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Explainable AI Predicts Hematoxicity from Cancer Treatment Using Multimodal Real-World Data

Julius Keyl
Philipp Keyl
Tim Lenfers
René Hosch
Niklas Kiermeyer
Simon Schallenberg
Moon Kim
Sebastian Bauer
Nikolaos Bechrakis
Michael Forsting
Dagmar Führer-Sakel
Sied Kebir
Viktor Grünwald
Boris Hadaschik
Johannes Haubold
Ken Herrmann
Stefan Kasper
Rainer Kimmig
Stephan Lang
Tienush Rassaf
Alexander Roesch
Dirk Schadendorf
Jens T. Siveke
Martin Stuschke
Ulrich Sure
Matthias Totzeck
Anja Welt
Marcel Wiesweg
Jan Egger
Sylvia Hartmann
Grégoire Montavon
Felix Nensa
Klaus-Robert Müller
Martin Schuler
Jens Kleesiek
Frederick Klauschen

April 30, 2026

Adverse drug effects remain a major barrier to safe and effective cancer therapy, underscoring the need for tools that predict treatment-related toxicities. We analyzed multimodal real-world data from 14,596 cancer patients across 38 cancer entities, encompassing 330 clinical, tumor, and imaging characteristics, along with 89 anticancer agents. Hematological adverse events (HAE), defined by nadirs of hemoglobin, leukocyte, neutrophil, and platelet values within two months of treatment initiation, were highly prevalent (87.7%; 33.1% severe). We developed Toxix, an explainable artificial intelligence (xAI) framework modeling interactions between patient characteristics and drug combinations. Toxix achieved strong predictive performance for severe toxicities (median AUROC 0.85 for anemia; >0.76 for leukopenia, neutropenia, and thrombocytopenia) and was validated in an external cohort of 2,768 patients with non-small cell lung cancer. Model explainability enabled systematic characterization of drug-patient interactions underlying HAEs. Toxix provides a real-world informed framework for personalized and toxicity-aware cancer therapy planning.