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dc.contributor.authorHewitt, KJ
dc.contributor.authorLöffler, CML
dc.contributor.authorMuti, HS
dc.contributor.authorBerghoff, AS
dc.contributor.authorEisenlöffel, C
dc.contributor.authorvan Treeck, M
dc.contributor.authorCarrero, ZI
dc.contributor.authorEl Nahhas, OSM
dc.contributor.authorVeldhuizen, GP
dc.contributor.authorWeil, S
dc.contributor.authorSaldanha, OL
dc.contributor.authorBejan, L
dc.contributor.authorMillner, TO
dc.contributor.authorBrandner, S
dc.contributor.authorBrückmann, S
dc.contributor.authorKather, JN
dc.date.accessioned2024-01-02T15:05:13Z
dc.date.available2024-01-02T15:05:13Z
dc.date.issued2023-11-01
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/93257
dc.description.abstractBACKGROUND: Deep Learning (DL) can predict molecular alterations of solid tumors directly from routine histopathology slides. Since the 2021 update of the World Health Organization (WHO) diagnostic criteria, the classification of brain tumors integrates both histopathological and molecular information. We hypothesize that DL can predict molecular alterations as well as WHO subtyping of brain tumors from hematoxylin and eosin-stained histopathology slides. METHODS: We used weakly supervised DL and applied it to three large cohorts of brain tumor samples, comprising N = 2845 patients. RESULTS: We found that the key molecular alterations for subtyping, IDH and ATRX, as well as 1p19q codeletion, were predictable from histology with an area under the receiver operating characteristic curve (AUROC) of 0.95, 0.90, and 0.80 in the training cohort, respectively. These findings were upheld in external validation cohorts with AUROCs of 0.90, 0.79, and 0.87 for prediction of IDH, ATRX, and 1p19q codeletion, respectively. CONCLUSIONS: In the future, such DL-based implementations could ease diagnostic workflows, particularly for situations in which advanced molecular testing is not readily available.en_US
dc.format.extentvdad139 - ?
dc.languageeng
dc.publisherOxford University Pressen_US
dc.relation.ispartofNeurooncol Adv
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectIDHen_US
dc.subjectadult-type diffuse gliomasen_US
dc.subjectdeep learningen_US
dc.subjectmolecular signaturesen_US
dc.subjectsubtypeen_US
dc.titleDirect image to subtype prediction for brain tumors using deep learningen_US
dc.typeArticleen_US
dc.identifier.doi10.1093/noajnl/vdad139
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38106649en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume5en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States