ArticleNpj imaging2026
Dual deep learning approach for non-invasive renal tumour subtyping with VERDICT-MRI.
Article in Npj imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07173140 (A Two Site Pilot Study of Functional and Microstructural Imaging Using Magnetic Resonance Imaging in Patients With Renal Tumours), which is not on this map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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A Two Site Pilot Study of Functional and Microstructural Imaging Using Magnetic Resonance Imaging in Patients With Renal Tumours
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Authors and funding
9 authors.
Funding
Abstract
Renal cell carcinomas (RCCs) have multiple subtypes that are difficult to distinguish using imaging alone. This study characterises renal tumour microstructure using diffusion MRI (dMRI) and the Vascular, Extracellular and Restricted Diffusion for Cytometry in Tumours (VERDICT)-MRI framework. Patients were prospectively recruited from the RIM trial (ClinicalTrials.gov: NCT07173140, 20/11/2024). Fourteen patients with 17 renal tumours (including benign and various RCC subtypes) underwent dMRI using nine b-values (0-2500 s/mm²). A three-compartment VERDICT model was fitted with a self-supervised neural network. Compared to simpler dMRI models, VERDICT more accurately captured the diffusion data in tumour and healthy tissue. VERDICT revealed significant differences in intracellular volume fraction between cancerous and normal tissue, and in vascular volume fraction between vascular and non-vascular regions. A feature selection method identified a reduced 4 b-value protocol (b = [70, 150, 1000, 2000]), cutting scan time by over 30 min, enabling more efficient imaging in larger cohorts.
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