Influence of azole antifungal drugs on blood tacrolimus levels after switching from intravenous tacrolimus to once‐daily modified release tacrolimus in patients receiving allogeneic hematopoietic stem cell transplantation

Summary What is known and objective Azole antifungal drugs are often co‐administered with tacrolimus after allogeneic hematopoietic stem cell transplantation (HSCT). However, the influence of azole antifungal drugs on variation in tacrolimus pharmacokinetics when switching from intravenous tacrolimu...

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Veröffentlicht in:Journal of clinical pharmacy and therapeutics 2019-08, Vol.44 (4), p.565-571, Article jcpt.12834
Hauptverfasser: Mimura, Akira, Yamaori, Satoshi, Ikemura, Noriaki, Katsuyama, Yoshihiko, Matsuzawa, Naoki, Ohmori, Shigeru
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Sprache:eng
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Zusammenfassung:Summary What is known and objective Azole antifungal drugs are often co‐administered with tacrolimus after allogeneic hematopoietic stem cell transplantation (HSCT). However, the influence of azole antifungal drugs on variation in tacrolimus pharmacokinetics when switching from intravenous tacrolimus (Tac‐iv) to once‐daily modified release tacrolimus (Tac‐MR) remains to be elucidated. This study was performed to evaluate the effects of oral azole antifungal drugs on variation in tacrolimus pharmacokinetics after conversion to Tac‐MR in HSCT patients. Methods Patients concomitantly receiving fluconazole (FLCZ) or voriconazole (VRCZ) along with tacrolimus were evaluated retrospectively. Blood tacrolimus concentrations before and after changing to oral administration were compared between FLCZ and VRCZ groups. Results and discussion A total of 52 patients (34 FLCZ and 18 VRCZ) were included in the analysis. There were no significant differences in the most recent daily dose (Div) and blood level (Civ) of Tac‐iv, Civ/Div, and ratio of daily dose of tacrolimus on the first to second day after changing to Tac‐MR (Dpo1‐2) to Div between FLCZ and VRCZ groups (P > 0.2). The trough levels of tacrolimus on the first to second day after switching to Tac‐MR (Cpo1‐2) and on the third to fifth day after the switch (Cpo3‐5) were significantly higher in the VRCZ group than the FLCZ group (P 
ISSN:0269-4727
1365-2710
DOI:10.1111/jcpt.12834