Literature DB >> 31060038

A Review of Urine Ancillary Tests in the Era of the Paris System.

Derek B Allison1, Christopher J VandenBussche2,3.   

Abstract

Aside from its diagnostic importance, urinary tract endoscopy is an uncomfortable, expensive, and time-consuming procedure. Patients with a history of urothelial carcinoma remain at an increased risk for recurrence and the development of de novo disease; most have had exposure to carcinogenic risk factors for decades prior to their first diagnosis that have bathed the entire urothelial tract. Consequently, monitoring these patients over their lifetime has made urothelial carcinoma one of the most expensive cancers for the US healthcare system. This expense has provided a financial incentive for academic and commercial groups to develop a test with a sufficient negative predictive value to reduce the frequency of surveillance procedures. Slide-based tests require a separate slide prepared from a split urine sample or from an additional urinary tract specimen. This process can place an additional burden on the laboratory due to changes in the workflow, especially if the split specimens need to be stored until a cytologic diagnosis is rendered (i.e., when used as a reflex test). Importantly, slide-based tests allow for the result to be directly correlated with cytomorphologic findings; however, these tests require the cells of interest to be present. Thus, slide-based tests suffer from the same sensitivity issues as urinary tract cytology. In contrast, slide-free tests do not require an additional slide to be prepared, and laboratory testing may be centralized to a core facility or performed on-site. Some tests detect the expression of altered or abnormally expressed subcellular material (proteins, DNA, etc.) in urothelial neoplasms, which are found in tumor cells and/or in the urine specimen when the proteins are either excreted or leaked from degenerating tumor cells. Slide-free tests may also be developed into point-of-care tests, meaning that the result may be available to the urologist but not to the cytopathologist. Since these proteins are often disassociated from the tumor cells that produce them, such tests may have a positive result even if tumor cells are absent in the tested specimen. Here we review critical concepts as well as several ancillary tests that have been developed for urinary tract specimens.
© 2019 S. Karger AG, Basel.

Entities:  

Keywords:  Ancillary testing; Bladder cancer; Urine; Urothelial carcinoma; Urothelial neoplasia

Mesh:

Substances:

Year:  2019        PMID: 31060038     DOI: 10.1159/000499027

Source DB:  PubMed          Journal:  Acta Cytol        ISSN: 0001-5547            Impact factor:   2.319


  4 in total

Review 1.  Toward urinary cell-free DNA-based treatment of urothelial carcinoma: a narrative review.

Authors:  Yujiro Hayashi; Kazutoshi Fujita
Journal:  Transl Androl Urol       Date:  2021-04

Review 2.  The Diagnostic Dilemma of Urothelial Tissue Fragments in Urinary Tract Cytology Specimens.

Authors:  Derek B Allison; M Lisa Zhang; Poonam Vohra; Christopher J VandenBussche
Journal:  Diagnostics (Basel)       Date:  2022-04-08

3.  Moesin (MSN) as a Novel Proteome-Based Diagnostic Marker for Early Detection of Invasive Bladder Urothelial Carcinoma in Liquid-Based Cytology.

Authors:  Jeong Hwan Park; Cheol Lee; Dohyun Han; Jae Seok Lee; Kyung Min Lee; Min Ji Song; Kwangsoo Kim; Heonyi Lee; Kyung Chul Moon; Youngsoo Kim; Minsun Jung; Ji Hye Moon; Hyebin Lee; Han Suk Ryu
Journal:  Cancers (Basel)       Date:  2020-04-21       Impact factor: 6.639

Review 4.  Diagnostic performance of nuclear matrix protein 22 and urine cytology for bladder cancer: A meta-analysis.

Authors:  Jie Wang; Xi Zhao; Xiao Lei Jiang; Dong Lu; Qiang Yuan; Jiabing Li
Journal:  Diagn Cytopathol       Date:  2022-03-24       Impact factor: 1.390

  4 in total

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