Literature DB >> 29746955

Micafungin versus posaconazole prophylaxis in acute leukemia or myelodysplastic syndrome: A randomized study.

David J Epstein1, Susan K Seo2, Yao-Ting Huang1, Jay H Park3, Virginia M Klimek3, Ellin Berman3, Martin S Tallman3, Mark G Frattini3, Genovefa A Papanicolaou4.   

Abstract

OBJECTIVES: To compare the effectiveness and tolerability of micafungin versus posaconazole during chemotherapy-induced neutropenia in acute leukemia (AL) and myelodysplastic syndrome (MDS).
METHODS: Patients with AL or MDS undergoing chemotherapy were randomized to open-label micafungin 100 mg intravenously daily or posaconazole suspension 400 mg orally twice daily until neutrophil recovery, up to 28 days. Patients were followed for 12 weeks. The primary endpoint was prophylaxis failure (premature discontinuation due to infection, intolerance, adverse event, or death). Time to failure and survival were calculated by Kaplan-Meier analysis.
RESULTS: From March 2011 to May 2016, 113 patients who received at least 2 doses of prophylaxis were analyzed (58 patients randomized to micafungin and 55 to posaconazole). Prophylaxis failure occurred in 34.5% and 52.7% of patients on micafungin and posaconazole, respectively (P = 0.0118). The median number of days on prophylaxis was 16 [interquartile range (IQR) 12-20] for micafungin and 13 [IQR 6-16] for posaconazole (P = 0.01). Micafungin failures were largely due to antifungal treatment; posaconazole failures were mostly due to gastrointestinal intolerance or adverse effects. IFI incidence and survival were similar between study arms.
CONCLUSIONS: Our data support micafungin as alternative antifungal prophylaxis in patients with AL and MDS.
Copyright © 2018 The British Infection Association. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Immunocompromised hosts; Invasive fungal infections; Leukemia; Micafungin; Myelodysplastic syndrome; Neutropenia; Posaconazole; Prophylaxis

Mesh:

Substances:

Year:  2018        PMID: 29746955      PMCID: PMC6800202          DOI: 10.1016/j.jinf.2018.03.015

Source DB:  PubMed          Journal:  J Infect        ISSN: 0163-4453            Impact factor:   6.072


  27 in total

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