Antitumor effects of pirarubicin and epirubicin in combination with doxifluridine and cisplatin against mouse P388 leukemia.

Cancer biochemistry biophysics Pub Date : 1995-11-01
N Agata, T Mase, H Izumi, S Hirano, H Iguchi, H Tone, T Takeuchi
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Abstract

In vivo antitumor activity of pirarubicin (THP) and epirubucin (EPI) in combination with doxifluridine (5'-DFUR) and cisplatin (CDDP) were examined using mouse P388 leukemia. THP (1.25-7.5 mg/kg) or EPI (1.25-15 mg/kg) was given intravenously on day 1, and then 5'-DFUR (125 or 250 mg/kg/day) and CDDP (4 mg/kg) were given orally on days 1-4 and intravenously on day 5 after tumor inoculation, respectively. Both THP and EPI enhanced the antitumor of a combination of 5'-DFUR and CDDP. The enhancement by THP was additive or synergistic, while that by EPI was additive. Cured animals were observed in the combination of THP with the two drugs, but not in that of EPI. Thus, in combination with 5'-DFUR and CDDP, THP was more effective against P388 leukemia than was EPI. The combination therapy using THP, 5'-DFUR and CDDP may be a novel chemotherapeutic approach to a variable type of tumors in clinical trials.

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吡柔比星、表柔比星联合多西氟定和顺铂抗小鼠P388白血病的作用。
以小鼠P388白血病为实验对象,观察吡柔比星(THP)、表柔比星(EPI)联合多西氟定(5’-DFUR)和顺铂(CDDP)的体内抗肿瘤活性。第1天静脉滴注THP (1.25 ~ 7.5 mg/kg)或EPI (1.25 ~ 15 mg/kg),肿瘤接种后第1 ~ 4天口服5′-DFUR(125、250 mg/kg),第5天静脉滴注CDDP (4 mg/kg)。THP和EPI均能增强5′-DFUR和CDDP的抗肿瘤作用。THP的增强是加性或协同性的,EPI的增强是加性的。两药联合使用THP均可治愈动物,而EPI未见治愈动物。因此,THP与5'-DFUR和CDDP联合治疗P388白血病比EPI更有效。在临床试验中,THP、5′-DFUR和CDDP联合治疗可能是一种新的化疗方法,用于治疗不同类型的肿瘤。
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