Browne M J, Mayer K H, Chafee S B, Dudley M N, Posner M R, Steinberg S M, Graham K K, Geletko S M, Zinner S H, Denman S L
Brown University AIDS Program, Providence, RI.
J Infect Dis. 1993 Jan;167(1):21-9. doi: 10.1093/infdis/167.1.21.
2',3'-didehydro-3'-deoxythymidine (d4T) is a pyrimidine analogue and inhibitor of reverse transcriptase with potent in vitro activity against human immunodeficiency virus (HIV). A phase I trial of d4T was conducted in 41 HIV-infected patients, 12 with AIDS and 29 with AIDS-related complex (ARC). Thirty-six patients were evaluatable. The maximum tolerated dose was 2 mg/kg/day. The dose-limiting toxicity was sensory peripheral neuropathy, which occurred in 20 patients (55%). Four patients (11%) developed hepatotoxicity. Five (14%) developed anemia requiring a transfusion but not discontinuation of drug. The mean +/- SE plasma elimination half-life at all dose levels was 1.2 +/- 0.09 h. Increased or stable absolute CD4 counts were seen in most patients. The majority of patients with detectable serum p24 antigen levels had a persistent decrease by 6 months. d4T is a promising drug for patients with AIDS or ARC. This clinical trial is continuing to determine the minimal effective dose.
2',3'-二脱氢-3'-脱氧胸苷(d4T)是一种嘧啶类似物,也是逆转录酶抑制剂,在体外对人类免疫缺陷病毒(HIV)具有强大的活性。对41例HIV感染患者进行了d4T的I期试验,其中12例患有艾滋病,29例患有艾滋病相关综合征(ARC)。36例患者可进行评估。最大耐受剂量为2毫克/千克/天。剂量限制性毒性为感觉性周围神经病变,20例患者(55%)出现该症状。4例患者(11%)出现肝毒性。5例患者(14%)出现需要输血但无需停药的贫血。所有剂量水平下血浆消除半衰期的平均值±标准误为1.2±0.09小时。大多数患者的绝对CD4细胞计数增加或稳定。大多数可检测到血清p24抗原水平的患者在6个月时持续下降。d4T对艾滋病或ARC患者来说是一种有前景的药物。该临床试验正在继续以确定最小有效剂量。