同时使用膀胱Epicheck®和尿液细胞学检查可提高泌尿道病变诊断随访的敏感性和特异性:来自多机构队列的最新数据。

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Diseases (Basel, Switzerland) Pub Date : 2024-09-18 DOI:10.3390/diseases12090219
Ludovica Pepe, Vincenzo Fiorentino, Cristina Pizzimenti, Giuseppe Riganati, Mariausilia Franchina, Marina Micali, Fernanda Russotto, Antonio Ieni, Giovanni Tuccari, Guido Fadda, Francesco Pierconti, Maurizio Martini
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引用次数: 0

摘要

背景/目的:膀胱癌是一种常见的泌尿系统恶性肿瘤,尿液细胞学检查被广泛用于膀胱癌的筛查和随访。一种名为 Bladder Epicheck® (BE)的新型诊断工具正越来越多地用于监测非肌层浸润性膀胱癌(NMIBC)的复发情况。同时使用 BE 和尿液细胞学检查可提高膀胱肿瘤随访的诊断性能。方法:在这项多中心研究中,我们回顾性评估了 322 名高级别膀胱癌随访患者在六年内(2018 年 1 月至 2024 年 3 月)的数据。以组织学为金标准,计算了细胞学和BE的诊断性能及其组合。结果显示18例复发患者被诊断为高级别尿路上皮癌NMIBC,8例为低级别乳头状NMIBC,4例为原位癌(CIS)。细胞学分析正确识别了 30 例癌症中的 26 例,286 例被正确诊断为阴性结果。BE 能正确识别 30 例癌症中的 25 例,285 例被正确诊断为阴性结果。结合 BE 和尿液细胞学检查可正确识别 30 个癌瘤中的 29 个,289 个被正确诊断为阴性结果。结论:结合 BE 和细胞学检查是对高级别 NMIBC 患者进行随访诊断的最有效方法,可减少不必要的侵入性手术。
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The Simultaneous Use of Bladder Epicheck® and Urinary Cytology Can Improve the Sensitivity and Specificity of Diagnostic Follow-Up of Urothelial Lesions: Up-to-Date Data from a Multi-Institutional Cohort.

Background/Objectives: Bladder cancer is a prevalent urinary system malignancy and urinary cytology is widely used for its screening and follow-up. A novel diagnostic tool called Bladder Epicheck® (BE) is increasingly being used for monitoring the recurrence of non-muscle-invasive bladder cancer (NMIBC). The simultaneous use of BE and urinary cytology can increase the diagnostic performances in the follow-up of bladder neoplasms. Methods: In this multicenter study, we retrospectively evaluated the data of 322 patients in follow-up for a high-grade bladder carcinoma over a six-year period (from January 2018 to March 2024). The diagnostic performances of both cytology and BE and their combination were calculated using histology as gold standard. Results: Recurrences were diagnosed as high-grade urothelial carcinoma NMIBC in 18 cases, low-grade papillary NMIBC in 8 cases, and carcinoma in situ (CIS) in 4 cases. Cytological analysis correctly identified 26 out of 30 carcinomas, while 286 were correctly diagnosed as negative results. BE correctly identified 25 out of 30 carcinomas, 285 were correctly diagnosed as negative results. The combination of BE and urinary cytology correctly identified 29 out of 30 carcinomas, while 289 were correctly diagnosed as negative results. Conclusions: The combination of BE and cytology could be the most effective approach for follow-up diagnosis in patients with high-grade NMIBC, reducing unnecessary invasive procedures.

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