O'Donnell J F, Blakowski S A, Zacharski L R, Nierenberg D W, Coughlin C T, Fein S, Philipp E, Cornwell G G
Am J Clin Oncol. 1986 Apr;9(2):152-5. doi: 10.1097/00000421-198604000-00010.
Nafazatrom (Bay g 6575) has been shown to be a potent inhibitor of tumor metastasis in preclinical models. It is believed to work by stimulating endogenous prostacyclin production. The drug has also been shown to inhibit the growth of certain experimental tumors, to be cytostatic for certain cell lines in tissue culture, and to induce differentiation in HL-60, neuroblastoma, and Friend erythroleukemia cell lines. Furthermore, no toxicity has been seen in animals or human volunteers. We report here a clinical trial of oral nafazatrom at five dose levels in patients with advanced cancer. Thirty patients with a wide variety of advanced malignancies were treated for 26-638+ days (median 82 days). No tumor responses were seen. Toxicity included two cases with mild skin rashes, one case with nausea and vomiting, and one case with diarrhea. Nafazatrom is a safe and well-tolerated agent. Maximum activity would be predicted to occur in the adjuvant treatment of cancer and we feel that further efforts should proceed to identify the appropriate dose for such a trial.
萘法唑酮(Bay g 6575)在临床前模型中已被证明是一种有效的肿瘤转移抑制剂。据信它通过刺激内源性前列环素的产生而起作用。该药物还被证明可抑制某些实验性肿瘤的生长,对组织培养中的某些细胞系具有细胞抑制作用,并能诱导HL - 60、神经母细胞瘤和弗瑞德红白血病细胞系分化。此外,在动物或人类志愿者中未观察到毒性。我们在此报告一项针对晚期癌症患者口服萘法唑酮五个剂量水平的临床试验。30例患有多种晚期恶性肿瘤的患者接受了26至638 +天(中位数82天)的治疗。未观察到肿瘤反应。毒性包括2例轻度皮疹、1例恶心呕吐和1例腹泻。萘法唑酮是一种安全且耐受性良好的药物。预计其最大活性将出现在癌症的辅助治疗中,我们认为应进一步努力确定此类试验的合适剂量。