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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Maertens Johan, Lodewyck Tom, Donnelly J Peter, Chantepie Sylvain, Robin Christine, Blijlevens Nicole, Turlure Pascal, Selleslag Dominik, Baron Frédéric, Aoun Mickael, Heinz Werner J, Bertz Hartmut, Ráčil Zdeněk, Vandercam Bernard, Drgona Lubos, Coiteux Valerie, Llorente Cristina Castilla, Schaefer-Prokop Cornelia, Paesmans Marianne, Ameye Lieveke, Meert Liv, Cheung Kin Jip, Hepler Deborah A, Loeffler Jürgen, Barnes Rosemary, Marchetti Oscar, Verweij Paul, Lamoth Frederic, Bochud Pierre-Yves, Schwarzinger Michael, Cordonnier Catherine, Infectious Diseases Group and the Acute Leukemia Group of the European Organization for Research and Treatment of Cancer
Аннотация
METHODS: 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.
RESULTS: 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).
CONCLUSIONS: 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.