Abstract |
Antifungal prophylaxis during first remission induction chemotherapy for acute myelogenous leukaemia requires broad spectrum azoles. In a clinical trial, therapeutic drug monitoring (TDM) of antifungal prophylaxis with voriconazole 200 mg bid was evaluated in a population of six patients. High pressure liquid chromatography was applied. Trough levels were obtained 24 h after the last voriconazole dose. Median time of voriconazole exposure prior to sample acquisition was 16 days (range 9-21). The mean voriconazole concentration was 486 μg l(-1) and ranged from 136 μg l(-1) to 1257 μg l(-1). Among possible or probable treatment-related adverse events, elevated liver function tests were the most frequent. Five of six patients developed fever during neutropenia, but none of them developed pulmonary infiltrates or other signs of invasive fungal infection while on voriconazole prophylaxis. Future investigations might aim at identifying drug level thresholds that allow for minimum toxicity and optimum efficacy of antifungal prophylaxis.
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Authors | Maria J G T Rüping, Carsten Müller, Jörg J Vehreschild, Angelika Böhme, Sabine Mousset, Urs Harnischmacher, Peter Frommolt, Gernot Wassmer, Ivonne Drzisga, Michael Hallek, Oliver A Cornely |
Journal | Mycoses
(Mycoses)
Vol. 54
Issue 3
Pg. 230-3
(May 2011)
ISSN: 1439-0507 [Electronic] Germany |
PMID | 19889174
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2009 Blackwell Verlag GmbH. |
Chemical References |
- Antifungal Agents
- Pyrimidines
- Triazoles
- Voriconazole
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Topics |
- Adolescent
- Aged
- Antifungal Agents
(administration & dosage, pharmacokinetics)
- Chemoprevention
(methods)
- Drug Monitoring
(methods)
- Female
- Humans
- Leukemia, Myeloid
(complications)
- Male
- Middle Aged
- Mycoses
(prevention & control)
- Pyrimidines
(administration & dosage, pharmacokinetics)
- Serum
(chemistry)
- Triazoles
(administration & dosage, pharmacokinetics)
- Voriconazole
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