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Tables for:
Invasive Fungal Infections in the Neutropenic Cancer Patient: Current Approaches and Future Strategies

[Infect Med 19(7):326-334, 2002. © 2002 Cliggott Publishing, Division of SCP Communications ]


Table 1. Chemotherapy for invasive infections by opportunistic yeasts


Fungal diseaseDrug and dosage
Invasive candidiasis
   Uncomplicated fungemiaAmphotericin B desoxycholate (D-AmB), 0.5 - 1 mg/kg/d
Fluconazole,* 400 - 800 mg/d
   Acute single site or disseminated
   candidiasis ± fungemia
D-AmB, 0.5 - 1 mg/kg/d ± 5-fluorocytosine (5-FC), 100 mg/kg/d Fluconazole,* 400 - 800 mg/d
Amphotericin B lipid formulations, 5 mg/kg/d starting dosage
Echinocandin-lipopeptides (investigational)
Second-generation triazoles (investigational)
Trichosporon and Blastoschizomyces infectionFluconazole,* 400 - 800 mg/d ± D-AmB, >/= 1 mg/kg/d
Second-generation triazoles (investigational)
CryptococcosisD-AmB, 0.7 mg/kg/d + 5-FC, 100 mg/kg/d for a minimum of 2 weeks (induction), followed in stable patients by fluconazole,* 400 mg/d, for consolidation and maintenance
Liposomal amphotericin B, 5 mg/kg/d§
Other rare yeast infections (eg, Rhodotorula rubra, Hansenula anomala, Saccharomyces cerevisiae)D-AmB, 0.5 - 1 mg/kg/d ± 5-FC,‡ 100 mg/kg/d
Fluconazole,* 400 - 800 mg/d

*Loading dose: twice the target dose on the first day of treatment. Dosage adjustment may be required with reduced creatinine clearance and high dosages.
Only for identified and in vitro-susceptible isolates.
Monitoring of serum levels required (< 100 µg/mL; target, 40 - 60 µg/mL). Dosage adjustment with reduced creatinine clearance.
§For patients who cannot tolerate D-AmB or who have infections refractory to D-AmB.


Table 2. Chemotherapy for invasive infections by opportunistic molds


Causative organismChemotherapy
Aspergillus fumigatus
Aspergillus flavus
Aspergillus niger
Aspergillus terreus
Amphotericin B desoxycholate (D-AmB), 1 - 1.5 mg/kg/d
Voriconazole,* 4 mg/kg bid
Amphotericin B lipid formulations, 5 mg/kg/d starting dosage
Itraconazole,§ 200 - 600 mg/d
Caspofungin,|| 50 mg/d
Second-generation antifungal triazoles (investigational)
Fusarium solani
Fusarium oxysporum
Fusarium moniliforme
Acremonium species
Paecilomyces lilacinus
Paecilomyces variotii
Pseudallescheria boydii
Scedosporium apiospermum
Scedosporium prolificans
D-AmB, 1 - 1.5 mg/kg/d
Amphotericin B lipid formulations, 5 mg/kg/d starting dosage
Itraconazole,§ 200 - 600 mg/d (only for second-line therapy for P variotii, P boydii, and S apiospermum infections)
Second-generation antifungal triazoles (investigational)
S prolificans: consider high-dose lipid-based amphotericin B or combination of itraconazole and terbinafine
Pigmented molds
   Bipolaris
   Exophiala
   Alternaria and others
 
D-AmB, 1 - 1.5 mg/kg/d ± 5-fluorocytosine, 100 mg/kg/d or
Lipid formulations of amphotericin B, 5 mg/kg/d starting dosage or
Itraconazole,§ 200 - 600 mg/d or
Second-generation antifungal triazoles (investigational)
Zygomycetes
   Rhizopus species
   Mucor species
   Absidia species
 
D-AmB, 1 - 1.5 mg/kg/d
Lipid formulations of amphotericin B, 5 mg/kg/d starting dosage
Endemic molds
   Histoplasma capsulatum
   Blastomyces dermatitidis
   Coccidioides immitis
 
D-AmB, 0.5 - 1 mg/kg/d
Itraconazole,§ 200 - 400 mg/d, for H capsulatum and B dermatitidis
Fluconazole,# 400 - 800 mg/d, for C immitis

*A recently published, open, randomized trial has demonstrated superior response rates and improved survival at week 12 of therapy with voriconazole (6 mg/kg IV for 2 doses, followed by 4 mg/kg IV q12h with option to switch to 200 mg PO bid) in comparison with D-AmB (1 mg/kg/d). Approval of this indication by the FDA was pending at the time of the preparation of this article.
For patients who cannot tolerate or who have infections refractory to D-AmB.
For maintenance in stable patients.
§Monitoring of serum levels recommended (> 0.5 µg/mL [high-performance liquid chromatography] or > 2 µg/mL [bioassay] at trough. Loading dose: 200 mg tid over 3 days. Maximum: 600 mg/d. IV therapy: 200 mg bid over 2 days, followed by 200 mg/d (maximum: 14 days).
||In patients who cannot tolerate or who have infections refractory to standard therapy; loading dose: 70 mg on day 1 of therapy.
Monitoring of serum levels required (< 100 µg/mL; target, 40 - 60 µg/mL). Dosage adjustment with reduced creatinine clearance.
#Loading dose: twice the target dose on the first day of treatment. Dosage adjustment may be required with reduced creatinine clearance and high dosages.