Aapro M S, Alberts D S, Serokman R
Cancer Treat Rep. 1983 Nov;67(11):1013-7.
High-dose glucocorticosteroids have proven to be effective antiemetic agents when used before and after cisplatin chemotherapy. To rule out a possible decrease in cisplatin antitumor activity by a direct effect of short-term glucocorticosteroid treatment, survival was studied in mice inoculated with P388 leukemia and then treated with cisplatin preceded by a single high dose (1.5 mg/kg) of dexamethasone (Dex). The median survival of animals treated with cisplatin-Dex was 19 days, and that of animals treated with cisplatin alone was 18 days. These survival durations were significantly longer (P less than 0.01) than the survival time of the controls (median, 12 days). A double-layer soft agar clonogenic assay was used to study the possible effect of Dex on cisplatin inhibition of tumor colony-forming units from two human tumor cell lines (HEC-1A, endometrial; and WiDr, colon). In this model, the addition of Dex to cisplatin showed no statistically significant effect. These data suggest that Dex has no inhibitory effect on the antitumor activity of cisplatin.
高剂量糖皮质激素已被证明在顺铂化疗前后使用时是有效的止吐剂。为了排除短期糖皮质激素治疗的直接作用可能导致顺铂抗肿瘤活性降低的情况,对接种P388白血病的小鼠进行了生存研究,这些小鼠先接受单次高剂量(1.5mg/kg)地塞米松(Dex)治疗,然后再接受顺铂治疗。接受顺铂-Dex治疗的动物的中位生存期为19天,而仅接受顺铂治疗的动物的中位生存期为18天。这些生存期明显长于对照组的生存时间(中位值为12天)(P<0.01)。使用双层软琼脂克隆形成试验研究Dex对顺铂抑制两种人类肿瘤细胞系(HEC-1A,子宫内膜癌;WiDr,结肠癌)肿瘤集落形成单位的可能影响。在该模型中,将Dex添加到顺铂中未显示出统计学上的显著影响。这些数据表明Dex对顺铂的抗肿瘤活性没有抑制作用。