Sasaki Y
Dept. of Medical Oncology, National Cancer Center.
Gan To Kagaku Ryoho. 1992 Apr;19(4):456-62.
Cis-Diamminedichloroplatinum (II) (cisplatin) is one of the key drugs in the treatment of solid tumors. Cis-Diammine-1, 1-cyclobutanedicarboxylateplatinum (II) (carboplatin) and cis-diammine (glycolato)-platinum (254-S) are second-generation platinum-coordination complexes developed in recent years not only to reduce nephrotoxicity but also to have antitumor activity equivalent or superior to cisplatin. Comparative pharmacological study among these three compounds was performed. Six different small cell lung cancer (SCLC) and six non-small cell lung cancer (NSCLC) lines were exposed to different concentration of the three platinum compounds, cisplatin, carboplatin and 254-S in colony assay. The IC50 values for cisplatin, carboplatin and 254-wS in SCLC cell lines were significantly lower than those in NSCLC cell lines. In addition, the IC50s for carboplatin were significantly higher than those for cisplatin and 254-S in both SCLC and NSCLC lines. A total of 15 patients entered the pharmacological study. In all, 80 mg/sqm cisplatin, 450 mg/sqm carboplatin, and 100 mg/sqm 254-S were each given to five patients by intravenous drip infusion over 30 min. Ultrafilterable platinum declined biexponentially for carboplatin and 254-S, whereas the free platinum of cisplatin fitted to a monoexponential equation. We reported the equation between nadir platelet count (NPC) and Ccr, by retrospective analysis in 38 "Training Set" patients; [NPC] = 2,783.4 x [Ccr.]- [NPC] = 2,783.4 x [Ccr.]- 64,264.7. To evaluate prospectively the equation in the "Test Set" patient and to refine it. Thirty four patients who entered phase II study of 254-S for NSCLC were prospectively analysed. Significant correlation was observed between observed NPC and predicted NPC which was calculated by the equation (R = 0.51). To refine the equation, all patients in both "Training Set" and "Test Set" were reanalyzed. Simple linear least model is shown as the best fit and refined equation is as follows: [NPC] = 2,201.7 x [Ccr.]-17,695.0. Bioassay was achieved by clonogenic techniques using NCI-H-69 (SCLC cell line) and PC-9 (NSCLC cell line) as target. Biological comparison was performed on the basis of the antitumor activity of patient's plasma using the antitumor index (ATI). The ATIs obtained by bioassay showed better correlation than the AUCs obtained by chemical assay with the clinical response for the three agents against SCLC and NSCLC according to the following equation: [Reported Response(%)] = 11.5668 + 0.0014 x [ATI] (r = 0.97).
顺二氯二氨铂(II)(顺铂)是治疗实体瘤的关键药物之一。顺二氨-1,1-环丁烷二羧酸铂(II)(卡铂)和顺二氨(乙醇酸根)铂(254-S)是近年来开发的第二代铂配位复合物,不仅用于降低肾毒性,而且具有与顺铂相当或更优的抗肿瘤活性。对这三种化合物进行了比较药理学研究。在集落试验中,将六种不同的小细胞肺癌(SCLC)和六种非小细胞肺癌(NSCLC)细胞系暴露于三种铂化合物顺铂、卡铂和254-S的不同浓度下。SCLC细胞系中顺铂、卡铂和254-S的IC50值显著低于NSCLC细胞系。此外,在SCLC和NSCLC细胞系中,卡铂的IC50均显著高于顺铂和254-S。共有15名患者进入药理学研究。分别给五名患者静脉滴注30分钟,剂量分别为顺铂80mg/m²、卡铂450mg/m²和254-S 100mg/m²。卡铂和254-S的可超滤铂呈双指数下降,而顺铂的游离铂符合单指数方程。通过对38名“训练集”患者的回顾性分析,我们报告了最低点血小板计数(NPC)与肌酐清除率(Ccr)之间的方程:[NPC]=2783.4×[Ccr]-64264.7。为了前瞻性地评估“测试集”患者中的方程并对其进行优化。对进入254-S治疗NSCLC II期研究的34名患者进行了前瞻性分析。观察到的NPC与通过该方程计算的预测NPC之间存在显著相关性(R=0.51)。为了优化方程,对“训练集”和“测试集”中的所有患者进行了重新分析。简单线性最小模型显示为最佳拟合,优化后的方程如下:[NPC]=2201.7×[Ccr]-17695.0。生物测定通过克隆技术实现,使用NCI-H-69(SCLC细胞系)和PC-9(NSCLC细胞系)作为靶标。使用抗肿瘤指数(ATI),基于患者血浆的抗肿瘤活性进行生物学比较。根据以下方程,通过生物测定获得的ATI与通过化学测定获得的AUC相比,与三种药物对SCLC和NSCLC的临床反应具有更好的相关性:[报告的反应(%)]=11.5668+0.0014×[ATI](r=0.97)。