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氯脲霉素的I期试验。

Phase I trial of chlorozotocin.

作者信息

Gralla R J, Tan C T, Young C W

出版信息

Cancer Treat Rep. 1979 Jan;63(1):17-20.

PMID:154363
Abstract

Chlorozotocin was given to 37 patients with advanced malignant tumors in a daily X 5 schedule at 6-week intervals. Total iv doses for each course ranged from 75 to 200 mg/m2. Myelosuppression was dose-limiting, with a platelet count depression regularly observed at doses of greater or equal to 150 mg/m2; leukopenia occurred only at the highest dose level. Nausea and vomiting were mild and uncommon. No hyperglycemia or adverse drug-related effects on renal or hepatic function were observed. No major antitumor activity occurred; however, three patients with renal cell carcinoma and one patient each with lung cancer, ovarian carcinoma, and Hodgkin's disease had minor objective decreases in tumor size. A dose range of 150--200 mg/m2 iv for each 5-day course is recommended for phase II studies.

摘要

对37例晚期恶性肿瘤患者给予氯脲霉素,采用每日1次,连续5天的给药方案,每6周为1个疗程。每个疗程的静脉注射总剂量为75至200mg/m²。骨髓抑制是剂量限制性毒性,当剂量大于或等于150mg/m²时,经常观察到血小板计数下降;白细胞减少仅在最高剂量水平出现。恶心和呕吐症状较轻且不常见。未观察到高血糖或药物对肾功能及肝功能的不良影响。未出现明显的抗肿瘤活性;然而,3例肾细胞癌患者以及各1例肺癌、卵巢癌和霍奇金病患者的肿瘤大小有轻微的客观缩小。推荐在II期研究中采用每个5天疗程静脉注射150 - 200mg/m²的剂量范围。

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引用本文的文献

1
Phase II study of chlorozotocin in islet cell carcinoma. A southwest Oncology Group study.氯脲霉素治疗胰岛细胞癌的II期研究。西南肿瘤协作组的一项研究。
Cancer Chemother Pharmacol. 1983;11(1):48-50. doi: 10.1007/BF00257417.
2
Phase I evaluation of chlorozotocin (NSC-178248): weekly schedule.氯脲霉素(NSC-178248)的I期评估:每周给药方案。
Invest New Drugs. 1985;3(1):57-62. doi: 10.1007/BF00176825.
3
Comparative interactions of streptozotocin and chlorozotocin with DNA of an insulin-secreting cell line (RINr).链脲佐菌素和氯脲佐菌素与胰岛素分泌细胞系(RINr)DNA的相互作用比较
Diabetologia. 1986 Mar;29(3):186-91. doi: 10.1007/BF02427091.