Isavuconazole as prophylaxis and therapy for invasive fungal diseases: a real-life observational study

Author:

Ergün Mehmet12,Jansen Anouk M E13ORCID,Hilbrands Luuk B4ORCID,de Kort Elizabeth15ORCID,Kunst Henricus67,Reijers Monique H E18,Schouten Jeroen A910,Verweij Paul E12ORCID,Brüggemann Roger J M13ORCID

Affiliation:

1. Radboudumc—CWZ Center of Expertise for Mycology, Radboud University Medical Center , Nijmegen , The Netherlands

2. Department of Medical Microbiology, Radboud University Medical Center , Nijmegen , The Netherlands

3. Department of Pharmacy, Radboud University Medical Center , Nijmegen , The Netherlands

4. Department of Nephrology, Radboud University Medical Center , Nijmegen , The Netherlands

5. Department of Haematology, Radboud University Medical Center , Nijmegen , The Netherlands

6. Department of Otorhinolaryngology, Dutch Academic Alliance Skull Base Pathology, Radboud University Medical Centre , Nijmegen , The Netherlands

7. Department of Otorhinolaryngology, Dutch Academic Alliance Skull Base Pathology, Maastricht University Medical Center+ , Maastricht , The Netherlands

8. Department of Pulmonology, Radboud University Medical Center , Nijmegen , The Netherlands

9. Department of Intensive Care Medicine, Radboud University Medical Center , Nijmegen , The Netherlands

10. Scientific Centre for Quality of Healthcare (IQ healthcare), Radboud Institute for Health Sciences , Nijmegen , The Netherlands

Abstract

Abstract Background Isavuconazole is a relatively new antifungal agent indicated for the management of various invasive fungal diseases (IFDs), including invasive aspergillosis. Information on real-world experience with isavuconazole is scarce. This retrospective observational study aimed to describe the usage of isavuconazole in clinical practice with an in-depth evaluation of individual isavuconazole exposure. Methods Patients treated with isavuconazole were evaluated based on retrospective data, including therapeutic drug monitoring (TDM) data and efficacy and safety data. Additionally, we calculated the individual isavuconazole exposure described by the average AUC24 over the first 7 days of treatment by means of non-linear mixed-effects modelling and compared this with the currently desired lower target AUC of 60 mg·h/L. Results Ninety-nine patients treated with isavuconazole were evaluated. In our real-life cohort, isavuconazole was often deployed off-label in patients with non-classical host factors and infections with non-Aspergillus and non-Mucorales species. Isavuconazole was most often chosen for its safety profile, even after prior triazole treatment with manifestations of toxicity. TDM and subsequent dosage adjustments were frequently performed. The individual average AUC24 over 7 days was above 60 mg·h/L in 29 out of 77 (37.7%) patients. Conclusions This overview provides practical insights that can aid clinicians in the management of their patients with IFD. Our study shows that isavuconazole was used in a diverse patient population and was well tolerated overall. Individual isavuconazole exposure reflected by the average AUC24 over the first 7 days of treatment was generally low and variable. Dosage adjustments following TDM were frequently performed. Our experience shows that isavuconazole is a feasible alternative after prior azole treatment.

Funder

Pfizer

Publisher

Oxford University Press (OUP)

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