Related Experiment Video
Updated: Oct 23, 2025

An Ex vivo Assay to Study Candida albicans Hyphal Morphogenesis in the Gastrointestinal Tract
Published on: July 1, 2020
Clinical Considerations of Isavuconazole Administration in High-Risk Hematological Patients: A Single-Center 5-Year
Ilona Kronig1, Stavroula Masouridi-Levrat2, Yves Chalandon2
1Division of Infectious Diseases, University Hospital of Geneva, Rue Gabrielle-Perret-Gentil 4, 1211, Geneva, Switzerland.
Background:
There are limited real-life data on isavuconazole prophylaxis and treatment of invasive mold infections (IMI) in hematological patients and allogeneic hematopoietic cell transplant (HCT) recipients.
Objectives:
Primary objective was to describe the indications of real-life isavuconazole administration at a university hospital. Secondary objectives included the description of liver function tests and QTc interval between baseline and end of treatment (EOT), clinical outcomes and breakthrough IMI by the EOT.
Patients/Methods:
This was a 5-year single-center retrospective study of all adult patients with acute myeloid leukemia and/or allogeneic HCT recipients who received isavuconazole as prophylaxis and/or treatment between June 1, 2016, and July 31, 2020.
Results:
Among 30 identified patients, the indications for isavuconazole administration were adverse events associated with prior antifungal treatment (N: 18, 60%: hepatotoxicity, renal insufficiency, long QTc interval, neurotoxicity, and potential drug-drug interactions in 6, 4, 3, 1 and 4 patients, respectively), clinical efficacy (N: 5, 16.6%), and other reasons (N: 10, 33.3%; 5/10 patients treated with isavuconazole to facilitate hospital discharge with orally administered appropriate treatment). Alanine aminotransferase significantly decreased from baseline (mean: 129 IU/L, range: 73, 202) to a mean of 48 IU/L (range: 20, 80) by day 14 (P-value: 0.02), 23.5 IU/L (range: 20, 27) by day 28 (P-value: 0.03) and 16.5 IU/L (range: 16, 17) by day 42 (P-value: 0.009). The QTc interval decreased from baseline (mean: 456.8 ms, range: 390, 533) to EOT (mean: 433.8 ms, range: 400, 472; P-value: 0.03). The mean isavuconazole plasma concentration was 2.9 mg/L (range: 0.9, 6.7). There was no breakthrough IMI observed.
Conclusion:
Isavuconazole is a safe and reliable antifungal agent in complex hematological patients, with relatively low hepatotoxicity and QTc interval shortening properties.
Insights
Isavuconazole is a safe antifungal for hematological patients, showing reduced liver enzymes and QTc interval shortening. This real-world study confirms its efficacy in preventing and treating invasive mold infections (IMI).
Area of Science:
- Mycology
- Hematology
- Pharmacology
Background:
- Limited real-world data exists on isavuconazole for invasive mold infections (IMI) in hematological patients and allogeneic hematopoietic cell transplant (HCT) recipients.
- Isavuconazole is a broad-spectrum triazole antifungal agent.
Purpose of the Study:
- To describe real-world indications for isavuconazole use in a university hospital.
- To evaluate liver function tests, QTc interval, clinical outcomes, and breakthrough IMI during isavuconazole therapy.
Main Methods:
- A 5-year retrospective study (June 2016 - July 2020) of adult hematological patients and HCT recipients receiving isavuconazole.
- Data collected included indications for use, laboratory values, QTc interval, and clinical outcomes.
Main Results:
- Isavuconazole was administered for adverse events of prior antifungals (60%), clinical efficacy (16.6%), and other reasons (33.3%).
- Significant decreases in alanine aminotransferase and QTc interval were observed.
- No breakthrough invasive mold infections (IMI) occurred.
Conclusions:
- Isavuconazole demonstrates safety and reliability in complex hematological patients.
- The agent exhibits favorable properties, including low hepatotoxicity and QTc interval shortening.
More Related Videos
10:42Ex Vivo Expansion of Hematopoietic Stem Cells from Human Umbilical Cord Blood-derived CD34+ Cells Using Valproic Acid
Published on: April 11, 2019
08:52Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
Related Concept Videos
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions
Drug Dosage Regimen: Overview
Typically, the starting dose and dosing interval are guided by the manufacturer's recommendations based on clinical trials conducted during and after drug...
Drug Dosing: Geriatric Patients
Bioavailability Study Design: Healthy Subjects Versus Patients
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow