R J Woodman, R L Cysyk, I Kline, M Gang, J M Venditti
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引用次数: 0
摘要
非白血病小鼠腹腔注射柔红霉素(1.8 mg/kg, q4d × 3),与ICRF-159同时腹腔注射可使LD50提高数倍。此外,用柔红霉素和ICRF-159治疗的白血病小鼠在L1210肿瘤细胞ip接种后第1、5和9天的存活率明显高于单独使用任何一种药物治疗后的存活率。这种联合治疗的生存增强通常发生在柔红霉素剂量大于单独柔红霉素LD50的情况下。单独皮下注射柔红霉素(14.0 mg/kg, q4d times 3)的LD50与ICRF-159联合治疗没有增加。然而,当白血病小鼠在注射L1210白血病细胞后的第1、5和9天分别用柔红霉素和ICRF-159治疗sc时,存活率高于单独使用任何一种药物治疗。ICRF-159并没有降低ip注射阿霉素的毒性,但与单独使用任何一种药物相比,联合使用这种药物治疗白血病小鼠在延长生存期方面更有效。柔红霉素加ICRF-159联合治疗对sc植入的L1210白血病的治疗效果明显低于对ip植入的肿瘤的治疗效果。
Enhancement of the effectiveness of daunorubicin (NSC-82151) or adriamycin (NSC-123127) against early mouse L1210 leukemia with ICRF-159 (NSC-129943).
The LD50 of intraperitoneally (ip) injected daunorubicin in nonleukemic mice (1.8 mg/kg, q4d times 3) can be increased several fold by the concomitant ip injection of ICRF-159. In addition, the survival of leukemic mice treated with daunorubicin and ICRF-159 on Days 1, 5, and 9 after ip inoculation of L1210 tumor cells was substantially greater than after treatment with either drug alone. This potentiation of survival with combination treatment usually occurred with doses of daunorubicin greater than the LD50 of daunorubicin alone. The LD50 of subcutaneously (sc) injected daunorubicin alone (14.0 mg/kg, q4d times 3) was not increased by concomitant ip treatment with ICRF-159. However, when leukemic mice were treated sc with daunorubicin and ip with ICRF-159 on Days 1, 5, and 9 after ip injection of L1210 leukemia cells, survival was greater than with treatment with either drug alone. The toxicity of ip injected adriamycin was not reduced by ICRF-159, but treatment of leukemic mice with this combination was more effective in prolonging survival than treatment with either drug alone. Combination treatment with daunorubicin plus ICRF-159 showed much less therapeutic enhancement against sc implanted L1210 leukemia than against the ip implanted tumor.