Osswald H, Herrmann R, Youssef M
Cancer Lett. 1985 Dec;29(3):277-82. doi: 10.1016/0304-3835(85)90137-5.
The optimal synergism in combination therapy of leukemia L1210 depends on the sequence and the timing of the agents used. Etoposide (20 mg/kg applied intravenously) 3 h before methotrexate (50 mg/kg administered subcutaneously) results in significantly improved therapeutic action. Simultaneous application of these drugs, or an exceeding of that interval, do not entail synergism. Similar to the results obtained with other transplantable murine tumors, the optimal interval between methotrexate and 5-fluorouracil treatments of leukemia L1210 amounts to 6 h. Sequential treatment with etoposide (20 mg/kg given intravenously) significantly improves the efficacy of combined methotrexate (50 mg/kg applied subcutaneously) and 5-fluorouracil (80 mg/kg administered subcutaneously). The optimal synergism combining etoposide, methotrexate and 5-fluorouracil is achieved when the interval between etoposide and methotrexate amounts to 3 h followed 6 h later by 5-fluorouracil.
白血病L1210联合治疗中的最佳协同作用取决于所用药物的顺序和时间。在甲氨蝶呤(50mg/kg皮下注射)前3小时静脉注射依托泊苷(20mg/kg)可显著提高治疗效果。同时应用这些药物或超过该间隔时间均不会产生协同作用。与其他可移植小鼠肿瘤的结果相似,甲氨蝶呤和5-氟尿嘧啶治疗白血病L1210的最佳间隔时间为6小时。依托泊苷(20mg/kg静脉注射)序贯治疗可显著提高联合甲氨蝶呤(50mg/kg皮下注射)和5-氟尿嘧啶(80mg/kg皮下注射)的疗效。当依托泊苷与甲氨蝶呤之间的间隔为3小时,随后6小时给予5-氟尿嘧啶时,可实现依托泊苷、甲氨蝶呤和5-氟尿嘧啶联合的最佳协同作用。