Mattia Ronca

Dr. Mattia Ronca

orcid

Research Focus & Metrics

Academic Career Length

1Year (2026-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
13 August 2026 in Cancers
Verified
Journal Article
Open access
PDF file
FCFilippo Caudana
Filippo Caudana
MRMattia Ronca
Mattia Ronca
FDFrancesco Ditonno
Francesco Ditonno
GPGreta Pettenuzzo
Greta Pettenuzzo
Celeste ManfrediCeleste Manfredi
Celeste Manfredi
Alessandro AntonelliAlessandro Antonelli
Alessandro Antonelli
Background/Objectives: To compare perioperative, pathological, functional, and oncological outcomes of robot-assisted radical nephrectomy with inferior vena cava tumor thrombectomy (RARN-TT) versus open (ORN-TT) and laparoscopic (LRN-TT) approaches. Methods: PubMed, Scopus, and Web of Science were searched for studies of adults with renal cell carcinoma and Mayo/Neves level I–IV inferior vena cava tumor thrombus undergoing RARN-TT versus ORN-TT and/or LRN-TT. Risk ratios and mean differences with 95% confidence intervals were calculated using random effects models with restricted maximum-likelihood estimation. Results: Eight retrospective studies including 1781 patients were included: 221 underwent robotic surgery, 1411 open surgery, and 149 laparoscopic surgery. Compared with ORN-TT, RARN-TT was associated with lower estimated blood loss (mean difference −900.5 mL, 95% confidence interval −1234.0 to −566.9; p = 0.001), lower transfusion probability (risk ratio 0.395, 95% confidence interval 0.159–0.979; p = 0.046), and shorter hospital stay (mean difference −3.79 days, 95% confidence interval −4.83 to −2.76; p < 0.001). No significant differences were observed in operative time, intensive care unit stay, postoperative complications, perioperative mortality, pathological outcomes, or overall survival. Evidence for cancer-specific and progression-free survival was limited. Comparisons with LRN-TT were exploratory. Conclusions: RARN-TT may reduce blood loss, transfusion requirements, and hospital stay compared with ORN-TT, without evidence of worse perioperative, pathological, or survival outcomes. However, all studies were retrospective and affected by selection bias and heterogeneity. RARN-TT may be considered for selected patients at experienced centers, particularly for lower-level thrombi. Prospective multicenter studies stratified by thrombus level are needed.

8 July 2026 in PLOS ONE
Verified
Journal Article
Open access
PDF file
MRMattia Ronca
Mattia Ronca
PCPaolo Conforti
Paolo Conforti
ACAmandine Crombé
Amandine Crombé
MJManon Jaffredo
Manon Jaffredo
SRSolène Ricard
Solène Ricard
EJEva Jambon
Eva Jambon
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.