Incidence, Patterns, and Outcomes of Fungal Infections in Patients With Graft Versus Host Disease Requiring Systemic Steroids Following Allogeneic Hematopoietic Cell Transplantation: A Systematic Review and Meta Analysis.

Transplant ProcSep 14, 2026 (epub)

Muhammad Kashif Amin, Areeba Ismail, Muhammad Shahzou Shah et al.

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In 30 seconds

This systematic review and meta-analysis pooled findings from four studies involving 1,141 patients with graft-versus-host disease (GVHD) after allogeneic hematopoietic cell transplantation who required systemic steroids. The pooled incidence of invasive fungal infections (IFIs) was 8.0% (95% CI: 6.0%-10.0%). Aspergillosis was the most frequently reported infection, with a pooled incidence of 5% (95% CI: 3.0%-9.0%). Pooled IFI-related mortality was 3% across the cohort and 39.4% among patients with established or probable IFIs. Incidence estimates varied across GVHD subgroups and prophylaxis regimens.

Key findings

  • Overall pooled IFI incidence was 8.0% (95% CI: 6.0%-10.0%; I² = 49.5%).
  • Aspergillosis had a pooled incidence of 5% (95% CI: 3.0%-9.0%; I² = 70.3%).
  • IFI incidence was 10.0% in acute GVHD and 9.0% in chronic GVHD.
  • IFI-related mortality was 3% in the full cohort and 39.4% among patients with established or probable IFIs.

Why it matters

These pooled estimates quantify the burden of IFIs in a population exposed to systemic steroids after transplantation and show that infection-related mortality remains substantial once IFI is established or probable. The findings can inform risk discussions and highlight the importance of continued attention to fungal infection prevention and recognition, while the variability between studies cautions against treating pooled estimates as precise predictions for every patient.

What to keep in mind

Only four studies were included, and several pooled estimates showed substantial heterogeneity, limiting the precision and generalisability of the results.

Source

Published in Transplant Proc. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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