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Itraconazole in the treatment of aspergillosis: a study of 16 cases

B Lebeau1, H Pelloux, C Pinel

  • 1Service de Parasitologie-Mycologie, CHU, Grenoble, France.

Mycoses
|June 1, 1994
PubMed

Insights

Itraconazole shows promise for treating various forms of aspergillosis, with nine out of sixteen patients responding positively. However, relapses and liver issues necessitate careful monitoring during antifungal therapy.

Area of Science:

  • Mycology
  • Pharmacology
  • Infectious Diseases

Background:

  • Aspergillosis is a serious fungal infection caused by Aspergillus species.
  • Itraconazole is a novel triazole antifungal with demonstrated in vitro activity against filamentous fungi, including Aspergillus.
  • Limited clinical data exists on itraconazole's efficacy across different aspergillosis manifestations.

Observation:

  • A study evaluated 16 patients with aspergillosis (aspergilloma, allergic bronchopulmonary, and invasive forms).
  • Patients received itraconazole at 200-400 mg/day for 14-488 days.
  • Clinical, radiological, mycological, serological assessments, and drug plasma levels were monitored.

Findings:

  • Nine out of sixteen patients showed a positive response (recovery or improvement).
  • One patient did not respond to itraconazole treatment.
  • Three patients experienced relapses after initial improvement.
  • Three patients discontinued treatment due to liver function disorders, preventing full evaluation.

Implications:

  • Itraconazole demonstrates clinical efficacy in a significant proportion of aspergillosis patients.
  • The potential for relapses highlights the need for long-term management strategies.
  • Hepatotoxicity is a concern, requiring vigilant monitoring of liver function during itraconazole therapy.
  • Further research is warranted to optimize itraconazole dosing and duration for different aspergillosis types.

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