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首页> 外文期刊>Bone marrow transplantation >Modification of the pharmacokinetics of high-dose cyclophosphamide and cisplatin by antiemetics.
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Modification of the pharmacokinetics of high-dose cyclophosphamide and cisplatin by antiemetics.

机译:用止吐药修饰大剂量环磷酰胺和顺铂的药代动力学。

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Interpatient variability in exposure to certain chemotherapy agents can influence patient outcome, particularly with high-dose chemotherapy. We evaluated the possibility of a pharmacokinetic (PK) drug-drug interaction between the antiemetic agents and high-dose cyclophosphamide, cisplatin and BCNU (CPA/cDDP/BCNU). Twenty-three self-selected patients treated with high-dose CPA/cDDP/BCNU followed by autologous hematopoietic progenitor cell support (AHPCS) received ondansetron, lorazepam and diphenhydramine as antiemetics. PK parameters for each chemotherapeutic drug in the regimen were compared with those of 129 patients who received exactly the same chemotherapy but an antiemetic regimen substituting prochlorperazine for ondansetron. In addition, we performed a review of the English literature for reported drug-drug interactions between antiemetics and chemotherapy agents that led to modifications in any PK parameters of the chemotherapy agent. Our retrospective study showed that the mean area under the curve (AUC) for both cyclophosphamide (76,600 vs 90,600 microg/ml/min, P=0.001) and cisplatin (525 vs 648 microg/ml/min, P = 0.01) were significantly lower in the ondansetron group when compared with the prochlorperazine group. The AUC for BCNU was not significantly different in both groups (544 vs 677, P = 0.43). We found only one report of modifications of the PK parameters of high-dose chemotherapy agents due to drug-drug interactions with the most commonly used antiemetics in a review of the English literature between 1966 and 1995. We concluded that the AUC of high-dose cyclophosphamide and cisplatin are significantly lower when ondansetron, as opposed to prochlorperazine, is used as the antiemetic. The small sample size and heterogeneity of this group of patients precludes any outcome analysis of pharmacodynamic endpoints such as toxicity or antitumor effect. Nevertheless, the potential for interactions between antiemetics and chemotherapy agents should be taken into account when using different high-dose chemotherapy regimens.
机译:患者间接触某些化疗药物的差异会影响患者的预后,尤其是大剂量化疗时。我们评估了止吐药与大剂量环磷酰胺,顺铂和BCNU(CPA / cDDP / BCNU)之间发生药代动力学(PK)药物相互作用的可能性。 23例自选患者接受大剂量CPA / cDDP / BCNU治疗,然后接受自体造血祖细胞支持(AHPCS),并接受恩丹西酮,劳拉西m和苯海拉明作为止吐药。将方案中每种化疗药物的PK参数与接受完全相同的化学疗法但用止吐方案代替氯丙嗪代替恩丹西酮的129名患者的PK参数进行了比较。此外,我们对止吐药和化学治疗药物之间相互作用的药物相互作用的英文文献进行了综述,该相互作用导致化学治疗药物的任何PK参数发生变化。我们的回顾性研究表明,环磷酰胺(76,600 vs 90,600 microg / ml / min,P = 0.001)和顺铂(525 vs 648 microg / ml / min,P = 0.01)的曲线下面积(AUC)均显着降低恩丹西酮组与丙氯拉嗪组比较。两组的BCNU的AUC差异均无统计学意义(544对677,P = 0.43)。在1966年至1995年间对英国文献的综述中,我们仅发现了一份报告,该报告修改了大剂量化疗药物与最常用的止吐药之间的相互作用引起的大剂量化疗药物的PK参数。我们得出的结论是,大剂量的AUC当将昂丹西酮(与氯丙嗪相比)用作止吐药时,环磷酰胺和顺铂的含量要低得多。该组患者的样本量小且异质性使得无法进行药效学终点的任何结果分析,例如毒性或抗肿瘤作用。但是,当使用不同的大剂量化疗方案时,应考虑止吐药与化疗药物之间相互作用的可能性。

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