Klein H O, Wickramanayake P D, Christian E, Coerper C
Cancer. 1984 Sep 15;54(6 Suppl):1193-203. doi: 10.1002/1097-0142(19840915)54:1+<1193::aid-cncr2820541317>3.0.co;2-z.
This report describes some experimental and clinical studies showing the following: (1) in animals under protection of mesna the dose of ifosfamide (Ifo) can be increased significantly; (2) fractionated administration of Ifo, cyclophosphamide (CPA), or the stabilized metabolite of cyclophosphamide (ASTA Z 7557) is less toxic than single push-injection of the same total daily dose and therapeutically more effective; and (3) in humans under the protection of mesna the continuous infusions of ifosfamide over 5 days leads to an increase of the MTD compared with single daily short-term infusion and responses in some solid tumors, e.g., soft tissue sarcomas.
本报告描述了一些实验和临床研究,结果如下:(1)在美司钠保护下的动物中,异环磷酰胺(Ifo)的剂量可显著增加;(2)异环磷酰胺、环磷酰胺(CPA)或环磷酰胺的稳定代谢物(ASTA Z 7557)分次给药的毒性低于相同每日总剂量的单次推注,且治疗效果更佳;(3)在美司钠保护下的人类中,与每日单次短期输注相比,异环磷酰胺连续5天输注可提高最大耐受剂量(MTD),并对一些实体瘤,如软组织肉瘤产生反应。