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Antifungal prophylaxis with micafungin in patients treated for childhood cancer
Shigenori Kusuki1, Yoshiko Hashii, Hisao Yoshida
1Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan.
Background:
Invasive fungal infections (IFIs) remain a major cause of infectious morality in neutropenic patients receiving chemotherapy or hematopoietic stem cell transplantation (HSCT). Micafungin exhibits broad antifungal activity against both Aspergillus and Candida species. We performed a retrospective study to determine the efficacy and safety of prophylactic micafungin against IFI in pediatric neutropenic patients during chemotherapy or HSCT.
Procedure:
Forty patients were given micafungin (3 mg/kg/day) intravenously for neutropenia: 131 patient-cycles (39 patients) after chemotherapy and 15 patient-cycles (14 patients) after HSCT. Median duration of neutropenia and micafungin prophylaxis was 13 and 23 days after chemotherapy and HSCT, respectively.
Results:
Treatment success rate, defined as absence of proven, probable, possible, or suspected IFIs, was 93.9% (121/131) and 80.0% (12/15) for chemotherapy and HSCT, respectively. Proven or probable IFI was documented in only one patient after HSCT. No adverse events were observed that could be related to micafungin prophylaxis.
Conclusions:
These results suggest that prophylactic micafungin is well tolerated and may prevent IFIs in pediatric patients with neutropenia receiving chemotherapy or HSCT.
Insights
Prophylactic micafungin effectively prevented invasive fungal infections (IFIs) in pediatric patients undergoing chemotherapy or hematopoietic stem cell transplantation (HSCT). This antifungal agent demonstrated good tolerability and safety in neutropenic children.
Area of Science:
- Mycology
- Pediatric Oncology
- Hematology
Background:
- Invasive fungal infections (IFIs) are a significant cause of mortality in neutropenic patients undergoing chemotherapy or hematopoietic stem cell transplantation (HSCT).
- Micafungin possesses broad-spectrum antifungal activity against Aspergillus and Candida species, making it a potential prophylactic agent.
- Pediatric neutropenic patients undergoing chemotherapy or HSCT are at high risk for IFIs.
Purpose of the Study:
- To evaluate the efficacy of prophylactic micafungin in preventing IFIs.
- To assess the safety and tolerability of micafungin prophylaxis in pediatric neutropenic patients.
- To determine the treatment success rate of micafungin in preventing IFIs during chemotherapy and HSCT.
Main Methods:
- Retrospective study of 40 pediatric patients receiving micafungin (3 mg/kg/day) intravenously.
- Analysis of 131 patient-cycles post-chemotherapy and 15 patient-cycles post-HSCT.
- Median neutropenia and prophylaxis duration of 13 days (chemotherapy) and 23 days (HSCT).
Main Results:
- High treatment success rates observed: 93.9% after chemotherapy and 80.0% after HSCT.
- Only one case of proven or probable IFI documented, occurring after HSCT.
- No adverse events were attributed to micafungin prophylaxis, indicating good tolerability.
Conclusions:
- Prophylactic micafungin appears to be a safe and well-tolerated option for preventing IFIs in pediatric neutropenic patients.
- Micafungin demonstrates potential efficacy in reducing the incidence of IFIs in this vulnerable patient population.
- Further prospective studies may be warranted to confirm these findings.
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