Nature communications · 2026
A deep learning framework for efficient pathology image analysis.
СтатьяПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Neidlinger Peter, Lenz Tim, Foersch Sebastian, Loeffler Chiara M L, Clusmann Jan, Gustav Marco, Shaktah Lawrence A, Langer Rupert, Dislich Bastian, Boardman Lisa A, French Amy J, Goode Ellen L, Gsur Andrea, Brezina Stefanie, Gunter Marc J, Steinfelder Robert, Behrens Hans-Michael, Röcken Christoph, Harrison Tabitha, Peters Ulrike, Phipps Amanda I, Curigliano Giuseppe, Fusco Nicola, Marra Antonio, Hoffmeister Michael, Brenner Hermann, Kather Jakob Nikolas
Аннотация
Artificial intelligence has transformed digital pathology by enabling biomarker prediction from high-resolution whole-slide images. However, current methods are computationally inefficient, processing thousands of redundant tiles per slide and requiring complex aggregation models. We introduce EAGLE (Efficient Approach for Guided Local Examination), a deep learning framework that emulates pathologists by selectively analyzing informative regions. EAGLE combines task-agnostic tile selection with detailed feature extraction and is benchmarked against leading slide- and tile-level foundation models across 43 tasks from nine cancer types spanning morphology, biomarker prediction, treatment response and prognosis. EAGLE outperforms patch aggregation methods by up to 23% and achieves the highest overall classification performance. It processes one slide in 2.27 s, reducing computational time by more than 99% compared with existing models. This efficiency supports rapid and auditable workflows by enabling review of the exact tiles used for each prediction and reducing dependence on high-performance computing. By reliably identifying informative regions and minimizing artifacts, EAGLE provides robust and auditable outputs, supported by systematic negative controls and attention concentration analyses. Its unified embedding enables rapid slide search, integration into multi-omics pipelines and emerging clinical foundation models.