Clinical usability of an explainable AI decision support tool and evaluation of multimodal models in NSCLC

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Authors: Arsela Prelaj, V. Miskovic, Matteo Sacco, Alberto Ferrarin, Cristina Licciardello, Leonardo Provenzano, Margherita Favali, Ludovica Lerma, Aleksandra Zec, Andrea Spagnoletti, Monica Ganzinelli, Daniele Lorenzini
+88 more Beshoy Guirges, Luca Invernizzi, Cecilia Silvestri, Laura Mazzeo, Marco Meazza Prina, Giulia Corrao, Margherita Ruggirello, Andra Diana Dumitrascu, Rosa Maria Di Mauro, Dario Monzani, Gabriella Pravettoni, Michele Zanitti, Davide Wilfredo Attila Macocchi, Moreno Bruno Marino, Chiara Cavalli, Rebecca Romanò, Claudia Giani, Samuel G. Armato, Alessandra Esposito, Christine M. Bestvina, Maria Spector, Bogot R. Naama, Reham Basheer, Adi Lahiani Hafzadi, Laila C. Roisman, Iris Watermann, Marlen Szewczyk, Till Olchers, Heinz Richter, Constantin Blanke-Roeser, Costanza Siniscalchi, Anna Di Lello, Teresa Arangoa, Valentina Bartolomeo, Nikolaos Spathas, Evangelos Sarris, Elena Fountzilas, Aina Arbusà, Rocio Caro-Consuegra, Patricia Iranzo, Melissa Fernández-Pinto, José Rodríguez-Morató, Luca Agnelli, Mario Occhipinti, Marta Brambilla, Teresa Beninato, Claudia Proto, Sokol Kosta, Michele Pio Di Palma, Eliana Rulli, Stefan Steurer, Ronald Simon, Michael Willis, Giancarlo Pruneri, Filippo de Braud, Marcello Restelli, Enriqueta Felip, Nir Peled, Alexander T. Pearson, Helena Linardou, Martin Reck, Giuseppe Lo Russo, Francesco Trovò, Alessandra Pedrocchi, Marina Chiara Garassino, Paolo Ambrosini, Ghazal Farhikhteh, Sabina Sangaletti, Michele Borraccino, Claudia Agosta, Chiara Bonalume, Federica Corso, Roberta Serino, Eleonora Gusmaroli, Marta De Ponti, Giuseppe Nardo, Giulia Montelatici, Alessandra Russo, Giorgia Di Liberti, Stefano Natangelo, Simone Rota, Giuseppe Leone, Miriam Fink, Chiara Giangregorio, Emilia Ambrosini, Alessandro Chiesi, Erica Pietroluongo, Francesca Piazza
Cited by: 1
References: 34

Abstract

Abstract Despite a decade in, immunotherapy (IO) treatment selection in non-small cell lung cancer (NSCLC) remains largely guided by subgroup analyses and imperfect programmed death ligand 1 (PD-L1) and clinical scores. To our knowledge, I 3 LUNG ( NCT05537922 ) is currently the largest international, real-world, multimodal, artificial intelligence (AI)-based study, enrolling 2,396 patients. We integrated real-world clinical and blood (CB) data, computed tomography (CT) images, digital pathology (DP), and genomics into machine learning early fusion (MLEF) and deep learning intermediate fusion (DLIF) models. Machine learning (ML) and deep learning (DL) CB-only models achieved consistent performance across outcomes with area under the curve (AUC) up to 0.77 in the test (TEST) set. Performance drop in external validation (EXVAL) likely reflects population differences (AUC range: 0.55–0.72). AI models significantly surpassed PD-L1, Eastern Cooperative Oncology Group performance status (ECOG PS), neutrophil-to-lymphocyte ratio (NLR), lactate dehydrogenase (LDH) and Lung Immune Prognostic Index (LIPI) score in the independent TEST set. The clinical usability study showed that lung expert and nonexpert physicians improved their prediction with the explainable AI (XAI) ML CB-only based tool. Although multimodal integration with MLEF (CB+CT+DP) was associated with higher performance, its incremental benefit remains uncertain, not translated in TEST and EXVAL. The I 3 LUNG project is a pioneering framework showing the clinical usefulness of AI tools. A prospective validation of the decision support system (both CB and multimodal) is currently undergoing in more than 2,000 patients.

Fields of Study & Subjects

Radiomics and Machine Learning in Medical Imaging Cancer Immunotherapy and Biomarkers Lung Cancer Diagnosis and Treatment

Publication details

Journal / source
Nature Medicine
Publisher
Springer Science and Business Media LLC
Volume
32
Issue
9
Pages
3235–3247
Publication date
1 September 2026
Language
EN