Clinical performance of Bladder EpiCheck™ versus voided urine cytology for detecting recurrence of nonmuscle invasive bladder cancer: Systematic review and meta-analysis

Cho-Han Chiang MD, MMSc , Yu-Cheng Chang MD , Chun-Yu Peng MD , Shih-Syuan Wang MD , Aunchalee Jaroenlapnopparat MD , Jeff Chun Hao Wang MD , Chen Liang Jou MD , Pui-Un Tang MD , Yuan Ping Hsia MD , Cho-Hsien Chiang MD , Cho-Hung Chiang MD
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引用次数: 0

Abstract

Background

Nonmuscle invasive bladder cancer (NMIBC) has a favorable prognosis but has high propensity for recurrence. Recent development in one of the urinary biomarker tests, Bladder EpiCheck™, offers a noninvasive and accurate method to detect NMIBC recurrence. In this study, we aimed to compare the diagnostic performance of Bladder EpiCheck™ with urine cytology to detect NMIBC recurrence.

Methods

We performed a systematic review search through PubMed, Embase, Cochrane Central Register of Controlled Trials, Web of Science, and Scopus from inception to July 2023. Diagnostic accuracy was defined by sensitivity, negative predictive value (NPV), specificity, and positive predictive value (PPV).

Results

A total of 6 studies involving 1588 patients were included. Bladder EpiCheck™ has a sensitivity and specificity of 0.81 (95% CI: 0.63–0.91; I2: 43%) and 0.87 (95% CI: 0.83–0.91; I2: 20%), respectively. On the other hand, urine cytology has a sensitivity and specificity of 0.63 (95% CI: 0.29–0.87; I2: 61%) and 0.97 (95% CI: 0.78–1.00; I2: 79%), respectively. EpiCheck™ has a higher NPV (0.94 (95% CI: 0.87–0.97) vs. 0.84 (95% CI: 0.80–0.87) though a lower PPV (0.62 (95% CI: 0.45–0.76) vs. 0.87 (95% CI: 0.56–0.97) than urine cytology. In our subgroup analysis, the sensitivity of Bladder EpiCheck™ for detecting high-grade tumors improved to 0.90 (95% CI: 0.83–0.94) while that for urine cytology improved to 0.72 (95% CI: 0.50–0.87).

Conclusion

Bladder EpiCheck™ has a high sensitivity and NPV for detecting recurrence among patients with NMIBC.
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Bladder EpiCheck™ 与排空尿液细胞学在检测非肌层浸润性膀胱癌复发方面的临床表现:系统回顾与荟萃分析。
背景:非肌层浸润性膀胱癌(NMIBC)预后良好,但复发率高。最近开发的一种尿液生物标志物检测方法 Bladder EpiCheck™ 为检测 NMIBC 复发提供了一种无创、准确的方法。本研究旨在比较 Bladder EpiCheck™ 和尿液细胞学检测 NMIBC 复发的诊断性能:我们在 PubMed、Embase、Cochrane Central Register of Controlled Trials、Web of Science 和 Scopus 上进行了系统性综述检索,检索时间从开始到 2023 年 7 月。诊断准确性由灵敏度、阴性预测值(NPV)、特异性和阳性预测值(PPV)定义:结果:共纳入 6 项研究,涉及 1588 名患者。Bladder EpiCheck™ 的敏感性和特异性分别为 0.81(95% CI:0.63-0.91;I2:43%)和 0.87(95% CI:0.83-0.91;I2:20%)。另一方面,尿液细胞学检查的敏感性和特异性分别为 0.63(95% CI:0.29-0.87;I2:61%)和 0.97(95% CI:0.78-1.00;I2:79%)。EpiCheck™ 的 NPV(0.94(95% CI:0.87-0.97)对 0.84(95% CI:0.80-0.87))高于尿液细胞学检查,但 PPV(0.62(95% CI:0.45-0.76)对 0.87(95% CI:0.56-0.97)低于尿液细胞学检查。在我们的亚组分析中,膀胱EpiCheck™检测高级别肿瘤的灵敏度提高到0.90 (95% CI: 0.83-0.94),而尿液细胞学检测的灵敏度提高到0.72 (95% CI: 0.50-0.87):结论:膀胱 EpiCheck™ 对检测 NMIBC 患者的复发具有较高的灵敏度和 NPV。
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来源期刊
CiteScore
4.80
自引率
3.70%
发文量
297
审稿时长
7.6 weeks
期刊介绍: Urologic Oncology: Seminars and Original Investigations is the official journal of the Society of Urologic Oncology. The journal publishes practical, timely, and relevant clinical and basic science research articles which address any aspect of urologic oncology. Each issue comprises original research, news and topics, survey articles providing short commentaries on other important articles in the urologic oncology literature, and reviews including an in-depth Seminar examining a specific clinical dilemma. The journal periodically publishes supplement issues devoted to areas of current interest to the urologic oncology community. Articles published are of interest to researchers and the clinicians involved in the practice of urologic oncology including urologists, oncologists, and radiologists.
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State of the Art: The Microbiome in Bladder Cancer. Corrigendum to "A 2-center review of histopathology of variants of upper urinary tract urothelial carcinoma and their impact on clinical outcomes" [Urologic Oncology: Seminars and Original Investigations Volume 42 (2024) 333.e15-333.e20]. Laparoscopic suture-free partial nephrectomy using argon-beam-coagulator: Surgical technique and outcomes of a single-center, open-label randomized controlled trial. Editorial Board Table of Contents
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