Development and deployment of a histopathology-based deep learning algorithm for patient prescreening in a clinical trial.
Albert Juan RamonChaitanya ParmarOscar M Carrasco-ZevallosCarlos CsiszerStephen S F YipPatricia RacitiNicole L StoneSpyros TriantosMichelle M QuirozPatrick CrowleyAshita S BataviaJoel GreshockTommaso MansiKristopher A StandishPublished in: Nature communications (2024)
Accurate identification of genetic alterations in tumors, such as Fibroblast Growth Factor Receptor, is crucial for treating with targeted therapies; however, molecular testing can delay patient care due to the time and tissue required. Successful development, validation, and deployment of an AI-based, biomarker-detection algorithm could reduce screening cost and accelerate patient recruitment. Here, we develop a deep-learning algorithm using >3000 H&E-stained whole slide images from patients with advanced urothelial cancers, optimized for high sensitivity to avoid ruling out trial-eligible patients. The algorithm is validated on a dataset of 350 patients, achieving an area under the curve of 0.75, specificity of 31.8% at 88.7% sensitivity, and projected 28.7% reduction in molecular testing. We successfully deploy the system in a non-interventional study comprising 89 global study clinical sites and demonstrate its potential to prioritize/deprioritize molecular testing resources and provide substantial cost savings in the drug development and clinical settings.
Keyphrases
- deep learning
- machine learning
- end stage renal disease
- clinical trial
- artificial intelligence
- convolutional neural network
- ejection fraction
- chronic kidney disease
- newly diagnosed
- prognostic factors
- peritoneal dialysis
- study protocol
- gene expression
- randomized controlled trial
- single molecule
- climate change
- quantum dots
- open label