Literature DB >> 19281327

Empirical versus preemptive antifungal therapy for high-risk, febrile, neutropenic patients: a randomized, controlled trial.

Catherine Cordonnier1, Cécile Pautas, Sébastien Maury, Anne Vekhoff, Hassan Farhat, Felipe Suarez, Nathalie Dhédin, Francoise Isnard, Lionel Ades, Frédérique Kuhnowski, Françoise Foulet, Mathieu Kuentz, Patrick Maison, Stéphane Bretagne, Michaël Schwarzinger.   

Abstract

BACKGROUND: Empirical antifungal therapy is the standard of care for neutropenic patients with hematological malignancies who remain febrile despite broad-spectrum antibacterial treatment. Recent diagnostic improvements may ensure the early diagnosis of potentially invasive fungal disease. Reserving antifungals for this stage may achieve similar survival rates and reduce treatment toxicity and costs.
METHODS: In this multicenter, open-label, randomized noninferiority trial, we compared an empirical antifungal strategy with a preemptive one. Empirical treatment was defined as antibacterial treatment of patients who have persistent or recurrent fever. Preemptive treatment was defined as treatment of patients who have clinical, imaging, or galactomannan-antigen-assay evidence suggesting fungal disease. First-line antifungal treatment was amphotericin B deoxycholate (1 mg/kg/day) or liposomal amphotericin (3 mg/kg/day), depending on daily renal function. The primary efficacy outcome was the proportion of patients alive at 14 days after recovery from neutropenia.
RESULTS: The median duration of neutropenia (neutrophil count, <500 cells/mm3) for the 293 patients enrolled was 18 days (range, 5-69 days). By intention-to-treat analysis, survival was 97.3% with empirical treatment and 95.1% with preemptive treatment. The lower 95% confidence limit for the difference in mortality was -5.9%, which was within the noninferiority margin of -8%. Probable or proven invasive fungal infections were more common among patients who received preemptive treatment than among patients who received empirical treatment (13 of 143 vs. 4 of 150; P < .05), and most infections occurred during induction therapy (12 of 73 patients in the preemptive treatment group vs. 3 of 78 patients in the empirical treatment group were infected during induction therapy; P < .01). Preemptive treatment did not decrease nephrotoxicity but decreased costs of antifungal therapy by 35%.
CONCLUSIONS: Preemptive treatment increased the incidence of invasive fungal disease, without increasing mortality, and decreased the costs of antifungal drugs. Empirical treatment may provide better survival rates for patients receiving induction chemotherapy.

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Year:  2009        PMID: 19281327     DOI: 10.1086/597395

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  94 in total

1.  Empirical versus pre-emptive antifungal therapy for persistent febrile neutropenia.

Authors:  Elio Castagnola; Riccardo Haupt
Journal:  Haematologica       Date:  2012-01       Impact factor: 9.941

2.  Canadian clinical practice guidelines for invasive candidiasis in adults.

Authors:  Eric J Bow; Gerald Evans; Jeff Fuller; Michel Laverdière; Coleman Rotstein; Robert Rennie; Stephen D Shafran; Don Sheppard; Sylvie Carle; Peter Phillips; Donald C Vinh
Journal:  Can J Infect Dis Med Microbiol       Date:  2010       Impact factor: 2.471

3.  Assessing responses to treatment of opportunistic mycoses and salvage strategies.

Authors:  Baldeep Wirk; John R Wingard
Journal:  Curr Infect Dis Rep       Date:  2011-12       Impact factor: 3.725

4.  Impact of invasive fungal disease on the chemotherapy schedule and event-free survival in acute leukemia patients who survived fungal disease: a case-control study.

Authors:  Caroline Even; Sylvie Bastuji-Garin; Yosr Hicheri; Cécile Pautas; Francoise Botterel; Sébastien Maury; Ludovic Cabanne; Stéphane Bretagne; Catherine Cordonnier
Journal:  Haematologica       Date:  2010-11-11       Impact factor: 9.941

5.  Cost-effectiveness analysis comparing two approaches for empirical antifungal therapy in hematological patients with persistent febrile neutropenia.

Authors:  Almudena Martín-Peña; M Victoria Gil-Navarro; Manuela Aguilar-Guisado; Ildefonso Espigado; Maite Ruiz Pérez de Pipaón; José Falantes; Jerónimo Pachón; José M Cisneros
Journal:  Antimicrob Agents Chemother       Date:  2013-07-15       Impact factor: 5.191

6.  The Role of Biomarkers for Diagnosis of and Therapeutic Decisions Related to Invasive Aspergillosis in Children.

Authors:  Brian T Fisher
Journal:  Curr Fungal Infect Rep       Date:  2013-03-01

7.  Economic evaluation of a preemptive treatment strategy for invasive fungal infection in neutropenic patients with hematological diseases.

Authors:  S-I Kimura; T Murata; Y Akahoshi; H Nakano; T Ugai; H Wada; R Yamasaki; Y Ishihara; K Kawamura; K Sakamoto; M Ashizawa; M Sato; K Terasako-Saito; H Nakasone; M Kikuchi; R Yamazaki; S Kako; J Kanda; A Tanihara; J Nishida; Y Kanda
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2015-01-11       Impact factor: 3.267

8.  Understanding the risk for infection in patients with neutropenia.

Authors:  Jean A Klastersky; Anne-Pascale Meert
Journal:  Intensive Care Med       Date:  2015-07-14       Impact factor: 17.440

9.  Serum galactomannan surveillance may be safely withdrawn from antifungal management of hematology patients on effective antimold prophylaxis: a pilot single-center study.

Authors:  R F Duarte; I Sánchez-Ortega; M Arnan; B Patiño; J Ayats; A Sureda; M Cuenca-Estrella
Journal:  Bone Marrow Transplant       Date:  2016-10-31       Impact factor: 5.483

10.  Invasive coinfection with Aspergillus and Mucor in a patient with acute myeloid leukemia.

Authors:  Rui Bergantim; Elisabete Rios; Fernanda Trigo; Jose Eduardo Guimarães
Journal:  Clin Drug Investig       Date:  2013-02       Impact factor: 2.859

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