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一种用于估计肾移植后选定免疫抑制药物治疗指数的系统文献综述方法。

A Systematic Literature Review Approach to Estimate the Therapeutic Index of Selected Immunosuppressant Drugs After Renal Transplantation.

作者信息

Ericson Jessica E, Zimmerman Kanecia O, Gonzalez Daniel, Melloni Chiara, Guptill Jeffrey T, Hill Kevin D, Wu Huali, Cohen-Wolkowiez Michael

机构信息

*Department of Pediatrics, Pennsylvania State University, Hershey, PA;†Duke Clinical Research Institute, Durham, NC;‡Department of Pediatrics, Duke University, Durham, NC; and§Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC.

出版信息

Ther Drug Monit. 2017 Feb;39(1):13-20. doi: 10.1097/FTD.0000000000000364.

Abstract

BACKGROUND

Drugs that exhibit close margins between therapeutic and toxic blood concentrations are considered to have a narrow therapeutic index (NTI). The Food and Drug Administration has proposed that NTI drugs should have more stringent bioequivalence standards for approval of generic formulations. However, many immunosuppressant drugs do not have a well-defined therapeutic index (TI).

METHODS

We sought to determine whether safety, efficacy, and pharmacokinetic data obtained from the medical literature through a comprehensive literature search could be used to estimate the TI of cyclosporine, tacrolimus, and sirolimus. In this analysis, we considered TI ≤2 as a criterion to define a drug as having an NTI.

RESULTS

Published literature indicates that cyclosporine has a TI of 2-3, which falls just short of our criteria to be classified as having an NTI. We found sirolimus and tacrolimus to have a therapeutic range of 5-12 ng/mL and of 5-20 ng/mL, respectively, but were unable to calculate the TI.

CONCLUSIONS

Although the current literature does not provide a clear indication that these drugs have an NTI, the routine use of therapeutic drug monitoring in clinical practice suggests that more stringent testing of their pharmacokinetic and pharmacodynamic properties should be performed before the approval of generic formulations.

摘要

背景

治疗血药浓度与中毒血药浓度区间较窄的药物被认为具有窄治疗指数(NTI)。美国食品药品监督管理局提议,NTI药物在批准其仿制药时应具备更严格的生物等效性标准。然而,许多免疫抑制药物并没有明确界定的治疗指数(TI)。

方法

我们试图确定通过全面文献检索从医学文献中获取的安全性、有效性和药代动力学数据是否可用于估算环孢素、他克莫司和西罗莫司的TI。在此分析中,我们将TI≤2作为判定一种药物具有NTI的标准。

结果

已发表的文献表明环孢素的TI为2至3,略低于我们将其归类为具有NTI的标准。我们发现西罗莫司和他克莫司的治疗范围分别为5至12 ng/mL和5至20 ng/mL,但无法计算TI。

结论

虽然目前的文献并未明确表明这些药物具有NTI,但临床实践中治疗药物监测的常规使用表明,在批准仿制药之前,应对其药代动力学和药效学特性进行更严格的测试。

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