Evidence map›Paper›PMID 42421607›Full record

ArticleCancer cytopathology2026

Keratin 17 immunocytochemistry in urine cytology for urothelial carcinoma detection: Diagnostic performance and interobserver agreement in a prospective real-world cohort.

Gregor Barth, Stefan Koch, Thorsten H Ecke

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Article in Cancer cytopathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Gregor BarthDepartment of Hematology, Oncology and Palliative Care, University Hospital Brandenburg, Brandenburg Medical School Theodor Fontane, Brandenburg, Germany.ORCID https://orcid.org/0000-0002-9423-9869
Stefan KochFaculty of Health Sciences Brandenburg, Brandenburg, Germany.ORCID https://orcid.org/0000-0001-5918-8472
Thorsten H EckeDepartment of Urology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.ORCID https://orcid.org/0000-0002-0787-2763

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUrine cytology is recommended for noninvasive detection of urothelial carcinoma (UC) but shows limited sensitivity, particularly in low-grade disease. Keratin 17 (K17) has emerged as a promising immunocytochemical marker. This study evaluated the diagnostic performance and interobserver agreement of K17 in a routine setting.

methodsThis prospective cross-sectional study included 184 urine samples from patients undergoing diagnostic evaluation for suspected UC. K17 immunocytochemistry was performed with a fully automated platform and independently evaluated by two blinded raters. Cytology was classified according to The Paris System for Reporting Urinary Cytology. UC status was determined by histology when available or by follow-up and multidisciplinary assessment. Diagnostic accuracy was assessed by receiver operating characteristic (ROC) analysis; interobserver reliability was assessed with the Cohen κ and intraclass correlation coefficient (ICC). Multivariable logistic regression evaluated combined diagnostic approaches.

resultsK17 expression was significantly higher in UC than in non-UC samples (p < .001). Across raters, area under the ROC curve (AUC) values ranged from 0.68 to 0.71. Sensitivity was 52.9%-65.9%, with a specificity of 73.7%-82.8%. Sensitivity ranged from 45.5% to 54.5% for low-grade tumors and from 57.7% to 73.1% for high-grade tumors. In stage-based analyses, sensitivity was 49.2%-61.5% for non-muscle-invasive UC and 65%-80% for muscle-invasive UC. Combining K17 with cytology numerically improved diagnostic discrimination (AUC value, 0.76; 95% CI, 0.69-0.83). Interobserver agreement was moderate to substantial (κ = 0.684; ICC, 0.653). Limitations included single-center design, partial histological verification (81%), and post hoc optimized cutoffs.

conclusionsK17 immunocytochemistry is a reproducible adjunct to urine cytology, with moderate diagnostic performance. It may warrant further evaluation as an adjunctive marker, particularly in low-grade and cytologically equivocal cases.

Indexed as

Biomarkers, TumorCarcinoma, Transitional CellKeratin-17Urinary Bladder NeoplasmsAgedAged, 80 and overCross-Sectional StudiesCytodiagnosisFemaleHumansImmunohistochemistryMaleMiddle AgedObserver VariationProspective StudiesReproducibility of ResultsBiomarkers, TumorKeratin-17KRT17 protein, humanAB_563797biomarkerscarcinomacytodiagnosisimmunocytochemistrykeratin 17tumorsurinary bladder neoplasms

Identifiers

PMID42421607
PMCPMC13421027

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.