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dc.contributor.author
Pati, Pushpak
dc.contributor.author
Karkampouna, Sofia
dc.contributor.author
Bonollo, Francesco
dc.contributor.author
Compérat, Eva
dc.contributor.author
Radić, Martina
dc.contributor.author
Spahn, Martin
dc.contributor.author
Martinelli, Adriano
dc.contributor.author
Wartenberg, Martin
dc.contributor.author
Kruithof‑de Julio, Marianna
dc.contributor.author
Rapsomaniki, Marianna
dc.date.accessioned
2024-09-30T15:29:46Z
dc.date.available
2024-09-17T05:00:58Z
dc.date.available
2024-09-17T14:10:58Z
dc.date.available
2024-09-30T15:29:46Z
dc.date.issued
2024-09
dc.identifier.issn
2522-5839
dc.identifier.other
10.1038/s42256-024-00889-5
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/694315
dc.identifier.doi
10.3929/ethz-b-000694315
dc.description.abstract
Understanding the spatial heterogeneity of tumours and its links to disease initiation and progression is a cornerstone of cancer biology. Presently, histopathology workflows heavily rely on hematoxylin and eosin and serial immunohistochemistry staining, a cumbersome, tissue-exhaustive process that results in non-aligned tissue images. We propose the VirtualMultiplexer, a generative artificial intelligence toolkit that effectively synthesizes multiplexed immunohistochemistry images for several antibody markers (namely AR, NKX3.1, CD44, CD146, p53 and ERG) from only an input hematoxylin and eosin image. The VirtualMultiplexer captures biologically relevant staining patterns across tissue scales without requiring consecutive tissue sections, image registration or extensive expert annotations. Thorough qualitative and quantitative assessment indicates that the VirtualMultiplexer achieves rapid, robust and precise generation of virtually multiplexed imaging datasets of high staining quality that are indistinguishable from the real ones. The VirtualMultiplexer is successfully transferred across tissue scales and patient cohorts with no need for model fine-tuning. Crucially, the virtually multiplexed images enabled training a graph transformer that simultaneously learns from the joint spatial distribution of several proteins to predict clinically relevant endpoints. We observe that this multiplexed learning scheme was able to greatly improve clinical prediction, as corroborated across several downstream tasks, independent patient cohorts and cancer types. Our results showcase the clinical relevance of artificial intelligence-assisted multiplexed tumour imaging, accelerating histopathology workflows and cancer biology.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Nature
en_US
dc.rights.uri
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
Cancer imaging
en_US
dc.subject
Machine learning
en_US
dc.title
Accelerating histopathology workflows with generative AI-based virtually multiplexed tumour profiling
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
dc.date.published
2024-09-09
ethz.journal.title
Nature Machine Intelligence
ethz.journal.volume
6
en_US
ethz.journal.issue
9
en_US
ethz.journal.abbreviated
Nat Mach Intell
ethz.pages.start
1077
en_US
ethz.pages.end
1093
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.status
published
en_US
ethz.date.deposited
2024-09-17T05:01:16Z
ethz.source
WOS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2024-09-30T15:29:47Z
ethz.rosetta.lastUpdated
2024-09-30T15:29:47Z
ethz.rosetta.versionExported
true
ethz.COinS
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