Invasive Fungal Disease in Pediatric Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplant

Catherine Aftandilian1, Kenneth Weinberg, Jennifer Willert

  • 1Divisions of *Pediatric Hematology/Oncology†Stem Cell Transplantation and Regenerative Medicine‡Pediatric Infectious Diseases, Stanford University, Stanford, CA.

Insights

Invasive fungal disease (IFD) after pediatric hematopoietic stem cell transplant (HSCT) affects patients similarly regardless of prior IFD history. However, post-transplant IFD significantly increases mortality risk.

Area of Science:

  • Pediatric Hematology
  • Infectious Diseases
  • Transplantation Immunology

Background:

  • Invasive fungal disease (IFD) is a critical complication following pediatric allogeneic hematopoietic stem cell transplant (HSCT), contributing to significant morbidity and mortality.
  • Understanding IFD risk factors and outcomes in this vulnerable population is essential for improving patient survival.

Purpose of the Study:

  • To analyze the incidence and outcomes of IFD in pediatric patients undergoing allogeneic HSCT.
  • To compare IFD rates and mortality between patients with and without a history of IFD prior to HSCT.
  • To evaluate the impact of antifungal prophylaxis on post-transplant IFD rates.

Main Methods:

  • Retrospective analysis of 152 pediatric patients who underwent allogeneic HSCT between 2005 and 2012.
  • Categorization of patients based on IFD history before HSCT (n=26) and absence of IFD history (n=126).
  • Review of antifungal prophylaxis strategies and assessment of post-transplant IFD incidence and all-cause mortality.

Main Results:

  • The incidence of IFD post-HSCT was similar in patients with (7.7%) and without (7.1%) prior IFD.
  • Mortality rates did not differ significantly between patients with or without prior IFD (35% vs. 28%).
  • Patients who developed IFD post-HSCT had significantly higher all-cause mortality (67%) compared to those without post-transplant IFD (21%).

Conclusions:

  • Prior history of IFD did not significantly alter the risk of developing IFD after allogeneic HSCT in pediatric patients.
  • Post-transplant IFD is associated with a substantially increased risk of mortality.
  • Further research into identifying specific risk factors for post-transplant IFD is crucial for enhancing outcomes in pediatric HSCT recipients.

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