CNS-aspergillosis: are there new treatment options?

Mycoses. 2003:46 Suppl 2:8-14.

Abstract

Invasive aspergillosis is an increasing cause of morbidity and mortality in immunocompromised patients. Extension of invasive aspergillosis to the central nervous system (CNS) is associated with an exceeding high mortality which approaches 100%. One major factor contributing to this devastating outcome is a poor penetration into the CNS of frequently used antifungal drugs, such as amphotericin B or itraconazole. Voriconazole, a new triazole with broad activity against various fungi, including Aspergillus species, shows superior activity in invasive aspergillosis compared to treatment with conventional amphotericin B. Voriconazole readily penetrates the blood-brain barrier yielding fungicidal drug concentrations within the CNS. A growing number of patients with CNS aspergillosis has been successfully treated with voriconazole in recent years. The pharmacological properties, the broad antifungal activity and the promising clinical data suggest that the use of voriconazole in CNS aspergillosis might improve the outcome in this otherwise devastating clinical condition. However, additional clinical data are needed to determine more precisely the role of voriconazole in CNS aspergillosis. In this review, we have compiled the available pharmacological and clinical data on CNS aspergillosis.

Publication types

  • Review

MeSH terms

  • Amphotericin B / pharmacokinetics
  • Amphotericin B / pharmacology
  • Amphotericin B / therapeutic use
  • Antifungal Agents / pharmacokinetics
  • Antifungal Agents / pharmacology
  • Antifungal Agents / therapeutic use*
  • Aspergillosis / drug therapy*
  • Aspergillosis / microbiology
  • Blood-Brain Barrier
  • Caspofungin
  • Central Nervous System Fungal Infections / drug therapy*
  • Central Nervous System Fungal Infections / microbiology
  • Central Nervous System Fungal Infections / pathology
  • Echinocandins
  • Female
  • Flucytosine / pharmacokinetics
  • Flucytosine / pharmacology
  • Flucytosine / therapeutic use
  • Humans
  • Immunocompromised Host
  • Itraconazole / pharmacokinetics
  • Itraconazole / pharmacology
  • Itraconazole / therapeutic use
  • Lipopeptides
  • Male
  • Peptides / pharmacokinetics
  • Peptides / pharmacology
  • Peptides / therapeutic use
  • Peptides, Cyclic*
  • Pyrimidines / pharmacokinetics
  • Pyrimidines / pharmacology
  • Pyrimidines / therapeutic use
  • Triazoles / pharmacokinetics
  • Triazoles / pharmacology
  • Triazoles / therapeutic use
  • Voriconazole

Substances

  • Antifungal Agents
  • Echinocandins
  • Lipopeptides
  • Peptides
  • Peptides, Cyclic
  • Pyrimidines
  • Triazoles
  • Itraconazole
  • Amphotericin B
  • Flucytosine
  • Caspofungin
  • Voriconazole