Division of Urologic Pathology, Inform Diagnostics, Irving, Texas.
Weiss School of Natural Sciences, Rice University, Houston, Texas.
Cancer Cytopathol. 2021 Feb;129(2):114-120. doi: 10.1002/cncy.22349. Epub 2020 Sep 15.
Urinary cytology is a noninvasive and cost-effective diagnostic and surveillance test in the clinical management of urothelial carcinoma (UC). The Paris System for Reporting Urinary Cytology (TPS), published in 2016, introduced definite diagnostic criteria aimed at improving performance in detecting high-grade UC (HGUC) and decreasing the indeterminate (atypical) diagnosis.
The authors retrospectively reviewed and compared urinary cytology diagnoses reported between January 2013 and December 2014 (pre-TPS, 7658 cases) and between May 2016 and April 2018 (post-TPS, 20,026 cases) to assess the influence of TPS in their practice. The time in between was used as a learning period. Follow-up information and correlation with the UroVysion fluorescence in situ hybridization test were obtained when available.
Urinary cytology diagnoses pre-TPS included negative for UC (NUC) (n = 5293; 69.2%), atypical urothelial cells (AUC) (n = 2227; 29%), and suspicious/positive for HGUC (SHGUC/HGUC) (n = 138; 1.8%). Diagnoses post-TPS included negative for HGUC (NHGUC) (n = 18,507; 92.4%), AUC (n = 1237; 6.2%), and SHGUC/HGUC (n = 282; 1.4%). Comparing the pre-TPS and post-TPS periods, AUC diagnoses decreased from 29% to 6.2% (P < .00001), and the specificity and positive predictive value of AUC to detect HGUC significantly improved from 49% to 86% (P < .00001) and from 9% to 39% (P = .002), respectively. The correlation of an AUC diagnosis with a positive UroVysion test improved from 17% to 38% (P < .00001), whereas overall use of the UroVysion test was decreased.
Implementation of TPS resulted in a significant reduction in AUC diagnoses that had a superior correlation with a subsequent biopsy and a UroVysion test, resulting in potential reductions in test use and medical cost.
尿细胞学检查是一种非侵入性、具有成本效益的诊断和监测试验,可用于临床管理尿路上皮癌(UC)。2016 年发表的巴黎尿细胞学报告系统(TPS)引入了明确的诊断标准,旨在提高检测高级别 UC(HGUC)的性能,并减少不确定(非典型)诊断。
作者回顾性比较了 2013 年 1 月至 2014 年 12 月(TPS 前,7658 例)和 2016 年 5 月至 2018 年 4 月(TPS 后,20026 例)的尿细胞学诊断,以评估 TPS 在他们实践中的影响。在此期间,作为学习期。在有随访信息和与 UroVysion 荧光原位杂交试验相关时,获得了这些信息。
TPS 前的尿细胞学诊断包括非 UC(NUC)(n=5293;69.2%)、非典型尿路上皮细胞(AUC)(n=2227;29%)和可疑/阳性高级别 UC(SHGUC/HGUC)(n=138;1.8%)。TPS 后的诊断包括非 HGUC(NHGUC)(n=18507;92.4%)、AUC(n=1237;6.2%)和 SHGUC/HGUC(n=282;1.4%)。与 TPS 前和 TPS 后期间相比,AUC 诊断从 29%下降到 6.2%(P<.00001),AUC 检测 HGUC 的特异性和阳性预测值分别从 49%提高到 86%(P<.00001)和从 9%提高到 39%(P=.002)。AUC 诊断与阳性 UroVysion 检测的相关性从 17%提高到 38%(P<.00001),而 UroVysion 检测的总体使用率降低。
TPS 的实施显著降低了 AUC 诊断的数量,而 AUC 诊断与随后的活检和 UroVysion 检测相关性更高,这可能会降低检测的使用和医疗成本。