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Conditional Diffusion Models for CT Image Synthesis from CBCT: A Systematic Review
Alzahra Altalib1,2, Chunhui Li1, Alessandro Perelli3
1School of Science and Engineering, University of Dundee, Dundee DD1 4HN, UK.
Background:
Cone Beam Computed Tomography (CBCT) is widely used in image-guided radiotherapy because it provides on-board volumetric imaging at relatively low doses, but its clinical utility for synthetic CT (sCT) generation remains limited by noise, scatter, artifacts, and reduced Hounsfield Unit (HU) fidelity. Conditional diffusion models (CDMs) have recently emerged as a promising alternative to earlier deep learning approaches because their iterative denoising process may better preserve anatomical structure and model uncertainty.
Objective:
This systematic review evaluates the use of conditional diffusion models for CBCT-to-CT synthesis, with particular attention to architectural strategies, reported quantitative outcomes, and potential clinical relevance. A systematic search was conducted in PubMed, Web of Science, Scopus, IEEE Xplore, and Google Scholar for studies published between 2013 and 2024. Eleven studies met the eligibility criteria and were analyzed to address three questions: (1) Which conditional diffusion strategies have been used? (2) What outcomes have been reported? and (3) What clinical implications have been discussed?
Results:
Across the included studies, CDMs frequently showed promising image quality performance, especially when incorporating anatomical priors, spatial-frequency guidance, hierarchical refinement, or latent representations. However, the evidence base remains small and highly heterogeneous with respect to anatomy, dimensionality, supervision strategy, and evaluation metrics, limiting the strength of direct comparative claims. The reviewed literature suggests that conditional diffusion models are a promising direction for CBCT-to-CT synthesis, but stronger dose-aware validation, standardized reporting, and broader multicenter evaluation are still needed before routine clinical deployment. This review has been registered with the International Prospective Register of Systematic Reviews (PROSPERO), under registration number CRD42024619240.
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