Machine learning-based prediction of glioma margin from 5-ALA induced PpIX fluorescence spectroscopy.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
29 01 2020
Historique:
received: 05 07 2019
accepted: 06 01 2020
entrez: 31 1 2020
pubmed: 31 1 2020
medline: 14 7 2020
Statut: epublish

Résumé

Gliomas are infiltrative brain tumors with a margin difficult to identify. 5-ALA induced PpIX fluorescence measurements are a clinical standard, but expert-based classification models still lack sensitivity and specificity. Here a fully automatic clustering method is proposed to discriminate glioma margin. This is obtained from spectroscopic fluorescent measurements acquired with a recently introduced intraoperative set up. We describe a data-driven selection of best spectral features and show how this improves results of margin prediction from healthy tissue by comparison with the standard biomarker-based prediction. This pilot study based on 10 patients and 50 samples shows promising results with a best performance of 77% of accuracy in healthy tissue prediction from margin tissue.

Identifiants

pubmed: 31996727
doi: 10.1038/s41598-020-58299-7
pii: 10.1038/s41598-020-58299-7
pmc: PMC6989497
doi:

Substances chimiques

Biomarkers, Tumor 0
Protoporphyrins 0
Aminolevulinic Acid 88755TAZ87
protoporphyrin IX C2K325S808

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1462

Références

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Auteurs

Pierre Leclerc (P)

Univ Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, F-69622, Villeurbanne, France, 10 Rue Ada Byron, 69622, Villeurbanne, France.
CREATIS, Univ Lyon, CNRS UMR5220, INSERM U1044, Université Claude Bernard Lyon1, INSA Lyon, Villeurbanne, France.

Cedric Ray (C)

Univ Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, F-69622, Villeurbanne, France, 10 Rue Ada Byron, 69622, Villeurbanne, France.

Laurent Mahieu-Williame (L)

CREATIS, Univ Lyon, CNRS UMR5220, INSERM U1044, Université Claude Bernard Lyon1, INSA Lyon, Villeurbanne, France.

Laure Alston (L)

CREATIS, Univ Lyon, CNRS UMR5220, INSERM U1044, Université Claude Bernard Lyon1, INSA Lyon, Villeurbanne, France.

Carole Frindel (C)

CREATIS, Univ Lyon, CNRS UMR5220, INSERM U1044, Université Claude Bernard Lyon1, INSA Lyon, Villeurbanne, France.

Pierre-François Brevet (PF)

Univ Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, F-69622, Villeurbanne, France, 10 Rue Ada Byron, 69622, Villeurbanne, France.

David Meyronet (D)

Hospices Civils de Lyon, Centre de Pathologie et de Neuropathologie Est, Lyon, F-69003, France.
Cancer Research Centre of Lyon, Univ Lyon, INSERM U1052, CNRS UMR5286, Lyon, France, Université Claude Bernard Lyon 1, Lyon, France.

Jacques Guyotat (J)

Hospices Civils de Lyon, Centre de Pathologie et de Neuropathologie Est, Lyon, F-69003, France.

Bruno Montcel (B)

CREATIS, Univ Lyon, CNRS UMR5220, INSERM U1044, Université Claude Bernard Lyon1, INSA Lyon, Villeurbanne, France. bruno.montcel@univ-lyon1.fr.

David Rousseau (D)

CREATIS, Univ Lyon, CNRS UMR5220, INSERM U1044, Université Claude Bernard Lyon1, INSA Lyon, Villeurbanne, France.
Laboratoire Angevin de Recherche en Ingénierie des Systèmes, UMR INRA IRHS, Université d'Angers, 62 avenue Notre Dame du Lac, 49000, Angers, France.

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