Urine Methylation Test for Urothelial Cancer Diagnosis and Surveillance

Importance Urothelial carcinoma (UC) is characterized by frequent recurrence, and accurate noninvasive tests remain needed for early detection and postoperative surveillance. Objective To develop and validate a urine-based assay targeting AL021918.2 and vimentin ( VIM ) methylation for UC detection and postoperative surveillance. Design, Setting, and Participants This prospective, blinded, multicenter diagnostic study was performed at 3 tertiary medical centers in China. Samples were collected between December 1, 2021, and June 25, 2025. Consecutively enrolled adults with UC, benign urinary diseases, or nonurothelial malignant disease were included in a single-center training cohort, a 3-center validation cohort, and a prospective surveillance cohort. The surveillance cohort had a median follow-up of 6 months, completed December 13, 2023. Exposure Urinary DNA methylation was assessed using quantitative methylation-specific polymerase chain reaction (PCR) analysis. Main Outcomes and Measures The primary outcomes were the sensitivity and specificity of the methylation assay for UC detection. Secondary outcomes included diagnostic performance according to tumor stage and grade and comparisons with urine cytology and fluorescence in situ hybridization (FISH). Results This analysis included a total of 2307 participants, consisting of 643 in the training cohort (median age, 64 [IQR, 56-71] years; 494 men [76.8%]), 1620 in the validation cohort (median age, 67 [IQR, 61-73] years; 1129 men [69.7%]), and 44 with UC in the surveillance cohort (median age, 62 [IQR, 59-72] years; 32 men [72.7%]). The assay demonstrated sensitivities of 91.2% (95% CI, 87.6%-93.9%) in the training cohort and 90.8% (95% CI, 88.4%-92.8%) in the validation cohort and specificities of 90.0% (95% CI, 85.9%-93.2%) in the training cohort and 93.2% (95% CI, 91.3%-94.7%) in the validation cohort. In the training and validation cohorts, sensitivity remained high for Ta UC (79.6% [95% CI, 64.3%-89.7%] and 84.3% [95% CI, 77.8%-89.2%], respectively) and low-grade UC (86.4% [95% CI, 77.0%-92.5%] and 82.5% [95% CI, 75.7%-87.8%], respectively). Compared with urine cytology and FISH, the methylation assay demonstrated higher sensitivity while maintaining comparable specificity. After surgery, urinary methylation results were negative in 30 of 32 patients (93.8%) with positive preoperative results. During surveillance, the assay detected all 9 recurrences with a median lead time of 4.5 (IQR, 1.5-5.5) months before clinical confirmation and remained negative in 29 of 35 patients (82.9%) without recurrence. Conclusions and Relevance In this diagnostic study, a noninvasive PCR-based assay showed high diagnostic accuracy for UC detection and identified all observed recurrences during surveillance. The assay may serve as an adjunct for UC diagnosis and postoperative surveillance. Trial Registration Chinese Clinical Trial Registry Identifier: ChiCTR2300078302

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Journal
JAMA Network Open
Published
2026-09-29
DOI
https://doi.org/10.1001/jamanetworkopen.2026.36786
Primary Topic
Bladder and Urothelial Cancer Treatments
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article
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article

Urine Methylation Test for Urothelial Cancer Diagnosis and Surveillance

Wencong Han, Weifeng Xu, Shengwei Xiong, Ninghan Feng et al.
JAMA Network Open
Bladder and Urothelial Cancer Treatments
article

Urine Methylation Test for Urothelial Cancer Diagnosis and Surveillance

Wencong Han, Weifeng Xu, Shengwei Xiong, Ninghan Feng, Qi Tang, Yucai Wu, Yuhui He, Tingting Li, Xiaoping Zhang, Yanqing Gong, Shiming He, Liqun Zhou, Zhihua Li, Xinfei Li, Lanlan Dong, Xuesong Li
article en

Abstract

Importance Urothelial carcinoma (UC) is characterized by frequent recurrence, and accurate noninvasive tests remain needed for early detection and postoperative surveillance. Objective To develop and validate a urine-based assay targeting AL021918.2 and vimentin ( VIM ) methylation for UC detection and postoperative surveillance. Design, Setting, and Participants This prospective, blinded, multicenter diagnostic study was performed at 3 tertiary medical centers in China. Samples were collected between December 1, 2021, and June 25, 2025. Consecutively enrolled adults with UC, benign urinary diseases, or nonurothelial malignant disease were included in a single-center training cohort, a 3-center validation cohort, and a prospective surveillance cohort. The surveillance cohort had a median follow-up of 6 months, completed December 13, 2023. Exposure Urinary DNA methylation was assessed using quantitative methylation-specific polymerase chain reaction (PCR) analysis. Main Outcomes and Measures The primary outcomes were the sensitivity and specificity of the methylation assay for UC detection. Secondary outcomes included diagnostic performance according to tumor stage and grade and comparisons with urine cytology and fluorescence in situ hybridization (FISH). Results This analysis included a total of 2307 participants, consisting of 643 in the training cohort (median age, 64 [IQR, 56-71] years; 494 men [76.8%]), 1620 in the validation cohort (median age, 67 [IQR, 61-73] years; 1129 men [69.7%]), and 44 with UC in the surveillance cohort (median age, 62 [IQR, 59-72] years; 32 men [72.7%]). The assay demonstrated sensitivities of 91.2% (95% CI, 87.6%-93.9%) in the training cohort and 90.8% (95% CI, 88.4%-92.8%) in the validation cohort and specificities of 90.0% (95% CI, 85.9%-93.2%) in the training cohort and 93.2% (95% CI, 91.3%-94.7%) in the validation cohort. In the training and validation cohorts, sensitivity remained high for Ta UC (79.6% [95% CI, 64.3%-89.7%] and 84.3% [95% CI, 77.8%-89.2%], respectively) and low-grade UC (86.4% [95% CI, 77.0%-92.5%] and 82.5% [95% CI, 75.7%-87.8%], respectively). Compared with urine cytology and FISH, the methylation assay demonstrated higher sensitivity while maintaining comparable specificity. After surgery, urinary methylation results were negative in 30 of 32 patients (93.8%) with positive preoperative results. During surveillance, the assay detected all 9 recurrences with a median lead time of 4.5 (IQR, 1.5-5.5) months before clinical confirmation and remained negative in 29 of 35 patients (82.9%) without recurrence. Conclusions and Relevance In this diagnostic study, a noninvasive PCR-based assay showed high diagnostic accuracy for UC detection and identified all observed recurrences during surveillance. The assay may serve as an adjunct for UC diagnosis and postoperative surveillance. Trial Registration Chinese Clinical Trial Registry Identifier: ChiCTR2300078302

JAMA Network OpenVol. 9(9)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking University (CN), China-Japan Friendship Hospital (CN), Peking Union Medical College Hospital (CN), Wuxi No.2 People's Hospital (CN), Wuhan Union Hospital (CN), Peking University First Hospital (CN), First Affiliated Hospital Zhejiang University (CN), Huazhong University of Science and Technology (CN), Zhejiang University (CN)
Good health and well-being
Openalex Percentile: Top 9%
Bladder and Urothelial Cancer Treatments
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