Comparison of 2 new real-time polymerase chain reaction-based urinary markers in the follow-up of patients with non-muscle-invasive bladder cancer.


Journal

Cancer cytopathology
ISSN: 1934-6638
Titre abrégé: Cancer Cytopathol
Pays: United States
ID NLM: 101499453

Informations de publication

Date de publication:
05 2020
Historique:
received: 29 10 2019
revised: 01 12 2019
accepted: 02 01 2020
pubmed: 25 1 2020
medline: 24 11 2020
entrez: 25 1 2020
Statut: ppublish

Résumé

The objective of the current study was to compare the diagnostic accuracy of 2 new real-time polymerase chain reaction-based urinary markers with each other and with urinary cytology, cystoscopy, and/or histology in patients being followed for non-muscle-invasive bladder cancer. A total of 487 patients were enrolled in the study. Patients were evaluated using voided urine cytology, the Xpert Bladder Cancer Monitor, the Bladder EpiCheck test, and white light cystoscopy. The overall sensitivity was 27.17% for cytology, 64.13% for the Bladder EpiCheck test, and 66.3% for the Xpert Bladder Cancer Monitor. The overall specificity was 98.82% for cytology, 82.06% for the Bladder EpiCheck test, and 76.47% for the Xpert Bladder Cancer Monitor. The negative predictive value was very similar for the 3 tests at 83.56% for cytology, 89.42% for the Bladder EpiCheck test, and 89.35% for the Xpert Bladder Cancer Monitor. When combined, the Bladder EpiCheck test and Xpert Bladder Cancer Monitor detected overall 79.35% of the tumors: 70.37% in low-grade and 92.11% in high-grade tumors. The Xpert Bladder Cancer Monitor and Bladder EpiCheck test were found to perform very well in terms of sensitivity. Together, the 2 tests detected approximately 92.11% of high-grade tumors. Their specificity was high but could not reach the excellent value of cytology. The negative predictive value was the same for both tests and was higher than that for cytology, especially when the tests were used together (92.24%). These 2 new tests hold promise as urinary biomarkers. They may be used in combination to maximize sensitivity in a less invasive way, thereby reducing invasiveness in the follow-up of patients with non-muscle-invasive bladder cancer and decreasing discomfort for the patients as well as complications and costs.

Sections du résumé

BACKGROUND
The objective of the current study was to compare the diagnostic accuracy of 2 new real-time polymerase chain reaction-based urinary markers with each other and with urinary cytology, cystoscopy, and/or histology in patients being followed for non-muscle-invasive bladder cancer.
METHODS
A total of 487 patients were enrolled in the study. Patients were evaluated using voided urine cytology, the Xpert Bladder Cancer Monitor, the Bladder EpiCheck test, and white light cystoscopy.
RESULTS
The overall sensitivity was 27.17% for cytology, 64.13% for the Bladder EpiCheck test, and 66.3% for the Xpert Bladder Cancer Monitor. The overall specificity was 98.82% for cytology, 82.06% for the Bladder EpiCheck test, and 76.47% for the Xpert Bladder Cancer Monitor. The negative predictive value was very similar for the 3 tests at 83.56% for cytology, 89.42% for the Bladder EpiCheck test, and 89.35% for the Xpert Bladder Cancer Monitor. When combined, the Bladder EpiCheck test and Xpert Bladder Cancer Monitor detected overall 79.35% of the tumors: 70.37% in low-grade and 92.11% in high-grade tumors.
CONCLUSIONS
The Xpert Bladder Cancer Monitor and Bladder EpiCheck test were found to perform very well in terms of sensitivity. Together, the 2 tests detected approximately 92.11% of high-grade tumors. Their specificity was high but could not reach the excellent value of cytology. The negative predictive value was the same for both tests and was higher than that for cytology, especially when the tests were used together (92.24%). These 2 new tests hold promise as urinary biomarkers. They may be used in combination to maximize sensitivity in a less invasive way, thereby reducing invasiveness in the follow-up of patients with non-muscle-invasive bladder cancer and decreasing discomfort for the patients as well as complications and costs.

Identifiants

pubmed: 31977131
doi: 10.1002/cncy.22246
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

341-347

Informations de copyright

© 2020 American Cancer Society.

Références

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Auteurs

Emanuela Trenti (E)

Department of Urology, Central Hospital of Bolzano, Bolzano, Italy.

Stefan Pycha (S)

Faculty of Medicine, Riga Stradins University, Riga, Latvia.

Christine Mian (C)

Department of Pathology, Central Hospital of Bolzano, Bolzano, Italy.

Christine Schwienbacher (C)

Department of Pathology, Central Hospital of Bolzano, Bolzano, Italy.

Esther Hanspeter (E)

Department of Pathology, Central Hospital of Bolzano, Bolzano, Italy.

Mona Kafka (M)

Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.

Giorgio Alfredo Spedicato (GA)

Data Science Management and Actuary, Unipol Group Analytics, Bologna, Italy.

Egils Vjaters (E)

Department of Urology, Riga Stradins University Hospital, Riga, Latvia.

Stephan Degener (S)

Department of Urology, Helios-Clinic Wuppertal, Witten Herdecke University, Wuppertal, Germany.

Armin Pycha (A)

Department of Urology, Central Hospital of Bolzano, Bolzano, Italy.
Medical School, Sigmund Freud Private University, Vienna, Austria.

Carolina D'Elia (C)

Department of Urology, Central Hospital of Bolzano, Bolzano, Italy.

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