# P-2107. Invasive fungal sinusitis in patients with hematological malignancies: a 20-year study from a tertiary academic US hospital system

**Authors:** Tejas S Athni, Carolyn Strauch, Muneerah Aleissa, Simran Gupta, Alexis Liakos, Alexandra Tong, Inia Andrea Perez Villa, Esther Arbona Haddad, Victor Kovac, Rahul S Vedula, Alice Z Maxfield, Regan Bergmark, Amy C Sherman

PMC · DOI: 10.1093/ofid/ofaf695.2271 · Open Forum Infectious Diseases · 2026-01-11

## TL;DR

This 20-year study examines invasive fungal sinusitis in patients with blood cancers, finding high mortality despite new treatments and early surgery.

## Contribution

The study provides updated insights into IFS outcomes in hematological malignancies over two decades in a US hospital system.

## Key findings

- Overall mortality was 70%, with 26.7% directly due to IFS.
- Most patients had not received antifungal prophylaxis, and Amphotericin B and voriconazole were the most common initial treatments.
- Surgery within 1 day of diagnosis was associated with lower mortality (46.7%) compared to later surgery (85.7%).

## Abstract

Invasive fungal sinusitis (IFS) can profoundly impact individuals with hematological malignancies, with high mortality rates, rapid disease progression, and slow response to medical therapy. With an evolving therapeutic landscape, outcomes for patients with heme malignancies and IFS warrant further evaluation.

We performed a single-center, retrospective review of patients with hematologic malignancies who developed proven IFS. We characterized patient demographics; oncologic history; mycologic, radiographic, and surgical data; sinonasal endoscopy findings; and mortality outcomes. Frequencies were reported for categorical variables. Medians and interquartile ranges were reported for continuous variables (R v4.3.1).

We identified 30 patients with confirmed IFS diagnosed between 2005-2024, with characteristics described in Table 1. Most patients had a diagnosis of acute myeloid leukemia (70.0%). Within 6 months prior to IFS, patients had received cytarabine (40.0%) and steroids (23.3%), with newer agents including venetoclax (33.3%), tyrosine kinase inhibitors (26.7%), brentuximab vedotin (3.3%), and tagraxofusp (3.3%). Mycologically 53% of patients had localized and 47% had disseminated fungal infection (Table 2). Histopathologic biopsy was positive in 86.7%, tissue culture in 73.3%, and PCR in 10.0% of patients. The most common fungal isolates were Aspergillus (23.3%), Mucorales (23.3%), and Fusarium (16.7%). Most patients had not received antifungal prophylaxis (93.3%). Amphotericin B (96.7%) and voriconazole (70.0%) were the most common initial treatments. Novel therapies included olorofim (3.3%) and fosmanogepix (3.3%). Half of cases were unilateral (53.3%), with further anatomical and surgical characteristics described in Table 3. Median time from IFS diagnosis to surgery was 1 day (IQR: 0-2). Overall mortality was 70.0%, with 26.7% due to IFS and median time from IFS diagnosis to death of 76 days (IQR: 21-303) (Table 4). Surgery within 1d of IFS diagnosis had 46.7% mortality, while surgery after 1d had 85.7% mortality.

Despite novel therapies and aggressive interventions, patients with IFS had high mortality. We seek to further determine specific prognostic factors that portend positive outcomes for patients with IFS.

Rahul S. Vedula, MD, NA: inventor on patent (PCT/US2020/049257) Regan Bergmark, MD MPH, Analysis Group: Advisor/Consultant|i-Mab Biopharma: Advisor/Consultant

## Linked entities

- **Chemicals:** cytarabine (PubChem CID 6253), steroids (PubChem CID 139082353), venetoclax (PubChem CID 49846579), Amphotericin B (PubChem CID 1972), voriconazole (PubChem CID 71616), olorofim (PubChem CID 91885568), fosmanogepix (PubChem CID 44123754)
- **Diseases:** acute myeloid leukemia (MONDO:0015667)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12793401/full.md

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Source: https://tomesphere.com/paper/PMC12793401