Usefulness of serum galactomannan in initiating and modifying antifungal therapy in children with cancer and persistent high-risk febrile neutropenia.


Journal

Mycoses
ISSN: 1439-0507
Titre abrégé: Mycoses
Pays: Germany
ID NLM: 8805008

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 31 01 2020
revised: 20 04 2020
accepted: 21 04 2020
pubmed: 30 4 2020
medline: 10 4 2021
entrez: 30 4 2020
Statut: ppublish

Résumé

Invasive fungal disease is a major cause of morbidity and mortality in children with cancer and high-risk febrile neutropenia (HRFN). Repeated serum galactomannan (sGM) measurements have been described as an effective tool to guide therapy in adults under suspicion of invasive aspergillosis. However, the utility of this approach has not been reported in paediatric population. To evaluate the usefulness of sGM measurements in initiating and modifying antifungal therapy (AFT) in children with cancer and persistent HRFN. Nested case-control study in children with cancer and persistent HRFN episodes, between July 2013 and January 2019. Patients were classified as cases and controls depending on if they received AFT or not, respectively. Through odds ratio analysis, we assessed the role of sGM positivity in the AFT initiation decision. Then, we analysed the group of patients that initiated AFT, and compared those who had AFT modifications and those who did not, analysing different sGM kinetics thresholds. A total of 191 episodes from children with persistent HRFN were enrolled, of which 107 received AFT and 84 did not. The median age was 7 years (IQR 4-12), 52% were male and 89% had a haematologic malignancy as underlying disease. Positive sGM was not associated with AFT initiation (OR 0.99, 95% CI 0.43-2.33, P = .99). A difference threshold in sGM Δ ≥ 0.3 sGM was significantly associated with AFT modification (OR 5.07, 95% CI 1.02- 25.70, P = .04). Our results suggest the utility of serial sGM sampling during AFT in children with persistent HRFN.

Sections du résumé

BACKGROUND BACKGROUND
Invasive fungal disease is a major cause of morbidity and mortality in children with cancer and high-risk febrile neutropenia (HRFN). Repeated serum galactomannan (sGM) measurements have been described as an effective tool to guide therapy in adults under suspicion of invasive aspergillosis. However, the utility of this approach has not been reported in paediatric population.
OBJECTIVES OBJECTIVE
To evaluate the usefulness of sGM measurements in initiating and modifying antifungal therapy (AFT) in children with cancer and persistent HRFN.
PATIENTS/METHODS METHODS
Nested case-control study in children with cancer and persistent HRFN episodes, between July 2013 and January 2019. Patients were classified as cases and controls depending on if they received AFT or not, respectively. Through odds ratio analysis, we assessed the role of sGM positivity in the AFT initiation decision. Then, we analysed the group of patients that initiated AFT, and compared those who had AFT modifications and those who did not, analysing different sGM kinetics thresholds.
RESULTS RESULTS
A total of 191 episodes from children with persistent HRFN were enrolled, of which 107 received AFT and 84 did not. The median age was 7 years (IQR 4-12), 52% were male and 89% had a haematologic malignancy as underlying disease. Positive sGM was not associated with AFT initiation (OR 0.99, 95% CI 0.43-2.33, P = .99). A difference threshold in sGM Δ ≥ 0.3 sGM was significantly associated with AFT modification (OR 5.07, 95% CI 1.02- 25.70, P = .04).
CONCLUSIONS CONCLUSIONS
Our results suggest the utility of serial sGM sampling during AFT in children with persistent HRFN.

Identifiants

pubmed: 32347600
doi: 10.1111/myc.13097
doi:

Substances chimiques

Antifungal Agents 0
Mannans 0
galactomannan 11078-30-1
Galactose X2RN3Q8DNE

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

802-811

Subventions

Organisme : Fondo Nacional de Desarrollo Científico y Tecnológico
ID : 1120800
Organisme : Fondo Nacional de Desarrollo Científico y Tecnológico
ID : 1161662

Informations de copyright

© 2020 Blackwell Verlag GmbH.

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Auteurs

Matías Delgado-Araneda (M)

Department of Pediatrics, Residency and Medical Sciences Doctorate Program, Faculty of Medicine, Universidad de Chile, Santiago, Chile.

Romina Valenzuela (R)

Department of Pediatrics, Faculty of Medicine, Hospital Dr. Luis Calvo Mackenna, Universidad de Chile, Santiago, Chile.

Verónica de la Maza (V)

Department of Pediatrics, Faculty of Medicine, Hospital Dr. Luis Calvo Mackenna, Universidad de Chile, Santiago, Chile.

Marcela Rabello (M)

Department of Pediatrics, Faculty of Medicine, Hospital Dr. Luis Calvo Mackenna, Universidad de Chile, Santiago, Chile.

Ana M Álvarez (AM)

Department of Pediatrics, Faculty of Medicine, Hospital San Juan de Dios, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Verónica Contardo (V)

Department of Pediatrics, Faculty of Medicine, Hospital Roberto del Río, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Marcela Zubieta (M)

Department of Pediatrics, Hospital Exequiel González Cortés, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Valentina Gutierrez (V)

Department of Pediatrics, Hospital Dr. Sótero del Río, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Ximena Claverie (X)

Department of Pediatrics, Hospital Dr. Sótero del Río, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Juan P Torres (JP)

Department of Pediatrics, Faculty of Medicine, Hospital Dr. Luis Calvo Mackenna, Universidad de Chile, Santiago, Chile.

Carmen Salgado (C)

Department of Pediatrics, Hospital Exequiel González Cortés, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Juan Tordecilla (J)

Department of Pediatrics, Faculty of Medicine, Hospital Roberto del Río, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Mónica Varas (M)

Department of Pediatrics, Faculty of Medicine, Hospital San Juan de Dios, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Carmen L Avilés (CL)

Department of Pediatrics, Faculty of Medicine, Hospital San Borja Arriarán, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Marcela Venegas (M)

Department of Pediatrics, Faculty of Medicine, Hospital San Borja Arriarán, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

Milena Villarroel (M)

Department of Pediatrics, Faculty of Medicine, Hospital Dr. Luis Calvo Mackenna, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

María E Santolaya (ME)

Department of Pediatrics, Faculty of Medicine, Hospital Dr. Luis Calvo Mackenna, Universidad de Chile, Santiago, Chile.
Committee of Infectious Diseases, National Child Programme of Antineoplastic Drugs (PINDA), Santiago, Chile.

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