Literature DB >> 35088349

Differences in kinetics of tacrolimus concentration after letermovir discontinuation by type of concomitant azole antifungal.

Toshihisa Nakashima1, Yoshihiro Inamoto2, Jun Aoki3, Ayumu Ito3, Takashi Tanaka3, Sung-Won Kim3, Hironobu Hashimoto1, Takahiro Fukuda3, Tetsuya Furukawa1.   

Abstract

Letermovir is commonly used for CMV prophylaxis after allogeneic hematopoietic cell transplantation (HCT). Pharmacokinetic studies have shown an increase in tacrolimus exposure among healthy volunteers who took letermovir. However, studies in HCT recipients are needed because these patients are typically using concomitant antifungals with different degrees of CYP3A4 inhibition that may further interact with tacrolimus pharmacokinetics. In this study, we retrospectively evaluated the kinetics of tacrolimus concentration after letermovir discontinuation by type of concomitant azole antifungal in 57 HCT recipients. The median fold change in tacrolimus concentration-to-dose (C/D) ratio after discontinuing letermovir was 0.64 (range 0.43-0.99) with fluconazole and 1.10 (range 0.59-1.73) with voriconazole (p < 0.001). The tacrolimus C/D ratio decreased ≥ 30% after discontinuing letermovir (p < 0.001) in 66% of patients on fluconazole and 9% on voriconazole. Among patients whose tacrolimus C/D ratio decreased ≥ 30%, three (9%) patients in the fluconazole group and one (4%) in the voriconazole group experienced worsening of GVHD. Careful monitoring of tacrolimus concentration is important after letermovir discontinuation to avoid worsening of GVHD due to decreased tacrolimus concentration.
© 2021. Japanese Society of Hematology.

Entities:  

Keywords:  Allogeneic hematopoietic stem cell transplantation; Azole antifungal agent; Drug–drug interaction; Letermovir; Tacrolimus

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Year:  2022        PMID: 35088349     DOI: 10.1007/s12185-021-03277-6

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  1 in total

Review 1.  Drug-drug interactions between triazole antifungal agents used to treat invasive aspergillosis and immunosuppressants metabolized by cytochrome P450 3A4.

Authors:  Andreas H Groll; Robert Townsend; Amit Desai; Nkechi Azie; Mark Jones; Marc Engelhardt; Anne-Hortense Schmitt-Hoffman; Roger J M Brüggemann
Journal:  Transpl Infect Dis       Date:  2017-09-28       Impact factor: 2.228

  1 in total
  1 in total

1.  Interactions with the CYP3A inhibitor voriconazole differ between extended-LCP- and immediate-release tacrolimus formulations.

Authors:  Gerold Thölking; Ulrich Jehn; Stefan Reuter
Journal:  Int J Hematol       Date:  2022-04-09       Impact factor: 2.490

  1 in total

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