This real-world observational study aims to evaluate the effectiveness, safety, and therapeutic drug monitoring (TDM) of liposomal amphotericin B (L-AmB) in solid organ transplant recipients with invasive fungal disease (IFD). IFD is a major cause of morbidity and mortality in transplant recipients because of long-term immunosuppressive therapy and increased susceptibility to opportunistic fungal infections. This is a single-center ambispective cohort study conducted at Sichuan Provincial People's Hospital. The study includes a prospective cohort of solid organ transplant recipients receiving L-AmB therapy and a historical control cohort treated with alternative systemic antifungal regimens. Clinical management and treatment decisions will be determined by treating physicians according to routine clinical practice, and no study-specific intervention will be introduced. The study will collect information on demographic characteristics, transplant type, immunosuppressive regimens, fungal pathogens, infection sites, antifungal treatment strategies, laboratory findings, and clinical outcomes. Particular attention will be given to renal safety, electrolyte abnormalities, and therapeutic drug monitoring of liposomal amphotericin B. Plasma concentrations of L-AmB, treatment modifications, temporary treatment discontinuation, and concentration-related safety and effectiveness outcomes will be recorded during antifungal therapy. The primary outcomes are the 28-day clinical response rate and 84-day all-cause mortality. Secondary outcomes include mycological clearance, acute kidney injury, electrolyte abnormalities, breakthrough fungal infection, treatment discontinuation due to adverse events, liposomal amphotericin B plasma concentrations, and the associations between L-AmB exposure and clinical outcomes or treatment-related toxicities. The study is expected to provide real-world evidence regarding the effectiveness, safety, and pharmacokinetic characteristics of L-AmB in transplant recipients, support optimization of antifungal treatment strategies, and inform individualized dosing and monitoring approaches in this high-risk population.
Study Type
OBSERVATIONAL
Enrollment
120
Liposomal amphotericin B administered for treatment of proven, probable, or possible invasive fungal disease in solid organ transplant recipients according to routine clinical practice. Dose adjustment and treatment duration are determined by treating physicians.
Alternative systemic antifungal agents including azoles, echinocandins, or other standard antifungal therapies administered according to routine clinical practice in historical control patients with invasive fungal disease.
Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital
Chengdu, Sichuan, China
28-Day Clinical Response Rate
Proportion of participants achieving complete or partial clinical response at Day 28 after initiation of antifungal therapy.
Time frame: Day 28
84-Day All-Cause Mortality
All-cause mortality occurring within 84 days after initiation of antifungal therapy.
Time frame: Day 84
Mycological Clearance Rate
Proportion of participants with documented clearance of fungal pathogens.
Time frame: Day 28
Acute Kidney Injury
Occurrence of acute kidney injury during antifungal treatment.
Time frame: Baseline through Day 84
Electrolyte Abnormalities
Occurrence of hypokalemia, hypomagnesemia, or other treatment-related electrolyte disturbances.
Time frame: Baseline through Day 84
Liposomal Amphotericin B Plasma Concentration
Plasma concentration of liposomal amphotericin B measured during antifungal therapy.
Time frame: Baseline through Day 84
Association Between Liposomal Amphotericin B Exposure and Clinical Response
Relationship between liposomal amphotericin B plasma concentration and clinical response.
Time frame: Baseline through Day 84
Association Between Liposomal Amphotericin B Exposure and Adverse Events
Relationship between liposomal amphotericin B plasma concentration and treatment-related adverse events, including nephrotoxicity and electrolyte abnormalities.
Time frame: Baseline through Day 84
Breakthrough Fungal Infection
Occurrence of breakthrough invasive fungal infection during antifungal therapy.
Time frame: Baseline through Day 84
Antifungal Treatment Discontinuation Due to Adverse Events
Permanent discontinuation of antifungal therapy because of treatment-related adverse events.
Time frame: Baseline through Day 84
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.