Guo Z G, Savaraj N, Feun L G, Lu K, Stewart D J, Luna M, Benjamin R S, Loo T L
Cancer Invest. 1983;1(6):475-8. doi: 10.3109/07357908309020272.
4'-(9-Acridinylamino)-methanesulfon-m-anisidide (AMSA) has shown significant antitumor activity against several murine tumors and leukemias. During its Phase I and II clinical trial, we were able to obtain tumors, plasma, and CSF specimens from patients who received varying doses of AMSA, as well as patients who received high doses and had autologous bone marrow rescue. The drug was analyzed chromatographically. The tumor to plasma drug concentration ratios ranged from 200% to 486%, apparently independent of dose and sampling time. Because AMSA was not detected in the CSF, the drug may not be effective in the treatment of meningeal metastasis. High-dose AMSA therapy with bone marrow rescue did not result in significantly higher AMSA concentrations in the tumor, nor did it elicit favorable response.
4'-(9-吖啶基氨基)-甲磺酰基间茴香胺(AMSA)已显示出对多种小鼠肿瘤和白血病具有显著的抗肿瘤活性。在其I期和II期临床试验期间,我们能够从接受不同剂量AMSA的患者以及接受高剂量并进行自体骨髓挽救的患者中获取肿瘤、血浆和脑脊液样本。对该药物进行了色谱分析。肿瘤与血浆药物浓度比在200%至486%之间,显然与剂量和采样时间无关。由于在脑脊液中未检测到AMSA,该药物可能对脑膜转移的治疗无效。高剂量AMSA联合骨髓挽救治疗并未导致肿瘤中AMSA浓度显著升高,也未引发良好反应。