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肝肾功能移植后FK506全血浓度与疗效及毒性的关系。

Relationship of FK506 whole blood concentrations and efficacy and toxicity after liver and kidney transplantation.

作者信息

Kershner R P, Fitzsimmons W E

机构信息

Fujisawa USA, Inc., Deerfield, Illinois 60015, USA.

出版信息

Transplantation. 1996 Oct 15;62(7):920-6. doi: 10.1097/00007890-199610150-00009.

DOI:10.1097/00007890-199610150-00009
PMID:8878385
Abstract

FK506 (tacrolimus) is a safe and effective immunosuppressant for the prevention of organ rejection after organ transplantation. FK506 has a relatively narrow therapeutic index and the correlation of dose to blood concentration is poor as a result of moderate variability in pharmacokinetic parameters between patients. Therapeutic monitoring of whole blood FK506 drug concentrations has been used in an effort to determine whether a relationship exists between concentrations of FK506 in the blood and the development of toxicity or the risk for organ rejection. An analysis of the relationship between FK506 blood levels and the occurrence of toxicity and rejection was carried out using data from four recent clinical trials. Trough FK506 levels within a 7-day window before the onset of rejection or toxicity were analyzed using logistic regression models. In kidney transplant patients (n=92), a significant correlation between FK506 levels and the incidence of both toxicity (P=0.01) and rejection (P=0.02) was seen. In liver transplant patients from three clinical trials, FK506 levels correlated well with the incidence of toxicity (P < or = 0.01); however, there was no significant relationship between FK506 levels and the incidence of rejection. It is concluded that therapeutic monitoring of whole blood FK506 levels may be useful for minimizing the risks of both toxicity and rejection in kidney transplant patients and for minimizing the risk of toxicity in liver transplant recipients.

摘要

FK506(他克莫司)是一种安全有效的免疫抑制剂,用于预防器官移植后的器官排斥反应。FK506的治疗指数相对较窄,由于患者之间药代动力学参数存在适度变异性,剂量与血药浓度的相关性较差。对全血FK506药物浓度进行治疗监测,以确定血液中FK506浓度与毒性发生或器官排斥风险之间是否存在关联。利用最近四项临床试验的数据,对FK506血药浓度与毒性和排斥反应发生之间的关系进行了分析。使用逻辑回归模型分析排斥或毒性发作前7天内的FK506谷浓度。在肾移植患者(n=92)中,观察到FK506水平与毒性发生率(P=0.01)和排斥反应发生率(P=0.02)之间存在显著相关性。在三项临床试验的肝移植患者中,FK506水平与毒性发生率相关性良好(P≤0.01);然而,FK506水平与排斥反应发生率之间无显著关系。得出结论,对全血FK506水平进行治疗监测可能有助于将肾移植患者的毒性和排斥风险降至最低,并将肝移植受者的毒性风险降至最低。

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