Abeloff M D, Rosen S T, Luk G D, Baylin S B, Zeltzman M, Sjoerdsma A
Cancer Treat Rep. 1986 Jul;70(7):843-5.
alpha-Difluoromethylornithine (DFMO), an irreversible inhibitor of ornithine decarboxylase, blocks polyamine synthesis and has demonstrated antitumor activity against small cell lung cancer and colon cancer in cell culture and animal tumor models. To evaluate clinical efficacy and further define toxic effects of this new agent, phase II trials of DFMO were performed in previously treated patients with advanced small cell lung cancer and previously untreated patients with metastatic colon cancer. Oral DFMO was administered at a dose of 2.25 g/m2/day every 6 hours continuously to patients with small cell lung cancer. The same dose was given to patients with colon cancer but on a schedule of "3 weeks on, 1 week off" to avoid hearing loss. Evaluation of toxicity indicated that thrombocytopenia was seen only in patients receiving continuous DFMO who had received prior chemotherapy, while reversible hearing loss and gastrointestinal side effects occurred on both intermittent and continuous schedules in previously treated and untreated patients.
α-二氟甲基鸟氨酸(DFMO)是鸟氨酸脱羧酶的不可逆抑制剂,可阻断多胺合成,并已在细胞培养和动物肿瘤模型中显示出对小细胞肺癌和结肠癌的抗肿瘤活性。为了评估这种新药的临床疗效并进一步明确其毒性作用,对先前接受过治疗的晚期小细胞肺癌患者和先前未接受过治疗的转移性结肠癌患者进行了DFMO的II期试验。对于小细胞肺癌患者,口服DFMO的剂量为2.25 g/m²/天,每6小时连续给药一次。给予结肠癌患者相同剂量,但采用“3周用药,1周停药”的方案以避免听力丧失。毒性评估表明,血小板减少仅见于接受过先前化疗且接受持续DFMO治疗的患者,而在先前接受过治疗和未接受过治疗的患者中,间歇性和持续性给药方案均出现了可逆性听力丧失和胃肠道副作用。