2026/02/13 by Felix Bergmann, Marlene Prager, Lena Pracher +3 · 1 voice
Medicine · #Antifungal resistance and susceptibility #Antibiotics Pharmacokinetics and Efficacy #Fungal Infections and Studies
paper · doi:10.1016/j.ijantimicag.2026.107743
openalex created_date 2026/02/13 · openalex publication_date 2026/02/13 · openalex updated_date 2026/07/09
Invasive fungal infections are a major cause of morbidity and mortality in immunocompromised and critically ill patients. While plasma pharmacokinetics (PK) commonly guide antifungal dosing, they may not reliably reflect drug exposure at infection sites, particularly in compartments that are difficult to reach. Tissue PK is increasingly recognised as an important determinant of optimal dosing and therapeutic success. This review summarises available clinical data on tissue PK of approved antifungal agents, including triazoles, echinocandins, amphotericin B formulations, and flucytosine. Studies were identified via a PubMed search through July 2025, focusing on prospective human trials reporting both plasma and tissue concentrations. Our findings revealed marked variability in tissue penetration across drugs and compartments. These findings underscore the limitations of relying solely on plasma concentrations to estimate tissue exposure and emphasise the importance of considering tissue penetration when selecting and dosing antifungal therapy.