# Influence of Extended Itraconazole Antifungal Prophylaxis on the Development of Fungal Infections After Lung Transplant

**Authors:** Sabrina Fischer, Raksha Patel, Mufaddal Mamawala, Susan K. Mathai, Katherine Vandervest, Tiana Endicott-Yazdani, Chetan Naik, Todd Grazia, Lisa Fuller

PMC · DOI: 10.1155/joot/6995822 · Journal of Transplantation · 2026-02-26

## TL;DR

Long-term itraconazole is better than short-term inhaled amphotericin at preventing fungal infections after lung transplants and is better tolerated.

## Contribution

Demonstrates that extended itraconazole prophylaxis reduces fungal infections and improves tolerability compared to short-term inhaled amphotericin in lung transplant patients.

## Key findings

- Itraconazole group had a significantly lower incidence of invasive fungal infections (56.8%) compared to the amphotericin group (76.9%).
- Itraconazole was associated with fewer positive fungal cultures for Aspergillus spp., Penicillium spp., and yeast.
- Amphotericin group had higher discontinuation rates due to intolerance (12%) compared to itraconazole (3.2%).

## Abstract

Invasive fungal infections (IFIs) are associated with a high mortality in lung transplant recipients, with no consensus on optimal antifungal prophylaxis. We aimed to assess the efficacy of long‐term itraconazole compared to short‐term inhaled amphotericin to prevent IFIs post‐transplant.

A retrospective review of adult lung transplant recipients from January 2016 to September 2022 was conducted. The cohort was divided into two groups based on initial mold prophylaxis: long‐term itraconazole and short‐term inhaled amphotericin. The primary outcome was the incidence of IFIs. The secondary outcomes included the time to IFI, incidence of fungal species found on cultures, and safety/tolerability.

A total of 203 patients met the inclusion criteria (amphotericin group n = 108, itraconazole group n = 95). The overall incidence of IFIs was significantly higher in the amphotericin group than the itraconazole group (76.9% vs. 56.8%, p = 0.002). The Kaplan–Meier curve for the risk of IFI within 1 year of transplant showed a shorter time to IFI in the amphotericin group (p = 0.009). In the amphotericin group, there was an increased incidence of positive fungal cultures compared to the itraconazole group with Aspergillus spp. (25% vs. 8.4%, p = 0.002), Penicillium spp. (25.9% vs. 9.5%, p = 0.002), yeast (70.4% vs. 36.8%, p ≤ 0.001), and other positive fungal cultures (28.7% vs. 12.6%, respectively, p = 0.005). The amphotericin group had more discontinuations due to intolerance than the itraconazole group (12% vs. 3.2%, p = 0.019).

In adult lung transplant recipients, long‐term prophylaxis with itraconazole was more effective at preventing overall IFIs, positive cultures with Aspergillus spp., and was better tolerated than short‐term inhaled amphotericin.

## Linked entities

- **Chemicals:** itraconazole (PubChem CID 55283), amphotericin (PubChem CID 5280965)

## Full-text entities

- **Genes:** CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}
- **Diseases:** toxicity (MESH:D064420), cystic fibrosis (MESH:D003550), infection (MESH:D007239), Cancer (MESH:D009369), ischemic injury (MESH:D017202), lung diseases (MESH:D008171), death (MESH:D003643), PAH (MESH:D000081029), bronchiectasis (MESH:D001987), viral infections (MESH:D014777), PJP (MESH:D011020), colonization (MESH:D003108), Infectious Diseases (MESH:D003141), Fungal Infections (MESH:D009181), Aspergillosis (MESH:D001228), IFIs (MESH:D000072742), necrotic (MESH:D009336), bronchospasm (MESH:D001986), ILD (MESH:D017563), COPD (MESH:D029424), nausea (MESH:D009325), hypogammaglobulinemia (MESH:D000361), heart failure (MESH:D006333)
- **Chemicals:** ivacaftor (MESH:C545203), azole (MESH:D001393), Basiliximab (MESH:D000077552), Amphotericin (MESH:D000666), isavuconazole (MESH:C508735), bilirubin (MESH:D001663), elexacaftor (MESH:C000629074), tacrolimus (MESH:D016559), SUBA (-), mycophenolate mofetil (MESH:D009173), voriconazole (MESH:D065819), creatinine (MESH:D003404), tezacaftor (MESH:C000625213), posaconazole (MESH:C101425), nystatin (MESH:D009761), fluconazole (MESH:D015725), triazole (MESH:D014230), Itraconazole (MESH:D017964), prednisone (MESH:D011241)
- **Species:** Homo sapiens (human, species) [taxon 9606], Candida [taxon 1535326], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Aspergillus flavus (species) [taxon 5059], Aspergillus fumigatus (species) [taxon 746128]

## Full text

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## Figures

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## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938488/full.md

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Source: https://tomesphere.com/paper/PMC12938488