Imaging modalities for characterising T1 renal tumours: A systematic review and meta‐analysis of diagnostic accuracy

Author:

Warren Hannah12ORCID,Fanshawe Jack B.3ORCID,Mok Valerie4,Iyer Priyanka5,Chan Vinson Wai‐Shun6,Hesketh Richard7,Zimmermann Eleanor8,Kasivisvanathan Veeru1,Emberton Mark1ORCID,Tran Maxine G. B.12ORCID,Gurusamy Kurinchi1

Affiliation:

1. Division of Surgery and Interventional Science University College London London UK

2. Royal Free Hospital Specialist Centre for Kidney Cancer London UK

3. Guy's & St Thomas' NHS Foundation Trust London UK

4. Faculty of Medicine University of British Columbia Vancouver Canada

5. Guy's, King's and St Thomas' School of Medical Education King's College London London UK

6. School of Medicine University of Leeds Leeds UK

7. Centre of Medical Imaging A University College London London UK

8. University Hospitals Plymouth Plymouth UK

Abstract

AbstractObjectivesInternational guidelines recommend resection of suspected localised renal cell carcinoma (RCC), with surgical series showing benign pathology in 30%. Non‐invasive diagnostic tests to differentiate benign from malignant tumours are an unmet need. Our objective was to determine diagnostic accuracy of imaging modalities for detecting cancer in T1 renal tumours.MethodsA systematic review was performed for reports of diagnostic accuracy of any imaging test compared to a reference standard of histopathology for T1 renal masses, from inception until January 2023. Twenty‐seven publications (including 2277 tumours in 2044 participants) were included in the systematic review, and nine in the meta‐analysis.ResultsForest plots of sensitivity and specificity were produced for CT (seven records, 1118 participants), contrast‐enhanced ultrasound (seven records, 197 participants), [99mTc]Tc‐sestamibi SPECT/CT (five records, 263 participants), MRI (three records, 220 participants), [18F]FDG PET (four records, 43 participants), [68Ga]Ga‐PSMA‐11 PET (one record, 27 participants) and [111In]In‐girentuximab SPECT/CT (one record, eight participants). Meta‐analysis returned summary estimates of sensitivity and specificity for [99mTc]Tc‐sestamibi SPECT/CT of 88.6% (95% CI 82.7%–92.6%) and 77.0% (95% CI 63.0%–86.9%) and for [18F]FDG PET 53.5% (95% CI 1.6%–98.8%) and 62.5% (95% CI 14.0%–94.5%), respectively. A comparison hierarchical summary receiver operating characteristic (HSROC) model did not converge. Meta‐analysis was not performed for other imaging due to different thresholds for test positivity.ConclusionThe optimal imaging strategy for T1 renal masses is not clear. [99mTc]Tc‐sestamibi SPECT/CT is an emerging tool, but further studies are required to inform its role in clinical practice. The field would benefit from standardisation of diagnostic thresholds for CT, MRI and contrast‐enhanced ultrasound to facilitate future meta‐analyses.

Funder

Kidney and Urology Foundation of America

Publisher

Wiley

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