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Published on: July 1, 2020
Invasive fungal infections in pediatric leukemia patients receiving fluconazole prophylaxis
Zuhre Kaya1, Turkiz Gursel, Ulker Kocak
1Pediatric Hematology Unit of Department of Pediatrics, Medical School of Gazi University, Ankara, Turkey. zuhrekaya@gazi.edu.tr
Background:
Children with acute leukemia have increased risk for invasive fungal infections (IFI) but the role of long term antifungal prophylaxis (AFP) in morbidity and mortality of IFI is not well-known.
Procedure:
Medical records of 154 children with acute leukemia who received AFP with fluconazole during intensive chemotherapy were retrospectively reviewed to determine risk factors, clinical characteristics and outcome of IFI.
Results:
The overall incidence of IFI was 13.6%. Frequencies of proven, probable and possible infections were 7.2%, 2.6%, and 3.8%, respectively. The causative agent was Candida in 12 (57.2%) and Aspergillus in 9 (42.8%) children. There were 10 children with candidemia (47.6%), 7 with pulmonary aspergillosis (33.4%), 2 with hepatosplenic candidiasis (10.0%), one with sinopulmonary aspergillosis (4.5%) and one with sinus aspergillosis (4.5%). IFI was twice as common in acute myeloid leukemia (AML) (20.7%) than in acute lymphoblastic leukemia (ALL) (10.2%). Duration of profound neutropenia (P = 0.01) and steroid medications (P = 0.001) were significantly associated with IFI in univariate but not in multivariate analysis. Liposomal amphotericin B (L-AMB) was successful in 15 of 21 children as a single agent. Voriconazole produced complete response in four children with invasive aspergillosis and two with hepatosplenic candidiasis, who were unresponsive to L-AMB. The rate of IFI attributable death was 5%.
Conclusions:
Our results indicate that AFP with fluconazole and early empirical antifungal therapy may be effective in reducing the incidence and mortality of IFI in children with acute leukemia.
Insights
Long-term antifungal prophylaxis (AFP) with fluconazole may reduce invasive fungal infections (IFI) in children with acute leukemia. Early antifungal therapy also appears effective in lowering IFI incidence and mortality.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Hematology
Background:
- Children with acute leukemia face a high risk of invasive fungal infections (IFI).
- The impact of long-term antifungal prophylaxis (AFP) on IFI morbidity and mortality in this population is not well-established.
- This study investigates the role of fluconazole-based AFP in pediatric acute leukemia.
Purpose of the Study:
- To determine the risk factors, clinical characteristics, and outcomes of IFI in children with acute leukemia receiving AFP.
- To evaluate the effectiveness of fluconazole prophylaxis and early empirical antifungal therapy in managing IFI.
- To assess the incidence and mortality rates associated with IFI in this patient group.
Main Methods:
- Retrospective review of medical records for 154 children with acute leukemia undergoing intensive chemotherapy with fluconazole AFP.
- Analysis of IFI incidence, causative agents (Candida, Aspergillus), and specific infection types (candidemia, aspergillosis).
- Evaluation of risk factors including neutropenia and steroid use, and treatment outcomes with Liposomal amphotericin B and Voriconazole.
Main Results:
- The overall incidence of IFI was 13.6%, with Candida and Aspergillus as primary pathogens.
- IFI was more common in acute myeloid leukemia (AML) than acute lymphoblastic leukemia (ALL).
- Profound neutropenia and steroid use were associated with IFI; 5% of deaths were attributable to IFI.
Conclusions:
- Antifungal prophylaxis with fluconazole and early empirical antifungal treatment may effectively reduce IFI incidence and mortality in pediatric acute leukemia.
- Liposomal amphotericin B and Voriconazole showed success in treating various fungal infections.
- Further research into optimal antifungal strategies for immunocompromised pediatric patients is warranted.
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