Pilot phase I-II study on 5-aza-2'-deoxycytidine (Decitabine) in patients with metastatic lung cancer

被引:184
作者
Momparler, RL
Bouffard, DY
Momparler, LF
Dionne, J
Belanger, K
Ayoub, J
机构
[1] UNIV MONTREAL, DEPT PHARMACOL, MONTREAL, PQ H3C 3J7, CANADA
[2] HOP NOTRE DAME DE BON SECOURS, CTR ONCOL, MONTREAL, PQ H2L 1R7, CANADA
关键词
5-Aza-2'-deoxycytidine; clonogenic assay; hematopoietic toxicity; lung cancer; pharmacokinetics;
D O I
10.1097/00001813-199704000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
5-Aza-2'-deoxycytidine (5-AZA-CdR, Decitabine) is a nucleoside analog and an active drug for the therapy of acute leukemia. The incorporation of 5-AZA-CdR into DNA blocks DNA methylation and can result in the activation of specific genes, such as tumor suppressor genes, This novel mechanism of action of 5-AZA-CdR stimulated our interest in its potential for cancer therapy in patients with rung cancer, Using a colony assay we observed that 5-AZA-CdR showed a potent antineoplastic effect against two human lung carcinoma cell lines. The objective of this preliminary phase I-II study was to evaluate the toxicity and clinical efficacy of 5-AZA-CdR in patients with stage IV non-small cell lung carcinoma, there were 15 patients that entered the clinical study. Far nine assessable patients that received 5-AZA-CdR by a single 8 h i.v. infusion of 200-660 mg/m(2) for one or more cycles, the median survival duration was 6.7 months, with three patients surviving more than 15 months. The steady-state plasma concentration of 5-AZA-CdR during the infusion was estimated in some patients and was In the same range that produced activation of a tumor suppressor gene in human lung tumor cell lines as reported by other investigators. The major side effect of 5-AZA-CdR was hematopoietic toxicity which required a 5-6 week recovery period before the next cycle of therapy. This study suggests that 5-AZA-CdR may have some clinical activity against metastatic lung carcinoma using this type of dose schedule.
引用
收藏
页码:358 / 368
页数:11
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