The case for homebrew AI in diagnostic pathology

Artificial intelligence (AI) methods for digital pathology have tremendous potential to improve cancer diagnostics, biomarkers, and ultimately patient care. These AI methods, if marketed and sold, require authorisation or clearance as in vitro diagnostic (IVD) devices by regulatory bodies like the F...

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Bibliographic Details
Main Authors: Caldéraro, Julien (Author) , Morement, Helen (Author) , Penault-Llorca, Frédérique (Author) , Gilbert, Stephen (Author) , Kather, Jakob Nikolas (Author)
Format: Article (Journal)
Language:English
Published: August 2025
In: The journal of pathology
Year: 2025, Volume: 266, Issue: 4-5, Pages: 390-394
ISSN:1096-9896
DOI:10.1002/path.6438
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/path.6438
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/path.6438
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Author Notes:Julien Calderaro, Helen Morement, Frédérique Penault-Llorca, Stephen Gilbert and Jakob Nikolas Kather
Description
Summary:Artificial intelligence (AI) methods for digital pathology have tremendous potential to improve cancer diagnostics, biomarkers, and ultimately patient care. These AI methods, if marketed and sold, require authorisation or clearance as in vitro diagnostic (IVD) devices by regulatory bodies like the Food and Drug Administration (FDA) in the USA or Notified Bodies in the European Union (EU). Many AI tools for digital pathology are unlikely to be commercially viable and taken up by commercial entities ready to navigate these complex and costly processes. However, a longstanding quality framework already exists that allows for lab-developed tests, colloquially known as ‘homebrew’ tests, that are locally validated and performed under the responsibility and oversight of the pathologist. Here we argue for advancing homebrew AI systems within this existing framework to enhance patients' access to supportive digital diagnostic tools. We outline how homebrew AI models are currently permitted under regulatory provisions in the USA and the European Union, how a new US FDA rule may effectively regulate them out of existence, and propose steps to facilitate the safe and effective integration of homebrew AI models in pathology practice. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
Item Description:Zuerst veröffentlicht: 04. Juli 2025
Gesehen am 06.11.2025
Physical Description:Online Resource
ISSN:1096-9896
DOI:10.1002/path.6438