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Updated: Jul 10, 2026

In Vivo, Percutaneous, Needle Based, Optical Coherence Tomography of Renal Masses
Published on: March 30, 2015
Multimodal imaging to analyze the biomechanical properties of kidney tumors, evaluating feasibility, inter-modality
Mattia Ronca1,2, Paolo Conforti1,2, Amandine Crombé3,4
1Urology Department, Bordeaux University Hospital, Bordeaux, France.
Introduction:
Assessment of renal tissue and renal tumor stiffness may provide complementary information for tissue characterization; however, conventional imaging modalities such as multiphasic computed tomography (CT) do not directly quantify biomechanical properties. Elastography techniques, including magnetic resonance elastography (MRE) and ultrasound elastography (US-E), allow noninvasive measurement of tissue stiffness but are not routinely available in standard clinical practice. This study protocol aims to develop a CT-based stiffness mapping of renal parenchyma and renal tumors by investigating the relationship between CT attenuation values and elastography-derived stiffness measurements, using MRE and US-E as reference modalities.
Methods And Analysis:
This monocentric, prospective, exploratory, non-randomized, and non-blinded diagnostic study will enroll 50 adults undergoing partial or radical nephrectomy for renal tumors at the University Hospital of Bordeaux. All participants will undergo a predefined multimodal imaging protocol-including contrast-enhanced CT, multiparametric magnetic resonance imaging (MRI) with -MRE and US-E-conducted between inclusion and the day before surgery. The primary objective is to construct a regression model predicting MRE-derived elasticity (μMRE) from CT density values using multiple machine-learning algorithms evaluated through repeated nested cross-validation. Secondary analyses will include voxel-level and region-of-interest correlations across modalities, feasibility and image-quality assessment of DWI-vMRE, repeatability of elastography measurements, identification of limiting factors such as BMI, sarcopenia, lesion location and architecture, evaluation of inter-modality de-correlation and associations with final histopathology (including subtype and grade).
Trial Registration:
ClinicalTrials.gov identifier: NCT06525831. Protocol ID-RCB: 2024-A00959-38. Recruitment began on 7 March 2025.
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