Itraconazole trough concentrations in antifungal prophylaxis with six different dosing regimens using hydroxypropyl-beta-cyclodextrin oral solution or coated-pellet capsules
A. Glasmacher et al., Itraconazole trough concentrations in antifungal prophylaxis with six different dosing regimens using hydroxypropyl-beta-cyclodextrin oral solution or coated-pellet capsules, MYCOSES, 42(11-12), 1999, pp. 591-600
We have previously shown that a trough concentration of at least 500 ng ml(
-1) itraconazole is necessary for an effective antifungal prophylaxis in ne
utropenic patients. Since the bioavailability of itraconazole is reduced in
these patients, a satisfactory dosing regimen remains to be defined. In th
is study, six dosing regimens with itraconazole capsules 400, 600 or 800 mg
day(-1) itraconazole solution 400 mg day(-1) (additional loading dose: 400
mg day(-1) solution for 2 days), 800 mg day(-1) or 400 mg day(-1) (additio
nal loading dose: 800 mg day(-1) capsules for 7 days, s/c1200) were compare
d during 160 courses of myelosuppressive chemotherapy in 123 patients with
acute leukaemia. After the first week, patients taking 800 mg day(-1) or 40
0 mg day(-1) (s/c1200) itraconazole solution achieved significantly higher
trough concentrations (high-performance liquid chromatography) than patient
s in other groups (P < 0.05) and 87 and 100%, respectively, of these had co
ncentrations > 500 ng ml(-1). Contrary to a dose of 400 mg day(-1), a dose
of 800 mg day(-1) itraconazole solution induced severe nausea and vomiting
in 46% of the patients. We conclude that 400 mg day(-1) itraconazole soluti
on with a loading dose of 800 mg day(-1) capsules for 7 days resulted in su
fficient trough concentrations from the first week onwards and appears to b
e suitable for antifungal prophylaxis in neutropenic patients.