Empiric vs Preemptive Antifungal Strategy in High-Risk Neutropenic Patients on Fluconazole Prophylaxis: A Randomized Trial of the European Organization for Research and Treatment of Cancer.

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Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_E34CCCFF4BB8
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Empiric vs Preemptive Antifungal Strategy in High-Risk Neutropenic Patients on Fluconazole Prophylaxis: A Randomized Trial of the European Organization for Research and Treatment of Cancer.
Journal
Clinical infectious diseases
Author(s)
Maertens J., Lodewyck T., Donnelly J.P., Chantepie S., Robin C., Blijlevens N., Turlure P., Selleslag D., Baron F., Aoun M., Heinz W.J., Bertz H., Ráčil Z., Vandercam B., Drgona L., Coiteux V., Llorente C.C., Schaefer-Prokop C., Paesmans M., Ameye L., Meert L., Cheung K.J., Hepler D.A., Loeffler J., Barnes R., Marchetti O., Verweij P., Lamoth F., Bochud P.Y., Schwarzinger M., Cordonnier C.
Working group(s)
Infectious Diseases Group and the Acute Leukemia Group of the European Organization for Research and Treatment of Cancer
ISSN
1537-6591 (Electronic)
ISSN-L
1058-4838
Publication state
Published
Issued date
18/02/2023
Peer-reviewed
Oui
Volume
76
Number
4
Pages
674-682
Language
english
Notes
Publication types: Randomized Controlled Trial ; Journal Article
Publication Status: ppublish
Abstract
Empiric antifungal therapy is considered the standard of care for high-risk neutropenic patients with persistent fever. The impact of a preemptive, diagnostic-driven approach based on galactomannan screening and chest computed tomography scan on demand on survival and on the risk of invasive fungal disease (IFD) during the first weeks of high-risk neutropenia is unknown.
Patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) and allogeneic hematopoietic cell transplant recipients were randomly assigned to receive caspofungin empirically (arm A) or preemptively (arm B), while receiving fluconazole 400 mg daily prophylactically. The primary end point of this noninferiority study was overall survival (OS) 42 days after randomization.
Of 556 patients recruited, 549 were eligible: 275 in arm A and 274 in arm B. Eighty percent of the patients had AML or MDS requiring high-dose chemotherapy, and 93% of them were in the first induction phase. At day 42, the OS was not inferior in arm B (96.7%; 95% confidence interval [CI], 93.8%-98.3%) when compared with arm A (93.1%; 95% CI, 89.3%-95.5%). The rates of IFDs at day 84 were not significantly different, 7.7% (95% CI, 4.5%-10.8%) in arm B vs 6.6% (95% CI, 3.6%-9.5%) in arm A. The rate of patients who received caspofungin was significantly lower in arm B (27%) than in arm A (63%; P < .001).
The preemptive antifungal strategy was safe for high-risk neutropenic patients given fluconazole as prophylaxis, halving the number of patients receiving antifungals without excess mortality or IFDs. Clinical Trials Registration. NCT01288378; EudraCT 2010-020814-27.
Keywords
Humans, Antifungal Agents/therapeutic use, Fluconazole/therapeutic use, Caspofungin/therapeutic use, Mycoses/drug therapy, Hematopoietic Stem Cell Transplantation, Leukemia, Myeloid, Acute/drug therapy, Myelodysplastic Syndromes, antifungal, empiric, galactomannan, neutropenia, preemptive
Pubmed
Web of science
Open Access
Yes
Create date
25/08/2022 8:21
Last modification date
23/01/2024 8:36
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