AI-powered spatial cell phenomics enhances risk stratification in non-small cell lung cancer
Authors
- Simon Schallenberg
- Gabriel Dernbach
- Sharon Ruane
- Philipp Jurmeister
- Cornelius Böhm
- Kai Standvoss
- Sandip Ghosh
- Marco Frentsch
- Mihnea P Dragomir
- Philipp G Keyl
- Corinna Friedrich
- Il-Kang Na
- Sabine Merkelbach-Bruse
- Alexander Quaas
- Nikolaj Frost
- Kyrill Boschung
- Winfried Randerath
- Georg Schlachtenberger
- Matthias Heldwein
- Ulrich Keilholz
- Khosro Hekmat
- Jens-Carsten Rückert
- Reinhard Büttner
- Angela Vasaturo
- David Horst
- Lukas Ruff
- Maximilian Alber
- Klaus-Robert Müller
- Frederick Klauschen
Journal
- Nature Communications
Citation
- Nat Commun 16 (1): 9701
Abstract
Risk stratification remains a critical challenge in non-small cell lung cancer patients for optimal therapy selection. In this study, we develop an artificial intelligence-powered spatial cellomics approach that combines histology, multiplex immunofluorescence imaging and multimodal machine learning to characterize the complex cellular relationships of 43 cell phenotypes in the tumor microenvironment in a real-world retrospective cohort of 1168 non-small cell lung cancer patients from two large German cancer centers. The model identifies cell niches associated with survival and achieves a 14% and 47% improvement in risk stratification in the two main non-small cell lung cancer subtypes, lung adenocarcinoma and squamous cell carcinoma, respectively, combining niche patterns with conventional cancer staging. Our results show that complex immune cell niche patterns identify potentially undertreated high-risk patients qualifying for adjuvant therapy. Our approach highlights the potential of artificial intelligence powered multiplex imaging analyses to better understand the contribution of the tumor microenvironment to cancer progression and to improve risk stratification and treatment selection in non-small cell lung cancer.