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腺苷脱氨酶抑制剂2'-脱氧助间型霉素的临床药理学。

The clinical pharmacology of the adenosine deaminase inhibitor 2'-deoxycoformycin.

作者信息

Smyth J F, Paine R M, Jackman A L, Harrap K R, Chassin M M, Adamson R H, Johns D G

出版信息

Cancer Chemother Pharmacol. 1980;5(2):93-101. doi: 10.1007/BF00435411.

Abstract

2'-deoxycoformycin (2'-dCF; Pentostatin), a stoichiometric inhibitor of mammalian adenosine deaminase (ado deaminase), exhibits immunosuppressive and antilymphocytic activity in animal test systems. A clinical pharmacology/phase I study of 2'-dCF administered as a single agent has been completed (18 patients). Dose levels ranged from 0.1 mg/kg X 1 to 0.25 mg/kg/day X 5; ado deaminase and 2'-dCF were measured spectrophotometrically. Plasma decay curves were bi-exponential (alpha and beta t 1/2 values about 1 and 10 h respectively). Recovery of unchanged 2'-dCF from urine (48 h) was 32%--48% of the administered drug. Major toxic manifestations were lymphocytopenia (all patients) and urate nephropathy (1 patient, with subsequent patients in the series receiving allopurinol, 300 mg/day). Three partial responses were seen in seven patients with acute lymphocytic leukaemia receiving 0.25 mg 2'-dCF/kg/day X 5.

摘要

2'-脱氧助间型霉素(2'-dCF;喷司他丁)是一种哺乳动物腺苷脱氨酶(ado脱氨酶)的化学计量抑制剂,在动物试验系统中表现出免疫抑制和抗淋巴细胞活性。一项关于单药使用2'-dCF的临床药理学/Ⅰ期研究已经完成(18例患者)。剂量范围为0.1mg/kg×1至0.25mg/kg/天×5;采用分光光度法测定ado脱氨酶和2'-dCF。血浆衰减曲线为双指数型(α和β半衰期值分别约为1小时和10小时)。尿中未变化的2'-dCF回收率(48小时)为给药剂量的32%至48%。主要毒性表现为淋巴细胞减少(所有患者)和尿酸盐肾病(1例患者,后续患者系列中接受300mg/天别嘌呤醇)。7例接受0.25mg 2'-dCF/kg/天×5的急性淋巴细胞白血病患者中有3例部分缓解。

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