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

A. Prelaj V. Mišković Matteo Sacco A. Ferrarin C. Licciardello L. Provenzano M. Favali L. Lerma Aleksandra Zec A. Spagnoletti M. Ganzinelli Daniele Lorenzini B. Guirges L. Invernizzi C. Silvestri L. Mazzeo M. Prina G. Corrao M. Ruggirello A. Dumitrascu R. D. di Mauro D. Monzani Gabriella Pravettoni M. Zanitti D. Macocchi M. Marino Chiara Cavalli R. Romanò C. Giani Samuel G. Armato Alessandra Esposito C. Bestvina Maria Spector Bogot R. Naama R. Basheer A. L. Hafzadi L. Roisman I. Watermann M. Szewczyk T. Olchers Heinz Richter C. Blanke-Roeser Costanza Siniscalchi A. Di Lello Teresa Arangoa V. Bartolomeo N. Spathas E. Sarris Elena Fountzilas A. A. Roca R. Caro-Consuegra Patricia Iranzo M. Fernández-Pinto J. Rodríguez-Morató L. Agnelli M. Occhipinti M. Brambilla Teresa Beninato C. Proto S. Kosta M. Di Palma Eliana Rulli S. Steurer R. Simon Michael Willis G. Pruneri F. D. de Braud Marcello Restelli E. Felip N. Peled A. Pearson Helena Linardou Martin Reck G. L. Russo F. Trovo' A. Pedrocchi M. Garassino P. Ambrosini G. 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 S. Rota G. Leone Miriam Fink Chiara Giangregorio E. Ambrosini Alessandro Chiesi Erica Pietroluongo Francesca Piazza N. Bonnet V. Subbiah Julieta Pellarolo Jana Mandler Nadine Heuer-Olewinski Jana Sonnek Milena Schmidt Christopher Wirks Hartmut Richter Stefania Gkoura Eleni Aravantinou Ioanna Gazouli Ilaria Priano Laura Masfarré Pintó Aina De Torner Augusto Valdivia Núria Pardo G. Romero Mireia Soleda Halid Kayan Anniina Hentinen Valter Torri V. Sebri Giovanni Scoazec
Sep 2026 · Nature Medicine · Vol 32, pp. 3235 - 3247 · 1 citation · 40 references
Medicine

TL;DR

In a large international real-world study of non-small cell lung cancer, a multimodal explainable AI model outperformed established biomarkers for immunotherapy outcome prediction and improved physician decision-making.

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, I3LUNG (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 I3LUNG 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. In a large international real-world study of non-small cell lung cancer, a multimodal explainable AI model outperformed established biomarkers for immunotherapy outcome prediction and improved physician decision-making.

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