实现移植中免疫抑制药物定量的分析性能规范:观点文章。

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Maria Shipkova, Eberhard Wieland, Ekkerhard Schütz
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引用次数: 0

摘要

背景:分析方法需要满足临床需求的性能。有报道称,为药物分析设定允许分析不精密度目标(pCVA%)的方法各不相同。本研究的目的是采用 4 种不同的方法计算环孢素、他克莫司、依维莫司、西罗莫司和霉酚酸的 pCVA%,比较结果并认真讨论每种模型的优缺点:评估 pCVA% 的方法(A)基于作者实验室在 2022 年至 2023 年期间常规测量结果中观察到的生物变异,(B)根据药物的终末消除半衰期和给药间隔得出,(C 和 D)根据 2 种方法的治疗范围(TR)宽度进行探索。对于方法 A,分别评估了通过液相色谱-串联质谱法和电化学发光免疫分析法获得的环孢素和他克莫司的常规测量数据:结果:对于环孢素和他克莫司来说,四种不同的 pCVA% 计算方法得出的结果相似,但与分析方法有关。环孢素、他克莫司、依维莫司、西罗莫司和霉酚酸的平均 pCVA% 分别为 5.2%、5.6%、5.1%、4.8% 和 7.7%。采用 TR 相关方法实现的目标最具挑战性,而采用生物变异方法实现的目标则最容易达到。对于消除半衰期较长的药物(如依维莫司和西罗莫司),方法 B 的目标更为严格:结论:没有一种理想的药物分析目标设定方法。然而,各种方法得出的 pCVA% 值是相似的,并证实了以下几点
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toward Analytical Performance Specifications for Immunosuppressive Drug Quantification in Transplantation: An Opinion Article.

Background: Analytical methods require performance that meets the clinical needs. Different approaches for setting up permissible analytical imprecision goals (pCVA%) for drug analyses have been reported. The aim of this study was to calculate the pCVA% for cyclosporine, tacrolimus, everolimus, sirolimus, and mycophenolic acid using 4 alternative approaches, to compare the results and to critically discuss advantages and disadvantages of each model.

Methods: The approaches to evaluate pCVA% were (A) based on biological variation observed in routine measurement results between 2022 and 2023 in the authors' laboratory, (B) derived from the terminal elimination half-life and dosing interval of the drugs, and (C and D) explored from the width of the therapeutic ranges (TR) by the 2 methods. For approach A, routine measurement data for cyclosporine and tacrolimus, obtained through liquid chromatography-tandem mass spectrometry and electrochemiluminescence immunoassays, were evaluated separately.

Results: The 4 alternative approaches for deriving pCVA% yielded similar results, for cyclosporine and tacrolimus in an analytical method dependent manner. The average pCVA% was 5.2%, 5.6%, 5.1%, 4.8%, and 7.7% for cyclosporine, tacrolimus, everolimus, sirolimus, and mycophenolic acid, respectively. The most challenging goals were those using TR-related approaches, while those using the biological variation approach were most easily achievable. Approach B resulted in more stringent goals for drugs with longer elimination half-lives (eg, everolimus and sirolimus).

Conclusions: There is no single ideal approach for setting goals of drug analysis. However, the pCVA% values derived from the various approaches are similar and confirm that a <6% target proposed by the International Association of Therapeutic Drug Monitoring and Clinical Toxicology is adequate and realistic in combination with state-of-the-art measurement technologies. In the authors' opinion, approaches based on the width of the TR are preferable, as they represent a common basis for clinical decisions and reflect elements of biological variation and analytics used to establish the TR.

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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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