What is the recommended dose of liposomal (Liposomal) amphotericin B for pulmonary mucormycosis?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 13, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Recommended Dose of Liposomal Amphotericin B for Pulmonary Mucormycosis

For pulmonary mucormycosis, liposomal amphotericin B should be administered at a dose of 5-10 mg/kg/day as first-line treatment. 1

Dosing Recommendations

  • Liposomal amphotericin B (L-AmB) is the drug of choice for treating pulmonary mucormycosis with strong evidence supporting its use 1
  • The recommended dose should be at least 5 mg/kg/day, with doses ranging from 5-10 mg/kg/day depending on disease severity 1
  • The full daily dose should be given from the first treatment day rather than slowly increasing over several days 1
  • For pulmonary mucormycosis without CNS involvement, 5 mg/kg/day may be sufficient 1
  • Higher doses (10 mg/kg/day) should be considered for severe infections or when there is CNS involvement 1

Evidence for Dosing

  • Multiple guidelines consistently recommend a minimum dose of 5 mg/kg/day for pulmonary mucormycosis 1
  • Case series have shown that recipients of increased doses (up to 10 mg/kg/day) tended to have increased response rates 1
  • A prospective pilot study using high-dose L-AmB (10 mg/kg/day) for mucormycosis showed an overall response rate of 36% at week 4 and 45% at week 12 2
  • Doses higher than 10 mg/kg/day have not been shown to result in higher blood concentrations and are not recommended 1

Renal Toxicity Considerations

  • Patients receiving 10 mg/kg/day may experience substantial serum creatinine increases, though these are mostly reversible 1
  • If substantial renal toxicity develops, the dose can be reduced, but doses below 5 mg/kg/day are only marginally recommended 1
  • In a prospective study of high-dose L-AmB (10 mg/kg/day), serum creatinine doubled in 40% of patients but returned to normal levels within 12 weeks in 63% of those affected 2

Treatment Duration and Approach

  • Treatment should be initiated immediately upon suspicion of mucormycosis in immunocompromised patients 1
  • Surgical resection or debridement should be combined with antifungal therapy whenever possible 1
  • The optimal length of treatment has not been clearly defined but typically continues until clinical and radiological resolution of infection 1
  • Treatment delays of 6 or more days from symptom onset have been associated with doubled mortality rates 1

Alternative Formulations

  • Amphotericin B lipid complex (ABLC) at 5 mg/kg/day can be considered for patients without CNS involvement, with moderate strength of recommendation 1
  • Conventional amphotericin B deoxycholate is discouraged due to its substantial toxicity, especially at the doses needed for mucormycosis 1

Combination Therapy

  • Limited data support combinations of L-AmB with azoles or echinocandins 1
  • Recent research suggests that combination of L-AmB and isavuconazole may have synergistic effects in experimental models 3
  • However, clinical evidence for combination therapy remains limited and is only marginally recommended 1

Special Considerations

  • In patients with renal impairment, L-AmB is preferred over conventional amphotericin B formulations 1
  • For patients who cannot tolerate or have contraindications to L-AmB, isavuconazole can be considered as an alternative first-line treatment with moderate strength of recommendation 1
  • Adjunctive nebulized amphotericin B has been studied but has not shown significant improvement in treatment outcomes 4, 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.