和整个研究期间的1年事件发生率均为20%)。解盲时间和整个研究的6%)。在使用收集到研究结束之前收集到的所有数据进行的探索性活动分析中,接受d4T治疗的儿童在年龄和性别上的体重z得分均较基线表现出了更大的积极变化。如预期的那样,这两个治疗组的中位数绝对CD4 +淋巴细胞计数均下降。在d4T接受者中,基线的变化较小。结论:在3个月至6岁的儿童中,d4T和齐多夫定在安全性和耐受性方面具有相当的可比性。在接受d4T治疗的儿童中,中性粒细胞减少症的发生率明显降低。有证据表明接受d4T的儿童体重增加和CD4 +绝对淋巴细胞计数得到更好的维持。

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