Overgaard J, Overgaard M, Nielsen O S, Pedersen A K, Timothy A R
Br J Cancer. 1982 Dec;46(6):904-11. doi: 10.1038/bjc.1982.300.
The hypoxic cell radiosensitizing properties of nimorazole have been investigated in a C3H mammary carcinoma transplanted to the feet of C3D2F1. The results have been compared with those obtained with misonidazole (MISO) in the same animal tumour system. For single-dose irradiation in air, nimorazole gives an enhancement ratio (ER) of approximately 1.4, independent of the dose of drug administered over the range 0.1-1.0 mg/g. MISO yields a similar ER at the 0.1 mg/g level but, unlike nimorazole, shows a steep dose-response curve with an ER of 2.2 when given in a concentration of 1.0 mg/g. No such dose-response relationship is seen with nimorazole despite the fact that tumour and plasma concentrations of the 2 drugs have an identical dose relationship. With irradiation given in 5 daily fractions, nimorazole and MISO at a dose of 0.3 mg/g per fraction both show an ER of approximately 1.3. The high drug doses used in single-fraction radiation experiments in animals bear little relation to those applicable to clinical practice since these would result in unacceptable toxicity. The results of the present studies are therefore of interest as nimorazole is potentially less toxic than MISO in humans but demonstrates similar radiosensitizing properties at clinically relevant dose levels.
已在移植到C3D2F1足部的C3H乳腺癌中研究了尼莫唑的乏氧细胞放射增敏特性。将结果与在相同动物肿瘤系统中使用米索硝唑(MISO)所获得的结果进行了比较。对于在空气中进行的单次照射,尼莫唑的增强比(ER)约为1.4,与给药剂量在0.1 - 1.0 mg/g范围内无关。MISO在0.1 mg/g水平时产生类似的ER,但与尼莫唑不同,当以1.0 mg/g的浓度给药时显示出陡峭的剂量反应曲线,ER为2.2。尽管两种药物的肿瘤和血浆浓度具有相同的剂量关系,但尼莫唑未观察到这种剂量反应关系。当以每日5次分割进行照射时,尼莫唑和MISO每分割剂量为0.3 mg/g时均显示出约1.3的ER。在动物单次分割放射实验中使用的高药物剂量与适用于临床实践的剂量几乎没有关系,因为这些剂量会导致不可接受的毒性。因此,本研究结果具有意义,因为尼莫唑在人体中的潜在毒性低于MISO,但在临床相关剂量水平下表现出类似的放射增敏特性。