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Autores principales: Mantegna, Massimiliano, Ayllón, Elena Mulero, Caragliano, Alice Natalina, Di Feola, Francesco, Tacconi, Claudia, Fiore, Michele, Ippolito, Edy, Greco, Carlo, Ramella, Sara, Cattin, Philippe C., Soda, Paolo, Tortora, Matteo, Guarrasi, Valerio
Formato: Preprint
Publicado: 2026
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Acceso en línea:https://arxiv.org/abs/2603.06147
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author Mantegna, Massimiliano
Ayllón, Elena Mulero
Caragliano, Alice Natalina
Di Feola, Francesco
Tacconi, Claudia
Fiore, Michele
Ippolito, Edy
Greco, Carlo
Ramella, Sara
Cattin, Philippe C.
Soda, Paolo
Tortora, Matteo
Guarrasi, Valerio
author_facet Mantegna, Massimiliano
Ayllón, Elena Mulero
Caragliano, Alice Natalina
Di Feola, Francesco
Tacconi, Claudia
Fiore, Michele
Ippolito, Edy
Greco, Carlo
Ramella, Sara
Cattin, Philippe C.
Soda, Paolo
Tortora, Matteo
Guarrasi, Valerio
contents Predicting tumor evolution during radiotherapy is a clinically critical challenge, particularly when longitudinal changes are driven by both anatomy and treatment. In this work, we introduce a Virtual Treatment (VT) framework that formulates non-small cell lung cancer (NSCLC) progression as a dose-aware multimodal conditional image-to-image translation problem. Given a CT scan, baseline clinical variables, and a specified radiation dose increment, VT aims to synthesize plausible follow-up CT images reflecting treatment-induced anatomical changes. We evaluate the proposed framework on a longitudinal dataset of 222 stage III NSCLC patients, comprising 895 CT scans acquired during radiotherapy under irregular clinical schedules. The generative process is conditioned on delivered dose increments together with demographic and tumor-related clinical variables. Representative GAN-based and diffusion-based models are benchmarked across 2D and 2.5D configurations. Quantitative and qualitative results indicate that diffusion-based models benefit more consistently from multimodal, dose-aware conditioning and produce more stable and anatomically plausible tumor evolution trajectories than GAN-based baselines, supporting the potential of VT as a tool for in-silico treatment monitoring and adaptive radiotherapy research in NSCLC.
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spellingShingle Longitudinal NSCLC Treatment Progression via Multimodal Generative Models
Mantegna, Massimiliano
Ayllón, Elena Mulero
Caragliano, Alice Natalina
Di Feola, Francesco
Tacconi, Claudia
Fiore, Michele
Ippolito, Edy
Greco, Carlo
Ramella, Sara
Cattin, Philippe C.
Soda, Paolo
Tortora, Matteo
Guarrasi, Valerio
Computer Vision and Pattern Recognition
Predicting tumor evolution during radiotherapy is a clinically critical challenge, particularly when longitudinal changes are driven by both anatomy and treatment. In this work, we introduce a Virtual Treatment (VT) framework that formulates non-small cell lung cancer (NSCLC) progression as a dose-aware multimodal conditional image-to-image translation problem. Given a CT scan, baseline clinical variables, and a specified radiation dose increment, VT aims to synthesize plausible follow-up CT images reflecting treatment-induced anatomical changes. We evaluate the proposed framework on a longitudinal dataset of 222 stage III NSCLC patients, comprising 895 CT scans acquired during radiotherapy under irregular clinical schedules. The generative process is conditioned on delivered dose increments together with demographic and tumor-related clinical variables. Representative GAN-based and diffusion-based models are benchmarked across 2D and 2.5D configurations. Quantitative and qualitative results indicate that diffusion-based models benefit more consistently from multimodal, dose-aware conditioning and produce more stable and anatomically plausible tumor evolution trajectories than GAN-based baselines, supporting the potential of VT as a tool for in-silico treatment monitoring and adaptive radiotherapy research in NSCLC.
title Longitudinal NSCLC Treatment Progression via Multimodal Generative Models
topic Computer Vision and Pattern Recognition
url https://arxiv.org/abs/2603.06147