Stewart F A, Luts A, Begg A C
Cancer Res. 1987 Feb 15;47(4):1016-21.
In this study the tolerance of previously irradiated kidneys to retreatment with chemotherapy was assessed. cis-Diamminedichloroplatinum(II) (c-DDP) was given to groups of mice at 1, 3, or 6 months after bilateral renal irradiation with single doses of 8-14 Gy. Renal function was measured monthly (by clearance of 51Cr ethylenediaminetetraacetic acid) from 4-35 weeks after c-DDP injection and results were compared with function after X-rays alone or drug alone. At early testing times (during the first 11 weeks after c-DDP injection) the renal function of mice given drug at 1 or 3 months after irradiation was very similar to that seen after drug alone. c-DDP given at 6 months caused slightly more damage than either drug or X-rays alone, but these results could be explained in terms of additive toxicities. At later testing times (11-35 weeks after c-DDP injection), renal function was much worse in all animals which had received previous irradiation, with the greatest damage when c-DDP was given 6 months after X-rays. This may be partly due to additional cell killing by the drug causing the expression of subclinical radiation injury. It is also possible that c-DDP pharmacokinetics was altered in animals with previously irradiated kidneys, leading to higher drug exposures in these mice.
在本研究中,评估了先前接受过照射的肾脏对再次化疗的耐受性。给双侧肾脏单次照射8 - 14 Gy后的小鼠分组在1、3或6个月时给予顺二氯二氨铂(c - DDP)。从注射c - DDP后4 - 35周每月测量肾功能(通过51Cr乙二胺四乙酸清除率),并将结果与单独接受X射线或单独接受药物后的肾功能进行比较。在早期检测时间(注射c - DDP后的前11周内),照射后1或3个月给予药物的小鼠肾功能与单独给予药物后的情况非常相似。6个月时给予c - DDP造成的损伤略大于单独给予药物或X射线,但这些结果可以用相加毒性来解释。在后期检测时间(注射c - DDP后11 - 35周),所有先前接受过照射的动物肾功能都差得多,在X射线照射后6个月给予c - DDP时损伤最大。这可能部分是由于药物导致亚临床放射性损伤的表达而造成额外的细胞杀伤。也有可能c - DDP的药代动力学在先前接受过肾脏照射的动物中发生了改变,导致这些小鼠体内药物暴露量更高。