A team of scientists around Dr. Tingying Peng from Helmholtz Munich and Prof. Jakob N. Kather from TU Dresden show that AI can predict specific biomarkers in stained tissue samples of patients with CRC. They used so-called transformer networks, a recent deep learning (DL) approach, to identify patterns and support diagnostic decisions in cancer management. The new method significantly improves previous approaches for biomarker detection.
Large-Scale Evaluation Proves Better Generalization and Data-EfficiencyThe team of researchers developed software that uses the new technology of transformer neural networks throughout the analysis process. They show that their approach substantially improves the performance, generalizability, data efficiency, and interpretability by evaluating it on a large multicentric cohort of over 13,000 patients from 16 cohorts from seven countries (Australia, China, Germany, Israel, Netherlands, UK, USA), part of which was contributed by researchers at the German Cancer Research Center (DKFZ) Heidelberg and the network of the National Centers for Tumor Diseases (NCT). The algorithm trained on the large multicentric cohort achieves a very high sensitivity on resection tissue samples obtained during surgery. Strikingly, even though their model has only been trained on tissue samples from resections, the results can reach also a high performance on biopsy tissue obtained during colonoscopy. Sophia J. Wagner, the first author of the study, emphasizes that “the generalization to biopsy tissue increases the algorithm’s benefit for the patient when ultimately implemented in clinical routine”.
AI-Based Pre-screening for Biopsies Accelerate DiagnosisBecause of its high sensitivity on biopsy tissue, the algorithm could serve as a pre-screening tool followed by affirmative testing for cases that received a positive result during AI testing. Applying AI-based biomarker prediction could reduce the testing burden and therefore speed up the step between taking the biopsy and the molecular determination of the genetic risk status, thus enabling an earlier patient treatment with immunotherapy if indicated.
Sophia J Wagner, Daniel Reisenbüchler, Nicholas P West, Jan Moritz Niehues, Jiefu Zhu, Sebastian Foersch, Gregory Patrick Veldhuizen, Philip Quirke, Heike I Grabsch, Piet A van den Brandt, Gordon GA Hutchins, Susan D Richman, Tanwei Yuan, Rupert Langer, Josien CA Jenniskens, Kelly Offermans, Wolfram Mueller, Richard Gray, Stephen B Gruber, Joel K Greenson, Gad Rennert, Joseph D Bonner, Daniel Schmolze, Jitendra Jonnagaddala, Nicholas J Hawkins, Robyn L Ward, Dion Morton, Matthew Seymour, Laura Magill, Marta Nowak, Jennifer Hay, Viktor H Koelzer, David N Church, David Church, Enric Domingo, Joanne Edwards, Bengt Glimelius, Ismail Gogenur, Andrea Harkin, Jen Hay, Timothy Iveson, Emma Jaeger, Caroline Kelly, Rachel Kerr, Noori Maka, Hannah Morgan, Karin Oien, Clare Orange, Claire Palles, Campbell Roxburgh, Owen Sansom, Mark Saunders, Ian Tomlinson, Christian Matek, Carol Geppert, Chaolong Peng, Cheng Zhi, Xiaoming Ouyang, Jacqueline A James, Maurice B Loughrey, Manuel Salto-Tellez, Hermann Brenner, Michael Hoffmeister, Daniel Truhn, Julia A Schnabel, Melanie Boxberg, Tingying Peng, Jakob Nikolas Kather.
Transformer-based biomarker prediction from colorectal cancer histology: A large-scale multicentric study.
Cancer Cell, 2023. doi: 10.1016/j.ccell.2023.08.002