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 : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
18 02 2023
Historique:
received: 01 03 2022
pubmed: 31 7 2022
medline: 25 2 2023
entrez: 30 7 2022
Statut: ppublish

Résumé

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.

Sections du résumé

BACKGROUND
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.
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.

Identifiants

pubmed: 35906831
pii: 6652161
doi: 10.1093/cid/ciac623
pmc: PMC9938744
doi:

Substances chimiques

Antifungal Agents 0
Fluconazole 8VZV102JFY
Caspofungin F0XDI6ZL63

Banques de données

ClinicalTrials.gov
['NCT01288378']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

674-682

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. J. M. reports consulting fees and payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from MSD, Gilead Sciences, and Pfizer, including participation on a data and safety monitoring board or advisory board (DSMB) for MSD, Gilead, and Pfizer. T. L. reports payment for participation on virtual European Society for Blood and Marrow Transplantation meeting. J. P. D. reports consulting fees from F2G and Gilead Sciences, including payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from F2G, Gilead Sciences, and Pfizer, and unpaid leadership or fiduciary role in other board, society, committee, or advocacy group for the European PCR Initiative Foundation. C. R. reports payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Gilead and Sandoz and support for attending meetings and/or travel for Gilead, MSD, Pfizer, and Sandoz. N. B. reports participation as the chair on a DSMB for the SHORT trial and roles as the president of the Dutch Society of Hematology (unpaid), Treasurer Board member for HOVON (unpaid), chair of the Horizonscan WP Hematology Dutch Healthcare Institute (vacancy fee), and member of the board of supervisors for Matchis (compensation according to Dutch law). D. S. reports grants or contracts from Pfizer, Novartis, BMS, AbbVie, MSD, and Takeda, including consulting fees from Pfizer, Novartis, AbbVie, BMS, Takeda, MSD, Janssen-Cilag, and Astellas; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Pfizer, Novartis, AbbVie, BMS, Takeda, MSD, and Janssen-Cilag; support for attending meetings and/or travel from Pfizer, Novartis, BMS, AbbVie, Takeda, MSD, and Janssen-Cilag; and a leadership or fiduciary role for other board, society, committee, or advocacy groups, paid or unpaid for Belgian College for Reimbursement of Orphan Drugs. F. B. reports payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from AbbVie and Sanofi; support for attending an international meeting from Novartis and Pfizer; and participation on a DSMB or advisory board for some academic studies (no fee) and Maatpharma (paid to institution). W. J. H. reports payment or honoraria for presentations from AbbVie, Amgen, AstraZeneca, Celgene/BMS, Gilead Sciences, and Janssen; support for attending meetings from IPSEN Pharma, Amgen, and Abbvie; and support for attending adboards for Amgen, Astrazeneca, Celgene/BMS, Gilead Sciences Janssen, MSD, and Sanofi-Aventis. B. V. reports payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Pfizer, Sanofi, and Al Miral; support for attending meetings and/or travel for ViiV; and participation on a DSMB or advisory board for Pfizer. L. D. reports consulting fees from MSD, Pfizer, and Teva; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from MSD, Pfizer, Teva, and Sandoz; support for attending meetings and/or travel from Sandoz; and participation on an advisory board for Pfizer. C. C. L. reports payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Gilead and Kite and support for attending meetings and/or travel for Gilead and Kite. C. S. P. reports book royalties from Elsevier and Thieme and honoraria for lectures from Canon Medical Systems. R. B. reports consulting fees from Gilead; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Gilead; and support for attending meetings and/or travel for Gilead. P. E. V. reports research grants from ZonMw, Welcome Trust, Eurostars, EORTC, and RIVM; consulting fees from F2G, Gilead Sciences, and Pfizer; and payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Gilead Sciences and Pfizer. F. L. reports research grants from Merck, Sharpe & Dohme, Gilead, Pfizer, and Novartis and consulting fees (advisory board) from Gilead and Pfizer. P. Y. B. reports payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Gilead Sciences Switzerland AG and Pfizer PFE Switzerland GmbH and support for Gilead Sciences Switzerland Sarl for TIMM, Trends in Medical Mycology. D. H. reports employment with Merck & Co. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Johan Maertens (J)

Department of Hematology, University Hospitals Leuven, Leuven, Belgium.

Tom Lodewyck (T)

Department of Hematology, Algemeen Ziekenhuis St Jan, Brugge, Belgium.

J Peter Donnelly (JP)

Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.

Sylvain Chantepie (S)

Department of Hematology, Caen University Hospital, Caen, France.

Christine Robin (C)

Department of Hematology, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.

Nicole Blijlevens (N)

Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.

Pascal Turlure (P)

Department of Hematology, Centre Hospitalier Universitaire Limoges, Limoges, France.

Dominik Selleslag (D)

Department of Hematology, Algemeen Ziekenhuis St Jan, Brugge, Belgium.

Frédéric Baron (F)

Department of Hematology, University of Liège and University Hospital of Liège, Liège, Belgium.

Mickael Aoun (M)

Department of Internal Medicine, Institut Jules Bordet, Brussels, Belgium.

Werner J Heinz (WJ)

Department of Hematology/Oncology, Caritas Hospital, Bad Mergentheim, Germany.

Hartmut Bertz (H)

Department of Hematology/Oncology, Faculty of Medicine and Medical Centre, University of Freiburg, Freiburg, Germany.

Zdeněk Ráčil (Z)

Department of Hematology, Masaryk University Brno and Institute of Hematology and Blood Transfusion, Prague, Czech Republic.

Bernard Vandercam (B)

Department of Internal Medicine/Infectious Diseases, Cliniques Universitaires St. Luc, Brussels, Belgium.

Lubos Drgona (L)

Department of Oncohematology, Comenius University and National Cancer Institute, Bratislava, Slovakia.

Valerie Coiteux (V)

Service des maladies du sang, Centre Hospitalier Régional Universitaire Lille, Lille, France.

Cristina Castilla Llorente (CC)

Department of Hematology, Gustave Roussy Cancer Campus, Villejuif, France.

Cornelia Schaefer-Prokop (C)

Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.

Marianne Paesmans (M)

Department of Internal Medicine, Institut Jules Bordet, Brussels, Belgium.

Lieveke Ameye (L)

Department of Internal Medicine, Institut Jules Bordet, Brussels, Belgium.

Liv Meert (L)

European Organisation for Research and Treatment of Cancer Headquarters, Brussels, Belgium.

Kin Jip Cheung (KJ)

European Organisation for Research and Treatment of Cancer Headquarters, Brussels, Belgium.

Deborah A Hepler (DA)

Merck & Co, Inc, Kenilworth, New Jersey, USA.

Jürgen Loeffler (J)

Department of Internal Medicine II, Universitaetsklinikum, Würzburg, Germany.

Rosemary Barnes (R)

Department of Infection, Immunity and Biochemistry, Cardiff University, Cardiff, United Kingdom.

Oscar Marchetti (O)

Department of Medicine, Lausanne University Hospital, Lausanne, Switzerland.
Department of Infectious Diseases, Ensemble Hospitalier de la Côte, Morges, Switzerland.

Paul Verweij (P)

Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.

Frederic Lamoth (F)

Department of Medicine, Lausanne University Hospital, Lausanne, Switzerland.

Pierre-Yves Bochud (PY)

Department of Medicine, Lausanne University Hospital, Lausanne, Switzerland.

Michael Schwarzinger (M)

Translational Health Economics Network, Bordeaux University Hospital, Bordeaux, France.

Catherine Cordonnier (C)

Department of Hematology, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.

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