External validation of the Uromonitor®-version 2 urine test as a biomarker for optimisation of non-muscle-invasive bladder cancer management
Rubio-Briones, José ; Guerrero Ramos, Félix ; Mercadé Sánchez, Asier ; Bezana Abadía, Inés ; Martín Rodríguez, Ruth ; Alcaraz, Antonio ; Miqueleiz Legaz, Maite ; Lozano, Fernando ; Arrabal Martín, Miguel ; Luis Cardo, Adrián ; Gonzalo Rodríguez, Victoria ; Caño Velasco, Jorge ; Serrano Liesa, Miriam ; Ferreiro Pareja, Cristina ; Espílez Ortiz, Raquel (Universidad de Zaragoza) ; González-Valcárcel de Torres, Ignacio de ; Sánchez Zalabardo, Daniel ; Esquinas, Cristina ; Mengual, Lourdes ; Borque-Fernando, Angel (Universidad de Zaragoza) ; Esteban Escaño, Luis Mariano ; Palou Redorta, Joan ; Witjes, Fred ; Martínez Piñeiro, Luis
Resumen: Objectives
To conduct an external multicentre validation to evaluate Uromonitor®‐version 2 (v2; U‐monitor, Porto, Portugal) as a biomarker for detecting non‐muscle‐invasive bladder cancer (NMIBC) recurrence in an independent patient cohort in a real‐world‐evidence setting and compare it to cytology.
Patients and Methods
The ‘External Validation of Uromonitor as a Biomarker for Optimization of NMIBC Management by the Club Urológico Español de Tratamiento Oncológico Group’ (EVALUATION‐CUETO) study is a prospective, multicentre, observational study (NCT05864599) conducted in Spain. Inclusion criteria included any risk group of patients with NMIBC undergoing follow‐up. The most recent (index) NMIBC tumours of any grade had to have been diagnosed within the past 3 months to 2 years. Regarding biomarkers, data from cystoscopy, cytology, and the Uromonitor‐v2 test were collected. Predictive performance parameters, including accuracy, area under the curve, negative and positive predictive values (NPV, PPV), sensitivity, and specificity, were calculated.
Results
A total of 1178 patients with a mean age of 72 years and a predominant male representation (80%) were included. Among the positive Uromonitor-v2 cases, 64 (57.66%) exhibited a TERT promoter mutation, and 59 (53.15%) harboured a FGFR3 mutation. No KRAS mutations were found. For the total population, Uromonitor-v2 demonstrated high specificity (0.93) and NPV (0.93), but low sensitivity (0.36) and PPV (0.36), indicating a limited ability to detect all recurrences and confirm positive cases. Performance varied across tumour grades, with low-grade tumours showing a low sensitivity of 0.32 and high-grade tumours achieving a higher but insufficient sensitivity of 0.44. Specificity remained consistent at 0.93 across all groups. Uromonitor-v2 achieved higher accuracy compared to cytology alone, with the combined approach further improving overall predictive performance.
Conclusion
The strong specificity and NPV observed across all studies suggest a role of Uromonitor‐v2 as a potential tool for NMIBC follow‐up, particularly in ruling out recurrence and clarifying doubtful cystoscopy results. However, the unexpectedly low sensitivity reported in this external multicentre validation suggests the need for further investigation before routine clinical implementation.
Idioma: Inglés
DOI: 10.1111/bju.70010
Año: 2025
Publicado en: BJU international (2025), [9 p.]
ISSN: 1464-4096
Tipo y forma: Artículo (Versión definitiva)
Área (Departamento): Área Urología (Dpto. Cirugía)
Derechos reservados por el editor de la revista
0
Exportado de SIDERAL (2025-11-13-14:58:47)
To conduct an external multicentre validation to evaluate Uromonitor®‐version 2 (v2; U‐monitor, Porto, Portugal) as a biomarker for detecting non‐muscle‐invasive bladder cancer (NMIBC) recurrence in an independent patient cohort in a real‐world‐evidence setting and compare it to cytology.
Patients and Methods
The ‘External Validation of Uromonitor as a Biomarker for Optimization of NMIBC Management by the Club Urológico Español de Tratamiento Oncológico Group’ (EVALUATION‐CUETO) study is a prospective, multicentre, observational study (NCT05864599) conducted in Spain. Inclusion criteria included any risk group of patients with NMIBC undergoing follow‐up. The most recent (index) NMIBC tumours of any grade had to have been diagnosed within the past 3 months to 2 years. Regarding biomarkers, data from cystoscopy, cytology, and the Uromonitor‐v2 test were collected. Predictive performance parameters, including accuracy, area under the curve, negative and positive predictive values (NPV, PPV), sensitivity, and specificity, were calculated.
Results
A total of 1178 patients with a mean age of 72 years and a predominant male representation (80%) were included. Among the positive Uromonitor-v2 cases, 64 (57.66%) exhibited a TERT promoter mutation, and 59 (53.15%) harboured a FGFR3 mutation. No KRAS mutations were found. For the total population, Uromonitor-v2 demonstrated high specificity (0.93) and NPV (0.93), but low sensitivity (0.36) and PPV (0.36), indicating a limited ability to detect all recurrences and confirm positive cases. Performance varied across tumour grades, with low-grade tumours showing a low sensitivity of 0.32 and high-grade tumours achieving a higher but insufficient sensitivity of 0.44. Specificity remained consistent at 0.93 across all groups. Uromonitor-v2 achieved higher accuracy compared to cytology alone, with the combined approach further improving overall predictive performance.
Conclusion
The strong specificity and NPV observed across all studies suggest a role of Uromonitor‐v2 as a potential tool for NMIBC follow‐up, particularly in ruling out recurrence and clarifying doubtful cystoscopy results. However, the unexpectedly low sensitivity reported in this external multicentre validation suggests the need for further investigation before routine clinical implementation.
Idioma: Inglés
DOI: 10.1111/bju.70010
Año: 2025
Publicado en: BJU international (2025), [9 p.]
ISSN: 1464-4096
Tipo y forma: Artículo (Versión definitiva)
Área (Departamento): Área Urología (Dpto. Cirugía)
Derechos reservados por el editor de la revista0
Exportado de SIDERAL (2025-11-13-14:58:47)
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Artículos > Artículos por área > Urología
Registro creado el 2025-11-13, última modificación el 2025-11-13