An update on pharmacotherapy for fungal infections in allogeneic stem cell transplant recipients

Paraskevi Panagopoulou1, Emmanuel Roilides2

  • 1Pediatric Hematology & Oncology, 4th Department of Pediatrics, Aristotle University School of Medicine and Papageorgiou General Hospital, Thessaloniki, Greece.

PubMed
Abstract

Insights

Invasive fungal diseases (IFD) are a major risk for hematopoietic stem cell transplantation (HSCT) patients. This review details IFD prophylaxis and treatment strategies, including current antifungal options and recommendations for HSCT recipients.

Area of Science:

  • Hematology
  • Infectious Diseases
  • Mycology

Background:

  • Invasive fungal diseases (IFD) are a significant cause of morbidity and mortality in hematopoietic stem cell transplantation (HSCT) recipients.
  • Effective management of IFD requires understanding local epidemiology, risk factors, and current treatment guidelines.

Purpose of the Study:

  • To provide a comprehensive overview of the epidemiology, causes, and risk factors of IFD in allogeneic HSCT.
  • To discuss current prophylaxis and treatment strategies for IFD across different phases of HSCT.
  • To present recent data on antifungal agents, including formulations, dosing, safety, efficacy, and therapeutic drug monitoring, along with updated recommendations.

Main Methods:

  • A literature search was conducted in PubMed, Scopus, and clinicaltrials.gov.
  • The search focused on studies published between January 2014 and April 2024.
  • The review synthesizes information on IFD epidemiology, risk factors, prophylaxis, and treatment in HSCT recipients.

Main Results:

  • Antifungal prophylaxis and therapy selection should be guided by local IFD epidemiology.
  • Fluconazole is recommended for prophylaxis before engraftment against Candida spp.; mold-active agents are preferred post-engraftment.
  • First-line treatments include echinocandins for candidiasis, mold-active azoles or liposomal amphotericin B (L-AmB) for aspergillosis, and L-AmB or isavuconazole for mucormycosis.

Conclusions:

  • Optimizing diagnostic tools for prompt and accurate IFD detection is crucial to minimize antifungal exposure, drug interactions, and costs.
  • Further research is needed to refine treatments for resistant or refractory fungal strains in HSCT patients.
  • The choice between empirical (fever-driven) and diagnostic-driven treatment strategies for IFD remains an area for further investigation.