Bhuyan B K, Adams E G, Johnson M, Crampton S L
Invest New Drugs. 1985;3(3):233-44. doi: 10.1007/BF00179427.
Menogarol is a new anthracycline undergoing phase I clinical trial. We report here the lethality after 2 hr exposure to 2 drug combinations of menogarol and several antitumor agents. A new statistical procedure was used to identify synergistic combinations. Most of these combinations were additive, except for menogarol plus melphalan, which was synergistic. Adriamycin plus melphalan was also synergistic. The menogarol-melphalan combination wa studied in detail with regard to the effect of dose and drug-schedule, lethality for exponential and plateau phase cells and effect on cell cycle progression. Although the combination was synergistic for exponential cells it was additive for plateau phase cells. The combination exerted a synergistic effect in inhibiting progression of cells through the cell cycle. After 2 hr menogarol exposure cells were blocked in G2 for about 12 hr following which the block was reversed. This reversal was inhibited when menogarol was combined with melphalan. The uptake of menogarol or melphalan was not changed in the presence of the other drug.
美诺加罗是一种正在进行I期临床试验的新型蒽环类药物。我们在此报告了美诺加罗与几种抗肿瘤药物的两种联合用药在暴露2小时后的致死率。采用了一种新的统计方法来确定协同组合。这些组合大多是相加作用,除了美诺加罗加美法仑具有协同作用外。阿霉素加美法仑也具有协同作用。对美诺加罗-美法仑组合在剂量和给药方案的影响、指数期和平稳期细胞的致死率以及对细胞周期进程的影响方面进行了详细研究。虽然该组合对指数期细胞具有协同作用,但对平稳期细胞却是相加作用。该组合在抑制细胞通过细胞周期进程方面发挥了协同作用。美诺加罗暴露2小时后,细胞在G2期被阻滞约12小时,随后阻滞被逆转。当美诺加罗与美法仑联合使用时,这种逆转受到抑制。在另一种药物存在的情况下,美诺加罗或美法仑的摄取没有改变。