Marshall M E, Butler K, Cantrell J, Wiseman C, Mendelsohn L
Division of Hematology/Oncology, University of Kentucky Medical Center, Lexington 40536-0084.
Cancer Chemother Pharmacol. 1989;24(1):65-6. doi: 10.1007/BF00254109.
Based on previous results demonstrating that coumarin and cimetidine render objective tumor regressions in renal cell carcinoma, we conducted a pilot study to determine whether these drugs possess activity against malignant melanoma. A total of 22 patients with advanced melanoma received 100 mg coumarin p.o. daily for 14 days; on day 15, cimetidine was added at an oral dose of 300 mg four times daily. Both drugs were continued until progression of disease. In all, 12 patients had previously been treated, but all patients had a favorable performance status. No response was observed in 19 patients. Two patients with a low tumor burden achieved a partial response and a third showed a minor response. There was no toxicity from this regimen. Although coumarin and cimetidine at this dose and schedule did not display significant activity in this study population, further studies are warranted to explore higher doses and focus on patients with relatively low tumor burdens.
基于先前的结果表明香豆素和西咪替丁可使肾细胞癌出现客观的肿瘤消退,我们开展了一项初步研究,以确定这些药物对恶性黑色素瘤是否具有活性。共有22例晚期黑色素瘤患者接受每日口服100 mg香豆素,持续14天;在第15天,添加西咪替丁,口服剂量为每日4次,每次300 mg。两种药物均持续使用直至疾病进展。总共有12例患者先前接受过治疗,但所有患者的身体状况良好。19例患者未观察到反应。2例肿瘤负荷较低的患者获得部分缓解,第3例显示轻微反应。该治疗方案无毒性。尽管在此剂量和疗程下香豆素和西咪替丁在该研究人群中未显示出显著活性,但仍有必要进一步研究探索更高剂量,并关注肿瘤负荷相对较低的患者。