Comparative efficacy of antifungal prophylaxis in acute myeloid leukemia: A systematic review and meta-analysis.

C Cameron Hunter (6University of Pittsburgh Medical Center, Medicine, Pittsburgh, United States) A Abdulrahman Alhajahjeh (2University of Jordan School of Medicine, Amman, Jordan) N Niroop Rajashekar (Yale School of Medicine and Yale Cancer Center, New Haven, CT) A Alyssa Grimshaw (4Yale University, Harvey Cushing/John Hay Whitney Medical Library, New Haven, United States) A Andrew Chou H Heidi Roeder (Yale New Haven Hospital, Smilow Cancer Center, New Haven, CT) W William Eighmy (Yale New Haven Hospital, Smilow Cancer Center, New Haven, CT) L Lourdes Mendez (4Yale University, New Haven, United States) M Maximilian Stahl N Nikolai Alexandrovich Podoltsev (Yale School of Medicine, New Haven, CT) A Amer Methqal Zeidan (Yale School of Medicine, New Haven, CT) R Rory Shallis (1H. Lee Moffitt Cancer Center, Tampa, United States) J Jan Philipp Bewersdorf

Abstract

e18515 Background: Acute myeloid leukemia (AML) is characterized by prolonged neutropenia and a high risk of infections, including invasive fungal infections (IFI), which are associated with substantial mortality rates of 40–70%. To mitigate this risk, antifungal prophylaxis (AFP) is often used. Current guidelines recommend posaconazole (PCZ) as the agent with the most robust data (Pagano et al. Leukemia 2025), but factors including cost, toxicities, and drug-drug interactions (DDIs) complicate use of common AFP agents, with a dearth of literature directly comparing them. Methods: We conducted a systematic review comparing IFI rate and AFP use in adult and pediatric patients with AML. In total, 2,994 records were identified, of which 367 underwent full-text review. Ultimately, 138 studies were analyzed. 81 studies reported rates of possible, probable, and proven (PsPbPv) IFI while 132 studies reported rates of probable and proven (PbPv) IFI. Patients received intensive therapy (n=78, 57%), less-intensive therapy (n=15, 11%), or both (n=25, 18%). Some (n=20, 14%) studies did not record therapy intensity. A mixed-effects model with PCZ IFI rate as reference/intercept was used. Results: When evaluating the rate of PsPbPv IFI (k=135), first-generation azoles (21.0%, p=0.027) and no AFP (29.2%, p<0.0001) were significantly higher than PCZ (15.3%). Limiting to PbPv IFI rate (k=226), first-generation azoles (9.6%, p<0.0001), amphotericin B (13.2%, p=0.0009), isavuconazole (8.8%, p=0.033), and no AFP (10.7%, p<0.0001) were significantly higher than PCZ (5.0%). IFI rate with voriconazole and echinocandin prophylaxis was not significantly different than PCZ. Subgroup meta-analysis of less-intensive patients was underpowered to detect any difference aside from a higher rate of PsPbPv IFI for first-generation azoles (20.8%, p=0.030) compared to PCZ (9.4%). Conclusions: Our study is the first comparative systematic review of all primary AFP strategies in patients with AML, with considerable dataset of 25,431 patients across 138 studies, the majority with data for patients on intensive therapy (74.6%). Results suggest that echinocandins and second-generation azoles offer comparable protection against PsPbPv IFI. Given the factors complicating the use of these agents including toxicities, DDIs, and no oral formulations, further prospective studies are imperative for further comparison. PsPbPv IFI [95% CI] p-value PbPv IFI [95% CI] p-value Posaconazole 15.3% [12.6-18.5%] --ref-- 5.0% [4.2-6.0%] --ref-- Voriconazole 14.3% [10.4-19.3%] 0.703 5.7% [4.2-7.5%] 0.489 Isavuconazole 15.1% [8.0-26.8%] 0.966 8.8% [5.4-13.9%] 0.033 First-gen azoles 21.0% [17.1-25.6%] 0.027 9.6% [8.0-11.5%] <0.0001 Echinocandins 14.0% [8.4-22.5%] 0.734 7.0% [4.6-10.5%] 0.161 Amphotericin B 28.9% [15.2-47.9%] 0.062 13.2% [7.7-21.5%] 0.0009 No AFP 29.2% [23.0-36.4%] <0.0001 10.7% [8.5%-13.4%] <0.0001

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (13)

C

Cameron Hunter

6University of Pittsburgh Medical Center, Medicine, Pittsburgh, United States

A

Abdulrahman Alhajahjeh

2University of Jordan School of Medicine, Amman, Jordan

N

Niroop Rajashekar

Yale School of Medicine and Yale Cancer Center, New Haven, CT

A

Alyssa Grimshaw

4Yale University, Harvey Cushing/John Hay Whitney Medical Library, New Haven, United States

A

Andrew Chou

H

Heidi Roeder

Yale New Haven Hospital, Smilow Cancer Center, New Haven, CT

W

William Eighmy

Yale New Haven Hospital, Smilow Cancer Center, New Haven, CT

L

Lourdes Mendez

4Yale University, New Haven, United States

M

Maximilian Stahl

N

Nikolai Alexandrovich Podoltsev

Yale School of Medicine, New Haven, CT

A

Amer Methqal Zeidan

Yale School of Medicine, New Haven, CT

R

Rory Shallis

1H. Lee Moffitt Cancer Center, Tampa, United States

J

Jan Philipp Bewersdorf