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接受多胺生物合成抑制剂D,L-α-二氟甲基鸟氨酸治疗的癌症患者的尿多胺水平。

Urinary polyamine levels in cancer patients treated with D,L-alpha-difluoromethylornithine, an inhibitor of polyamine biosynthesis.

作者信息

Horn Y, Spigel L, Marton L J

机构信息

Department of Oncology, Assaf Harofeh Medical Center, Sackler School of Medicine, Zerifin, Israel.

出版信息

J Surg Oncol. 1989 Jul;41(3):177-82. doi: 10.1002/jso.2930410309.

Abstract

The polyamine biosynthesis inhibitor D,L-alpha-Difluoromethylornithine hydrochloride monohydrate (DFMO) has cytostatic and cytotoxic effects against various human tumor cell lines in vitro. We measured levels of the polyamines putrescine and spermidine in the urine of cancer patients undergoing "conventional" chemotherapy in a two-arm randomized phase I-II study with and without additional DFMO administered orally at a dose of 1.7 g/sq.m. t.i.d. The study group included 38 patients with carcinoma of the breast, stomach, prostate, or female genital organs or metastatic carcinoma of unknown origin. A control group of 32 patients with similar malignancies received "conventional" chemotherapy without DFMO. Polyamine levels were determined periodically in the urine of all patients. In DFMO-treated patients, a significant decrease in putrescine and spermidine levels was observed after 3 weeks of DFMO therapy (the first time point evaluated) that usually persisted throughout the course of treatment. Significant differences in polyamine levels between DFMO-treated and control patients were observed for patients in remission. Less significant differences were noted, however, for patients with static or progressive disease between DFMO-treated and control groups. DFMO activity appears to be reflected by a long-term decrease in urinary polyamine levels.

摘要

多胺生物合成抑制剂盐酸 D,L-α-二氟甲基鸟氨酸一水合物(DFMO)在体外对多种人类肿瘤细胞系具有细胞生长抑制和细胞毒性作用。在一项双臂随机 I-II 期研究中,我们测量了接受“传统”化疗的癌症患者尿液中的多胺腐胺和亚精胺水平,该研究分为两组,一组额外口服剂量为 1.7 g/平方米,每日三次的 DFMO,另一组不服用。研究组包括 38 例患有乳腺癌、胃癌、前列腺癌或女性生殖器官癌或不明来源转移性癌的患者。32 例患有类似恶性肿瘤的患者作为对照组,接受不含 DFMO 的“传统”化疗。定期测定所有患者尿液中的多胺水平。在接受 DFMO 治疗的患者中,DFMO 治疗 3 周后(第一个评估时间点)观察到腐胺和亚精胺水平显著下降,且在整个治疗过程中通常持续存在。对于缓解期患者,观察到 DFMO 治疗组和对照组之间的多胺水平存在显著差异。然而,对于病情稳定或进展的患者,DFMO 治疗组和对照组之间的差异不太显著。DFMO 的活性似乎通过尿多胺水平的长期下降得以体现。

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