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

Author:

Takahashi Ren1,Itohara Kotaro12ORCID,Nakagawa Shunsaku1,Katada Yoshiki1,Sugimoto Mitsuhiro1,Umemura Keisuke1,Matsumura Katsuyuki1,Hira Daiki1,Tsuda Masahiro1,Katsube Yurie1,Tanaka Satona3,Ohsumi Akihiro3,Nakajima Daisuke3,Nagao Miki4,Date Hiroshi3,Terada Tomohiro1

Affiliation:

1. Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital, Kyoto, Japan;

2. Department of Pharmacy, Kobe University Hospital, Kobe, Japan;

3. Department of Thoracic Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan; and

4. Department of Clinical Laboratory Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Abstract

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.

Funder

JSPS KAKENHI

Publisher

Ovid Technologies (Wolters Kluwer Health)

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