Diagnostic performance of Oncuria™, a urinalysis test for bladder cancer.


Journal

Journal of translational medicine
ISSN: 1479-5876
Titre abrégé: J Transl Med
Pays: England
ID NLM: 101190741

Informations de publication

Date de publication:
06 04 2021
Historique:
received: 19 02 2021
accepted: 18 03 2021
entrez: 7 4 2021
pubmed: 8 4 2021
medline: 15 5 2021
Statut: epublish

Résumé

Due to insufficient accuracy, urine-based assays currently have a limited role in the management of patients with bladder cancer. The identification of multiplex molecular signatures associated with disease has the potential to address this deficiency and to assist with accurate, non-invasive diagnosis and monitoring. To evaluate the performance of Oncuria™, a multiplex immunoassay for bladder detection in voided urine samples. The test was evaluated in a multi-institutional cohort of 362 prospectively collected subjects presenting for bladder cancer evaluation. The parallel measurement of 10 biomarkers (A1AT, APOE, ANG, CA9, IL8, MMP9, MMP10, PAI1, SDC1 and VEGFA) was performed in an independent clinical laboratory. The ability of the test to identify patients harboring bladder cancer was assessed. Bladder cancer status was confirmed by cystoscopy and tissue biopsy. The association of biomarkers and demographic factors was evaluated using linear discriminant analysis (LDA) and predictive models were derived using supervised learning and cross-validation analyses. Diagnostic performance was assessed using ROC curves. The combination of the 10 biomarkers provided an AUROC 0.93 [95% CI 0.87-0.98], outperforming any single biomarker. The addition of demographic data (age, sex, and race) into a hybrid signature improved the diagnostic performance AUROC 0.95 [95% CI 0.90-1.00]. The hybrid signature achieved an overall sensitivity of 0.93, specificity of 0.93, PPV of 0.65 and NPV of 0.99 for bladder cancer classification. Sensitivity values of the diagnostic panel for high-grade bladder cancer, low-grade bladder cancer, MIBC and NMIBC were 0.94, 0.89, 0.97 and 0.93, respectively. Urinary levels of a biomarker panel enabled the accurate discrimination of bladder cancer patients and controls. The multiplex Oncuria™ test can achieve the efficient and accurate detection and monitoring of bladder cancer in a non-invasive patient setting.

Sections du résumé

BACKGROUND
Due to insufficient accuracy, urine-based assays currently have a limited role in the management of patients with bladder cancer. The identification of multiplex molecular signatures associated with disease has the potential to address this deficiency and to assist with accurate, non-invasive diagnosis and monitoring.
METHODS
To evaluate the performance of Oncuria™, a multiplex immunoassay for bladder detection in voided urine samples. The test was evaluated in a multi-institutional cohort of 362 prospectively collected subjects presenting for bladder cancer evaluation. The parallel measurement of 10 biomarkers (A1AT, APOE, ANG, CA9, IL8, MMP9, MMP10, PAI1, SDC1 and VEGFA) was performed in an independent clinical laboratory. The ability of the test to identify patients harboring bladder cancer was assessed. Bladder cancer status was confirmed by cystoscopy and tissue biopsy. The association of biomarkers and demographic factors was evaluated using linear discriminant analysis (LDA) and predictive models were derived using supervised learning and cross-validation analyses. Diagnostic performance was assessed using ROC curves.
RESULTS
The combination of the 10 biomarkers provided an AUROC 0.93 [95% CI 0.87-0.98], outperforming any single biomarker. The addition of demographic data (age, sex, and race) into a hybrid signature improved the diagnostic performance AUROC 0.95 [95% CI 0.90-1.00]. The hybrid signature achieved an overall sensitivity of 0.93, specificity of 0.93, PPV of 0.65 and NPV of 0.99 for bladder cancer classification. Sensitivity values of the diagnostic panel for high-grade bladder cancer, low-grade bladder cancer, MIBC and NMIBC were 0.94, 0.89, 0.97 and 0.93, respectively.
CONCLUSIONS
Urinary levels of a biomarker panel enabled the accurate discrimination of bladder cancer patients and controls. The multiplex Oncuria™ test can achieve the efficient and accurate detection and monitoring of bladder cancer in a non-invasive patient setting.

Identifiants

pubmed: 33823873
doi: 10.1186/s12967-021-02796-4
pii: 10.1186/s12967-021-02796-4
pmc: PMC8025333
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

141

Subventions

Organisme : NCI NIH HHS
ID : R01 CA198887
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA206584
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA1988887
Pays : United States

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Auteurs

Yosuke Hirasawa (Y)

Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, Los Angeles, CA, USA.

Ian Pagano (I)

Cancer Prevention and Control Program, University of Hawaii Cancer Center, Honolulu, HI, USA.

Runpu Chen (R)

Department of Microbiology and Immunology, The State University of New York at Buffalo, Buffalo, NY, USA.

Yijun Sun (Y)

Department of Microbiology and Immunology, The State University of New York at Buffalo, Buffalo, NY, USA.

Yunfeng Dai (Y)

Department of Epidemiology, University of Florida, Gainesville, FL, USA.

Amit Gupta (A)

Division of Urology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

Sergei Tikhonenkov (S)

Translational and Clinical Program, University of Hawaii Cancer Center, Honolulu, HI, USA.

Steve Goodison (S)

Quantitative Health Sciences, Mayo Clinic Florida, Jacksonville, FL, USA.

Charles J Rosser (CJ)

Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, Los Angeles, CA, USA. rosser@nonagen.com.
Nonagen Bioscience Corp., Los Angeles, CA, USA. rosser@nonagen.com.

Hideki Furuya (H)

Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute, Los Angeles, CA, USA.

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Classifications MeSH