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Model-Informed Dosing Optimization of Tacrolimus for Concomitant Administration with Itraconazole to Japanese Lung Transplant Recipients

伊曲康唑 他克莫司 药代动力学 医学 药理学 肺移植 相伴的 人口 治疗药物监测 移植 泌尿科 内科学 皮肤病科 抗真菌 环境卫生
作者
Ren Takahashi,Kotaro Itohara,Shunsaku Nakagawa,Y. Katada,Mitsuhiro Sugimoto,Keisuke Umemura,Katsuyuki Matsumura,Daiki Hira,Masahiro Tsuda,Yurie Katsube,Satona Tanaka,Akihiro Ohsumi,Daisuke Nakajima,Miki Nagao,Hiroshi Date,Tomohiro Terada
出处
期刊:Therapeutic Drug Monitoring [Lippincott Williams & Wilkins]
标识
DOI:10.1097/ftd.0000000000001249
摘要

Background: Tacrolimus is an immunosuppressant administered to patients undergoing lung transplantation. Itraconazole is often concomitantly used with tacrolimus to prevent fungal infections and increase tacrolimus concentration. However, the pharmacokinetics of tacrolimus in Japanese lung transplant recipients and the effect of itraconazole on its pharmacokinetics have not been adequately evaluated. Population pharmacokinetic analysis was conducted to develop an optimal dose adjustment method for use upon itraconazole initiation in Japanese lung transplant recipients. Methods: This study comprised Japanese lung transplant recipients whose blood tacrolimus and itraconazole concentrations were measured between January 2017 and December 2019. A nonlinear mixed-effects modeling program was used to explore the covariates of tacrolimus pharmacokinetics and effects of concomitant itraconazole use. Using the model, the optimal initial tacrolimus dose was calculated and a dose adjustment method comprising concomitant itraconazole use was developed. Results: A total of 1693 tacrolimus trough blood concentrations and 85 itraconazole trough plasma concentrations were obtained from 43 patients. Postoperative day, albumin level, and administration route were extracted as covariates for tacrolimus pharmacokinetics. The drug–drug interaction between tacrolimus and itraconazole could be predicted more accurately by considering the concentration-dependent inhibition of itraconazole. The optimal initial tacrolimus dose was 2.0 mg twice daily for tube and 1.5 mg twice daily for oral administration. To maintain the target concentration, the tacrolimus dose was reduced by 60% upon itraconazole initiation. Conclusions: This study is the first to use population pharmacokinetic analysis to assess the interaction between tacrolimus and itraconazole in patients who underwent lung transplantation. These results provide useful insights for optimizing the initial tacrolimus dose for concomitant itraconazole use.

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