de Jonge Maja J A, Glimelius B, Verweij Jaap, Van Groeningen C, Bonneterre J, de Vries E G E, Culine S, Young J, Smith Rob, Droz J
Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital, The Netherlands.
Anticancer Drugs. 2002 Jul;13(6):645-53. doi: 10.1097/00001813-200207000-00012.
ZD9331 is a potent thymidylate synthase inhibitor. Renal and hepatic clearances were found to be important routes of elimination. The objectives of this pharmacologic trial were to investigate the effect of renal impairment on the pharmacokinetics of ZD9331, to study the toxicity profile and to document any antitumor effects of ZD9331 when administered i.v. to patients with different degrees of renal impairment. Patients were treated with ZD9331 130 mg/m2 given as an i.v. infusion on day 1 of a 4-week cycle to allow full pharmacokinetic assessment. Subsequent cycles involved the administration of ZD9331 on days 1 and 8, every 3 weeks. Patients were stratified according to their renal function assessed by the creatinine clearance: normal renal function (creatinine clearance > or =60 ml/min), mildly impaired renal function (creatinine clearance > or =40 to <60 ml/min) and moderately impaired renal function (creatinine clearance >25 to <40 ml/min). For pharmacokinetic analysis plasma sampling was performed during the first course and assayed using a validated liquid chromatographic tandem mass spectrometry assay. Twenty-three patients were entered on the study, of whom 21 received 130 mg/m2 ZD9331 in the first treatment cycle. No relationship was seen between renal impairment and plasma clearance nor with the area under the concentration-time curve of free ZD9331. Increasing renal impairment was associated with a greater incidence of myelosuppression. No predictive relationship between the clearance of free ZD9331 and the degree of renal impairment as determined by creatinine clearance could be assessed. However, data from this trial indicate that increased renal impairment may be associated with greater ZD9331-induced toxicity, particularly myelosuppression, although this cannot be attributed to any alteration in the plasma pharmacokinetics of ZD9331. Therefore, it may be necessary to administer a reduced dose of ZD9331 to patients with impaired renal function.
ZD9331是一种强效胸苷酸合成酶抑制剂。已发现肾脏和肝脏清除是重要的消除途径。本药理学试验的目的是研究肾功能损害对ZD9331药代动力学的影响,研究毒性特征,并记录静脉注射ZD9331对不同程度肾功能损害患者的任何抗肿瘤作用。患者在4周周期的第1天接受130mg/m²的ZD9331静脉输注治疗,以进行全面的药代动力学评估。后续周期为每3周在第1天和第8天给予ZD9331。根据通过肌酐清除率评估的肾功能对患者进行分层:肾功能正常(肌酐清除率≥60ml/分钟)、轻度肾功能损害(肌酐清除率≥40至<60ml/分钟)和中度肾功能损害(肌酐清除率>25至<40ml/分钟)。为进行药代动力学分析,在第一个疗程期间采集血浆样本,并使用经过验证的液相色谱串联质谱分析法进行测定。23名患者进入该研究,其中21名在第一个治疗周期接受了130mg/m²的ZD9331。未发现肾功能损害与血浆清除率之间以及与游离ZD9331浓度-时间曲线下面积之间存在相关性。肾功能损害加重与骨髓抑制发生率增加相关。无法评估游离ZD9331的清除率与通过肌酐清除率确定的肾功能损害程度之间的预测关系。然而,该试验的数据表明,肾功能损害加重可能与ZD9331诱导的毒性增加有关,尤其是骨髓抑制,尽管这不能归因于ZD9331血浆药代动力学的任何改变。因此,可能有必要对肾功能受损的患者给予降低剂量的ZD9331。