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患者因素对秋水仙碱群体药代动力学的影响:对安全有效给药的启示

The Influence of Patient Factors on the Population Pharmacokinetics of Colchicine: Implications for Safe and Effective Dosing.

作者信息

Wright Daniel F B, Hishe Hailemichael Z, Dalbeth Nicola, Horne Anne, Drake Jill, Haslett Janine, Stamp Lisa K

机构信息

Faculty of Medicine and Health, Sydney Pharmacy School, University of Sydney, Sydney, 2006, Australia.

Department of Clinical Pharmacology & Toxicology, St. Vincent's Hospital Sydney, Darlinghurst, Australia.

出版信息

Clin Pharmacokinet. 2025 Oct;64(10):1517-1529. doi: 10.1007/s40262-025-01551-y. Epub 2025 Jul 28.

Abstract

BACKGROUND AND OBJECTIVES

The factors that predict colchicine plasma concentrations and the impact on safety and efficacy are under-researched. We aimed to determine the probability of achieving steady-state plasma concentrations within the nominal therapeutic range of 0.5-3 ng/mL.

METHODS

Colchicine plasma concentrations from 78 people with gout were analysed using non-linear mixed effects. Body size, kidney function, concomitant drugs, ethnicity, sex, age and adherence were tested as covariates in the model. Simulations were conducted to determine the probability of achieving steady-state minimum, maximum and average concentrations within the therapeutic range of 0.5-3 ng/mL under different doses and for different patient characteristics. We considered colchicine doses that produced > 80% of steady-state average concentrations < 3 ng/mL and > 0.5 ng/mL to have a reasonable probability of safety and efficacy.

RESULTS

A two-compartment pharmacokinetic model with zero-order absorption was the best fit. Body weight, sex and statin use were significant predictors of colchicine pharmacokinetics, reducing the between-subject variance on clearance by about 40%. The model predicted that colchicine dosages of ≤ 1.5 mg daily carry a low risk of toxicity based on the criteria defined here. Efficacious concentrations were achieved for all dosages tested except 0.5 mg daily, where concentrations below the proposed therapeutic range may occur in those with a body weight > 80 kg. Higher colchicine dosages of > 1.5 mg daily may exceed the proposed upper limit of safety in many individuals, particularly those with low body weight who are taking statins.

CONCLUSION

A model for the pharmacokinetics of colchicine was developed and evaluated. Low-dose regimes (≤ 1.5 mg daily) are not predicted to achieve concentrations above the proposed safety threshold of 3 ng/mL in most people, although concentrations below the lower limit of the therapeutic range may occur in those taking 0.5-mg doses who are > 80 kg in body weight. Higher colchicine dosages of > 1.5 mg daily may exceed the proposed upper limit of safety in individuals with low body weight who are taking statins.

摘要

背景与目的

预测秋水仙碱血浆浓度的因素以及对安全性和疗效的影响研究不足。我们旨在确定在0.5 - 3 ng/mL的标称治疗范围内达到稳态血浆浓度的概率。

方法

使用非线性混合效应分析78例痛风患者的秋水仙碱血浆浓度。在模型中测试了体型、肾功能、伴随用药、种族、性别、年龄和依从性作为协变量。进行模拟以确定在不同剂量和不同患者特征下,在0.5 - 3 ng/mL治疗范围内达到稳态最低、最高和平均浓度的概率。我们认为产生>80%稳态平均浓度<3 ng/mL且>0.5 ng/mL的秋水仙碱剂量具有合理的安全性和疗效概率。

结果

具有零级吸收的二室药代动力学模型拟合最佳。体重、性别和他汀类药物的使用是秋水仙碱药代动力学的显著预测因素,使清除率的个体间差异降低约40%。根据此处定义的标准,该模型预测每日秋水仙碱剂量≤1.5 mg时毒性风险较低。除了每日0.5 mg的剂量外,所有测试剂量均达到了有效浓度,对于体重>80 kg的患者,每日0.5 mg剂量可能会出现低于建议治疗范围的浓度。每日秋水仙碱剂量>1.5 mg可能会超过许多个体建议的安全上限,特别是那些体重低且正在服用他汀类药物的个体。

结论

开发并评估了秋水仙碱的药代动力学模型。低剂量方案(每日≤1.5 mg)预计在大多数人中不会达到高于建议安全阈值3 ng/mL的浓度,尽管体重>80 kg且服用0.5 mg剂量的患者可能会出现低于治疗范围下限的浓度。每日秋水仙碱剂量>1.5 mg可能会超过体重低且正在服用他汀类药物的个体建议的安全上限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ad/12479679/62578f46b768/40262_2025_1551_Fig1_HTML.jpg

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