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ALBI试验:一项随机对照试验,比较司他夫定加去羟肌苷与齐多夫定加拉米夫定,以及在既往未接受治疗的人类免疫缺陷病毒感染患者中交替使用这两种组合的方案。

The ALBI trial: a randomized controlled trial comparing stavudine plus didanosine with zidovudine plus lamivudine and a regimen alternating both combinations in previously untreated patients infected with human immunodeficiency virus.

作者信息

Molina J M, Chêne G, Ferchal F, Journot V, Pellegrin I, Sombardier M N, Rancinan C, Cotte L, Madelaine I, Debord T, Decazes J M

机构信息

Clinique des Maladies Infectieuses, Hôpital Saint-Louis, 75475 Paris Cedex 10, France.

出版信息

J Infect Dis. 1999 Aug;180(2):351-8. doi: 10.1086/314891.

Abstract

A total of 151 previously untreated patients infected with human immunodeficiency virus type 1 (HIV-1) with CD4 cell counts >/=200/microL and plasma HIV-1 RNA levels of 10,000-100,000 copies/mL were randomly assigned to 24 weeks of open-labeled stavudine plus didanosine (group 1), zidovudine plus lamivudine (group 2), or stavudine plus didanosine followed by zidovudine plus lamivudine (group 3). The mean decrease in HIV-1 RNA level was greater in group 1 (2.26 log10 copies/mL) than in groups 2 (1.26 log10 copies/mL) or 3 (1.58 log10 copies/mL; P<.0001). The mean increase in CD4 cell counts was greater in groups 1 (124 cells/microL) and 3 (118 cells/microL) than in group 2 (62 cells/microL; P=.02). All regimens were generally well tolerated. The combination of stavudine plus didanosine reduced plasma HIV-1 RNA concentrations and increased CD4 cell counts more effectively than did the combination of zidovudine plus lamivudine or the regimen alternating both combinations.

摘要

共有151例既往未接受治疗的1型人类免疫缺陷病毒(HIV-1)感染者,其CD4细胞计数≥200/μL,血浆HIV-1 RNA水平为10,000 - 100,000拷贝/mL,被随机分配接受24周的开放标签司他夫定加去羟肌苷治疗(第1组)、齐多夫定加拉米夫定治疗(第2组)或司他夫定加去羟肌苷治疗后再接受齐多夫定加拉米夫定治疗(第3组)。第1组的HIV-1 RNA水平平均下降幅度(2.26 log10拷贝/mL)大于第2组(1.26 log10拷贝/mL)或第3组(1.58 log10拷贝/mL;P<0.0001)。第1组(124个细胞/μL)和第3组(118个细胞/μL)的CD4细胞计数平均增加幅度大于第2组(62个细胞/μL;P = 0.02)。所有治疗方案总体耐受性良好。与齐多夫定加拉米夫定联合方案或两种联合方案交替使用的方案相比,司他夫定加去羟肌苷联合方案能更有效地降低血浆HIV-1 RNA浓度并增加CD4细胞计数。

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