Validation of a multivariable prediction model for post-engraftment invasive fungal disease in 465 adult allogeneic hematopoietic stem cell transplant recipients.


Journal

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

Informations de publication

Date de publication:
May 2019
Historique:
received: 05 07 2018
revised: 28 12 2018
accepted: 04 01 2019
pubmed: 12 1 2019
medline: 21 5 2019
entrez: 12 1 2019
Statut: ppublish

Résumé

Recently, we reported a simple prognostic score for post-engraftment invasive fungal disease (IFD) obtained in 404 adult allogeneic hematopoietic stem cell transplant (alloSCT) (training cohort). We aim to validate this score in an external cohort assessing the 1-year cumulative incidence (CI) of post-engraftment IFD. Additionally, we analyse the type of IFD and incidence of IFD according to type of prophylaxis. We included 465 consecutive adult recipients surviving >40 days who engrafted and were discharged without prior IFD (median age 45 years, range, 14-69). Patients classified as low-risk, 139; intermediate-risk, 162; and high-risk, 164 (35% vs 27% in the training cohort, P = 0.03). The CI of probable/proven IFD in the validation cohort was 8% vs 11% in the training cohort (P = 0.006). The only voriconazole prophylaxis used in the training cohort was 100 mg/12 h, 65% vs 27% in the validation cohort, but 38% received 200 mg/12 h. Thus, the validation cohort showed a lower CI of IFD (P = 0.009). The post-engraftment IFD score was validated, showing a CI of IFD for low-, intermediate- and high-risk of 3%, 6% and 14%, respectively (P < 0.001). To our knowledge, this is the first prognostic index to predict the occurrence of post-engraftment IFD after alloSCT that has been validated in an external cohort.

Sections du résumé

BACKGROUND BACKGROUND
Recently, we reported a simple prognostic score for post-engraftment invasive fungal disease (IFD) obtained in 404 adult allogeneic hematopoietic stem cell transplant (alloSCT) (training cohort).
OBJECTIVES OBJECTIVE
We aim to validate this score in an external cohort assessing the 1-year cumulative incidence (CI) of post-engraftment IFD. Additionally, we analyse the type of IFD and incidence of IFD according to type of prophylaxis.
PATIENTS/METHODS METHODS
We included 465 consecutive adult recipients surviving >40 days who engrafted and were discharged without prior IFD (median age 45 years, range, 14-69).
RESULTS RESULTS
Patients classified as low-risk, 139; intermediate-risk, 162; and high-risk, 164 (35% vs 27% in the training cohort, P = 0.03). The CI of probable/proven IFD in the validation cohort was 8% vs 11% in the training cohort (P = 0.006). The only voriconazole prophylaxis used in the training cohort was 100 mg/12 h, 65% vs 27% in the validation cohort, but 38% received 200 mg/12 h. Thus, the validation cohort showed a lower CI of IFD (P = 0.009). The post-engraftment IFD score was validated, showing a CI of IFD for low-, intermediate- and high-risk of 3%, 6% and 14%, respectively (P < 0.001).
CONCLUSION CONCLUSIONS
To our knowledge, this is the first prognostic index to predict the occurrence of post-engraftment IFD after alloSCT that has been validated in an external cohort.

Identifiants

pubmed: 30633829
doi: 10.1111/myc.12891
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

418-427

Subventions

Organisme : Asociación Medicina e Investigación (A.M.I.)
Organisme : Instituto de Investigación Sanitaria La Fe
ID : 2012/023

Informations de copyright

© 2019 Blackwell Verlag GmbH.

Auteurs

Rebeca Rodríguez-Veiga (R)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.

Pau Montesinos (P)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
CIBERONC, Instituto Carlos III, Madrid, Spain.

Estefanía García (E)

Department of Hematology, Hospital Universitario Reina Sofía, Córdoba, Spain.

Blanca Boluda (B)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.

Rafael Rojas (R)

Department of Hematology, Hospital Universitario Reina Sofía, Córdoba, Spain.

Josefina Serrano (J)

Department of Hematology, Hospital Universitario Reina Sofía, Córdoba, Spain.

David Martínez-Cuadrón (D)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
CIBERONC, Instituto Carlos III, Madrid, Spain.

Carmen Martín (C)

Department of Hematology, Hospital Universitario Reina Sofía, Córdoba, Spain.

Jaime Sanz (J)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
CIBERONC, Instituto Carlos III, Madrid, Spain.

Salvador Tabares (S)

Department of Hematology, Hospital Universitario Reina Sofía, Córdoba, Spain.

José L Piñana (JL)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.

Ignacio Lorenzo (I)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.

Juan Montoro (J)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.

Miguel Salavert (M)

Department of Infectious Diseases, Hospital Universitari i Politècnic La Fe, València, Spain.

Javier Pemán (J)

Department of Microbiology, Hospital Universitari i Politècnic La Fe, València, Spain.

Isidro Jarque (I)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
CIBERONC, Instituto Carlos III, Madrid, Spain.

Pilar Solves (P)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
CIBERONC, Instituto Carlos III, Madrid, Spain.

Guillermo F Sanz (GF)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
CIBERONC, Instituto Carlos III, Madrid, Spain.

Antonio Torres (A)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
Asociación Medicina e Investigación (A.M.I.), Córdoba, Spain.

Miguel A Sanz (MA)

Department of Hematology, Hospital Universitari i Politècnic La Fe, València, Spain.
CIBERONC, Instituto Carlos III, Madrid, Spain.

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