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Updated: Sep 21, 2026

An Ex vivo Assay to Study Candida albicans Hyphal Morphogenesis in the Gastrointestinal Tract
Published on: July 1, 2020
[Therapy of invasive organ mycoses in patients with systemic hematologic diseases]
1Medizinischen Klinik für Palliativmedizin des Evangelischen Johannes-Krankenhauses, Schildescher Strasse 99, D-33611 Bielefeld, Deutschland. Meinolf-Karthaus@johanneswerk.de
Abstract:
Fungal infections have increased substantially in patients with acute leukemia as well as in patients receiving allogeneic stem cell transplantations. Most frequently Aspergillus ssp. and Candida ssp. are observed. Despite the recent introduction of new azoles and lipid-based formulations of amphotericin B, there are few randomized, controlled studies on the use of antifungal drugs in patients with proven invasive fungal infections. Conventional Amphotericin B is considered gold standard for the treatment of invasive fungal infections, however is limited by nephrotoxicity and infusion related adverse events. Treatment with azoles, e.g. fluconazole, itraconazole or voriconazole is generally well-tolerated. Fluconazole, however, has no activity against Aspergillus ssp. An additional serious problem is an emerging resistance of non-albicans species to fluconazole. Lipid-formulations of amphotericin B seem to be attractive alternative, but considerably higher medical costs limit broader application of lipid formulations of amphotericin B. The current strategies for the treatment of documented fungal infections as well as the role of new antifungal agents are discussed in this review.
Insights
Fungal infections are rising in leukemia patients and transplant recipients. This review discusses current antifungal treatments, highlighting challenges with efficacy, toxicity, resistance, and cost.
Area of Science:
- Mycology
- Hematology
- Infectious Diseases
Background:
- Invasive fungal infections (IFIs) are increasingly prevalent in immunocompromised patients, particularly those with acute leukemia or undergoing allogeneic stem cell transplantation.
- Aspergillus and Candida species are the most common causative agents of IFIs in these vulnerable populations.
- Despite advancements, evidence from randomized controlled trials for antifungal therapies in proven IFIs remains limited.
Purpose of the Study:
- To review current treatment strategies for documented invasive fungal infections in immunocompromised patients.
- To evaluate the role and limitations of existing and novel antifungal agents.
- To discuss emerging challenges such as antifungal resistance and treatment costs.
Main Methods:
- Literature review focusing on antifungal drug efficacy, safety, and resistance patterns.
- Analysis of treatment guidelines and clinical trial data for invasive fungal infections.
- Discussion of conventional and newer antifungal agents, including azoles and amphotericin B formulations.
Main Results:
- Conventional Amphotericin B is the gold standard but associated with significant nephrotoxicity and infusion-related adverse events.
- Azoles (fluconazole, itraconazole, voriconazole) are generally well-tolerated but fluconazole lacks activity against Aspergillus and faces emerging resistance in non-albicans Candida species.
- Lipid formulations of amphotericin B offer an alternative but are limited by high costs.
Conclusions:
- Optimal management of IFIs in high-risk patients requires careful consideration of drug efficacy, toxicity, resistance profiles, and cost-effectiveness.
- Further research, including randomized controlled trials, is needed to establish optimal treatment strategies for IFIs.
- Emerging antifungal agents and formulations require thorough evaluation to address current therapeutic challenges.
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