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A Urine-based Genomic Assay Improves Risk Stratification for Patients with High-risk Hematuria Stratified According to the American Urological Association Guidelines.
de Jong, Joep J; Pijpers, Olga M; van Kessel, Kim E M; Boormans, Joost L; Van Criekinge, Wim; Zwarthoff, Ellen C; Lotan, Yair.
Afiliação
  • de Jong JJ; Department of Urology, Erasmus MC Urothelial Cancer Research Group, Rotterdam, The Netherlands. Electronic address: j.j.dejong@erasmusmc.nl.
  • Pijpers OM; Department of Urology, Erasmus MC Urothelial Cancer Research Group, Rotterdam, The Netherlands.
  • van Kessel KEM; Department of Urology, Erasmus MC Urothelial Cancer Research Group, Rotterdam, The Netherlands.
  • Boormans JL; Department of Urology, Erasmus MC Urothelial Cancer Research Group, Rotterdam, The Netherlands.
  • Van Criekinge W; Laboratory of Bioinformatics and Computational Genomics, Ghent University, Ghent, Belgium.
  • Zwarthoff EC; Department of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Lotan Y; Department of Urology, UT Southwestern Medical Center, Dallas, TX, USA.
Eur Urol Oncol ; 6(2): 183-189, 2023 04.
Article em En | MEDLINE | ID: mdl-36089502
ABSTRACT

BACKGROUND:

According to the recent American Urological Association (AUA) guideline on hematuria, patients are stratified into groups with low, intermediate, and high risk of urothelial carcinoma (UC). These risk groups are based on clinical factors and do not incorporate urine-based tumor markers.

OBJECTIVE:

To evaluate whether a urine-based genomic assay improves the redefined AUA risk stratification for hematuria. DESIGN, SETTING, AND

PARTICIPANTS:

We selected patients with complete biomarker status, as assessed on urinary DNA, from a previously collected prospective Dutch hematuria cohort (n = 838). Patients were stratified into the AUA risk categories on the basis of sex, age, and type of hematuria. Biomarker status included mutation status for the FGFR3, TERT, and HRAS genes, and methylation status for the OTX1, ONECUT2, and TWIST1 genes. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

The primary endpoint was the diagnostic model performance for different hematuria risk groups. Further analyses assessed the pretest and post-test UC probability in the hematuria subgroups using a Fagan nomogram. RESULTS AND

LIMITATIONS:

Overall, 65 patients (7.8%) were classified as low risk, 106 (12.6%) as intermediate risk, and 667 (79.6%) as high risk. The UC incidence differed significantly between the gross hematuria (21%, 98/457) and microscopic hematuria (4%, 14/381) groups (p < 0.001). All cancer cases were in the high-risk group, which had UC incidence of 16.8% (112/667). Application of the diagnostic model revealed robust performance among all risk groups (area under the receiver operating characteristic curve 0.929-0.971). Depending on the risk group evaluated, a negative urine assay was associated with post-test UC probability of 0.3-2%, whereas a positive urine assay was associated with post-test UC probability of 31-42%.

CONCLUSIONS:

This study shows the value that a urine-based genomic assay adds to the AUA guideline stratification for patients with hematuria. It seems justified to safely withhold cystoscopy for patients with AUA low risk who have a negative urine assay. In addition, evaluation should be expedited for patients with AUA intermediate or high risk and a positive urine assay. PATIENT

SUMMARY:

Patients who have blood in their urine (hematuria) can be classified as having low, intermediate, or high risk of having cancer in their urinary tract. We found that use of a urine-based genetic test improves the accuracy of predicting which patients are most likely to have cancer. Patients with a negative test may be able to avoid invasive tests, while further tests could be prioritized for patients with a positive test.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Carcinoma de Células de Transição Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Eur Urol Oncol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Carcinoma de Células de Transição Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Eur Urol Oncol Ano de publicação: 2023 Tipo de documento: Article