[Therapy of invasive organ mycoses in patients with systemic hematologic diseases]

M Karthaus1, A Böhme

  • 1Medizinischen Klinik für Palliativmedizin des Evangelischen Johannes-Krankenhauses, Schildescher Strasse 99, D-33611 Bielefeld, Deutschland. Meinolf-Karthaus@johanneswerk.de

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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