Voriconazole

Background

• Azole antifungal derived from fluconazole to improve mold coverage
• Indications include Alternaria, Blastomyces dermatitidis, Coccidioides immitis, Exophiala, Exserohilum, Fungal endocarditis, Histoplasma capsulatum, Rasamsonia

Mechanism of Action

• Like all azoles, inhibits Erg11/Cyp51p lanosterol 14-α-demethylase in the ergosterol synthesis pathway

Pharmacokinetics and Pharmacodynamics

• Non-linear pharmacokinetics
• 58% protein-bound
• CSF 50% of plasma concentration
• Less than 5% excreted unchanged in the urine

Spectrum of Activity

• Active against Aspergillus (including Aspergillus terreus), Scedosporium species, Fusarium species, and Candida species
• Possibly active against Cryptococcus species, Blastomyces dermatitidis, Coccidioides immitis, and Histoplasma capsulatum
• Less active against Sporothrix schenckii

Breakpoints

Species	ECV (μg/mL)	Breakpoints (μg/mL)				Breakpoints (mm)
		S	I	SDD	R	S	I	SDD	R
Candida albicans	0.3	≤0.12	0.25-0.5	—	≥1	≥17	15-16	—	≤14
Candida glabrata	0.25	—	—	—	—	—	—	—	—
Candida krusei	0.5	≤0.5	1	—	≥2	≥15	13-14	—	≤12
Candida parapsilosis	0.03	≤0.12	0.25-0.5	—	≥1	≥17	15-16	—	≤14
Candida tropicalis	0.12	≤0.12	0.25-0.5	—	≥1	≥17	15-16	—	≤14
Cryptococcus neoformans	0.25
Cryptococcus gattii	0.5
Aspergillus flavus	2
Aspergillus fumigatus	1
Aspergillus niger	2
Aspergillus terreus	2

Dosing

• Voriconazole 6 mg/kg IV q12h x2 followed by 3-4 mg/kg PO/IV q12h

Therapeutic Drug Monitoring

• Measure trough within 7 days of starting, and at regular intervals or following dose adjustment
• Target trough > 1 mg/L for prophylaxis and treatment

Trough (mcg/mL)	Recommendation
0.0 to 0.6	Increase dose by 100 mg and recheck trough on day 5 of new regimen
0.7 to 0.9	Increase dose by 50 mg and recheck trough on day 5 of new regimen
1.0 to 4.0	At target, no dose adjustment needed
4.1 to 5.5	Decrease dose by 50 mg and recheck trough on day 5 of new regimen
5.6 to 7.9	Hold dose. Follow daily trough levels, then restart when trough is ≤2.5 at a dose decreased by 100 mg. Recheck trough on day 5 of new regimen.
≥8.0	Hold dose. Follow daily trough levels, then restart when trough is ≤2.5 at a dose decreased by 50%. Recheck trough level on day 5 of new regimen.

Safety

• Elevated levels predict neurotoxicity, but not hepatotoxicity

Adverse Drug Reactions

• Visual, which tend to improve after the first week of therapy and are reversible
  • Floaters (photopsia) that usually improves with time (30%)
  • Visual hallucinations (5%)
  • Colour vision loss, blurred vision, photophobia
• Dermatologic
  • Rashes, usually mild
  • Stevens-Johnson syndrome and toxic epidermal necrolysis (rare)
  • Photosensitivity
• Hepatotoxicity, proportional to serum levels
• QTc prolongation
• Headache, nausea and vomiting, diarrhea, abdominal pain

Drug-Drug Interactions

• Voriconazole is metabolised by CYP450 enzymes
• Voriconazole also inhibits CYP3A4 and CYP2C9

Drug	Recommendation
Decreases voriconazole levels
carbamazepine	contraindicated
long-acting barbiturates	contraindicated
rifampin	contraindicated
Levels increased by voriconazole
astemizole	contraindicated
cisapride	contraindicated
cyclosporine	reduce cyclosporine dosage 50% and monitor levels
ergot alkaloids	contraindicated
omeprazole	reduce omeprazole by 50%
quinidine	contraindicated
sirolimus	contraindicated
tacrolimus	reduce tacrolimus levels to 33% and monitor levels
terfenadine	contraindicated
warfarin	monitor INR
Decreases voriconazole levels, and levels increased by voriconazole
rifabutin	contraindicated
phenytoin	double voriconazole, and monitor phenytoin levels
Levels likely increased by voriconazole
sulfonylureas	monitor for side effects of drug and consider decreasing dosage
statins
vinca alkaloids
calcium channel blockers
benzodiazepines

Further Reading

• Voriconazole Dose Modification Guideline to Optimize Therapeutic Levels in Patients With Hematologic Malignancies. Open Forum Infect Dis. 2015;2(S1):810. doi: 10.1093/ofid/ofv133.527