A multi-institutional review of outcomes in biopsy-proven chronic invasive fungal sinusitis.


Journal

International forum of allergy & rhinology
ISSN: 2042-6984
Titre abrégé: Int Forum Allergy Rhinol
Pays: United States
ID NLM: 101550261

Informations de publication

Date de publication:
06 2020
Historique:
received: 10 08 2019
revised: 16 01 2020
accepted: 21 01 2020
pubmed: 14 4 2020
medline: 12 8 2021
entrez: 14 4 2020
Statut: ppublish

Résumé

Chronic invasive fungal sinusitis (CIFS) is a rare, life-threatening infection of the nose and sinuses. This study aims to identify factors that impact survival in 1 of the largest cohorts to date. Pathology records were reviewed for biopsy-proven CIFS from 3 tertiary academic institutions from 1995 to 2016. Variables were analyzed using log-rank survival analysis. Univariate Cox regression was performed at 1 and 12 months. Thirty-eight patients were included. Hematologic malignancy and diabetes were the most common underlying diseases (32% each). Aspergillus was the most common fungus (63%). Greater than 75% of the patients had an absolute neutrophil count (ANC) >1000 at the time of diagnosis. Overall survival at 1, 6, and 12 months was 89%, 68%, and 48%, respectively. In univariate analysis, factors associated with worse survival included: ANC <500 at 12 months (hazard ratio [HR] 4.8; p = 0.01), ANC <1000 at 12 months (HR 5.8; p = 0.001), and recent chemotherapy (HR 4; p = 0.01). The following factor was associated with improved survival in univariate analysis: ANC as a linear variable in the entire cohort (HR 0.7; p = 0.005). We present a multi-institutional case-series of CIFS and long-term follow-up. ANC <1000 at time of diagnosis and recent chemotherapy (within 1 month of diagnosis) are associated with poorer survival, whereas a rising ANC >1000 is associated with improved survival at 12 months. Further prospective studies are needed to further define factors that affect outcomes.

Sections du résumé

BACKGROUND
Chronic invasive fungal sinusitis (CIFS) is a rare, life-threatening infection of the nose and sinuses. This study aims to identify factors that impact survival in 1 of the largest cohorts to date.
METHODS
Pathology records were reviewed for biopsy-proven CIFS from 3 tertiary academic institutions from 1995 to 2016. Variables were analyzed using log-rank survival analysis. Univariate Cox regression was performed at 1 and 12 months.
RESULTS
Thirty-eight patients were included. Hematologic malignancy and diabetes were the most common underlying diseases (32% each). Aspergillus was the most common fungus (63%). Greater than 75% of the patients had an absolute neutrophil count (ANC) >1000 at the time of diagnosis. Overall survival at 1, 6, and 12 months was 89%, 68%, and 48%, respectively. In univariate analysis, factors associated with worse survival included: ANC <500 at 12 months (hazard ratio [HR] 4.8; p = 0.01), ANC <1000 at 12 months (HR 5.8; p = 0.001), and recent chemotherapy (HR 4; p = 0.01). The following factor was associated with improved survival in univariate analysis: ANC as a linear variable in the entire cohort (HR 0.7; p = 0.005).
CONCLUSION
We present a multi-institutional case-series of CIFS and long-term follow-up. ANC <1000 at time of diagnosis and recent chemotherapy (within 1 month of diagnosis) are associated with poorer survival, whereas a rising ANC >1000 is associated with improved survival at 12 months. Further prospective studies are needed to further define factors that affect outcomes.

Identifiants

pubmed: 32282122
doi: 10.1002/alr.22547
doi:

Substances chimiques

Antifungal Agents 0

Types de publication

Case Reports Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

738-747

Informations de copyright

© 2020 ARS-AAOA, LLC.

Références

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Auteurs

Ian M Humphreys (IM)

Department of Otolaryngology, University of Washington, Seattle, WA.

Grace M Wandell (GM)

Department of Otolaryngology, University of Washington, Seattle, WA.

Craig Miller (C)

Department of Otolaryngology, University of Washington, Seattle, WA.

Aakanksha Rathor (A)

Department of Otolaryngology, Stanford University, Stanford, CA.

Rodney A Schmidt (RA)

Department of Pathology, University of Washington, Seattle, WA.

Justin H Turner (JH)

Department of Otolaryngology, Vanderbilt University, Nashville, TN.

Peter H Hwang (PH)

Department of Otolaryngology, Stanford University, Stanford, CA.

Greg E Davis (GE)

Department of Otolaryngology, University of Washington, Seattle, WA.

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