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Unveiling the challenges of UTUC biopsies and cytology: insights from a global real-world practice study.
Baard, Joyce; Cormio, Luigi; Dasgupta, Ranan; Maruzzi, Daniele; Rais-Bahrami, Soroush; Serrano, Alvaro; Geavlete, Bogdan; Giannakopoulos, Stilianos; de la Rosette, Jean; Laguna, Pilar.
  • Baard J; Department of Urology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands. j.baard@amsterdamumc.nl.
  • Cormio L; Cancer Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands. j.baard@amsterdamumc.nl.
  • Dasgupta R; Department of Urology, University of Foggia, Foggia, Italy.
  • Maruzzi D; Department of Urology, Imperial College Healthcare NHS Trust, London, UK.
  • Rais-Bahrami S; Department of Urology, S. Maria Degli Angeli Hospital, Pordenone, Italy.
  • Serrano A; Departments of Urology and Radiology, O'Neal Comprehensive Cancer Center at UAB, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Geavlete B; Department of Urology, Hospital Clínico San Carlos, Madrid, Spain.
  • Giannakopoulos S; Department of Urology, Sanador Hospital, Bucharest, Romania.
  • de la Rosette J; Department of Urology, School of Medicine, Democritus University of Thrace, University Hospital of Alexandroupolis, Alexandroupolis, Greece.
  • Laguna P; Department of Urology, Istanbul Medipol Mega University Hospital, Istanbul Medipol University, Istanbul, Turkey.
World J Urol ; 42(1): 177, 2024 Mar 20.
Article en En | MEDLINE | ID: mdl-38507109
ABSTRACT

PURPOSE:

Diagnostic ureteroscopy (dURS) is optional in the assessment of patients with upper tract urothelial carcinoma (UTUC) and provides the possibility of obtaining histology.

METHODS:

To evaluate endoscopic biopsy techniques and outcomes, we assessed data from patients from the CROES-UTUC registry. The registry includes multicenter prospective collected data on diagnosis and management of patients suspected having UTUC.

RESULTS:

We assessed 2380 patients from 101 centers. dURS with biopsy was performed in 31.6% of patients. The quality of samples was sufficient for diagnosis in 83.5% of cases. There was no significant association between biopsy techniques and quality (p = 0.458). High-grade biopsy accurately predicted high-grade disease in 95.7% and high-risk stage disease in 86%. In ureteroscopic low-grade tumours, the prediction of subsequent low-grade disease was 66.9% and low-risk stage Ta-disease 35.8%. Ureteroscopic staging correctly predicted non-invasive Ta-disease and ≥ T1 disease in 48.9% and 47.9% of patients, respectively. Cytology outcomes did not provide additional value in predicting tumour grade.

CONCLUSION:

Biopsy results adequately predict high-grade and high-risk disease, but approximately one-third of patients are under-staged. Two-thirds of patients with low-grade URS-biopsy have high-risk stage disease, highlighting the need for improved diagnostics to better assess patient risk and guide treatment decisions. CLINICAL TRIAL REGISTRATION The study was registered at ClinicalTrials.gov (ClinicalTrials.gov NCT02281188; https//clinicaltrials.gov/ct2/show/NCT02281188 ).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ureterales / Neoplasias de la Vejiga Urinaria / Carcinoma de Células Transicionales / Neoplasias Renales Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ureterales / Neoplasias de la Vejiga Urinaria / Carcinoma de Células Transicionales / Neoplasias Renales Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article