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Urine-Based Liquid Biopsy May Perform Similarly to Urine Cytology in Detecting Urothelial Carcinoma


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Analysis of DNA copy number variants in the cells exfoliated in urine showed improved sensitivity and similar specificity in detecting urothelial carcinoma compared to urine cytology, according to results published by Zeng et al in Clinical Cancer Research.

“Urine cytology, which is widely used to screen for bladder cancer, has high specificity but lacks sensitivity, especially for low-grade cancers,” said study author Chuan-Liang Xu, MD, PhD, a urologist at Changhai Hospital in Shanghai, in a statement.

“Cystoscopy, while more accurate than cytology, is an invasive procedure with added costs and potential complications for the patient,” he added. “Therefore, an inexpensive, noninvasive test for the detection and monitoring of bladder cancer is an unmet clinical need.”

“The DNA isolated from urine-exfoliated cells, a complex cell mixture that potentially includes tumor cells shed from the lining of the bladder, can provide clues to the presence of bladder cancer,” explained study author Jia-Tao Ji, MD, PhD, a urologist at Shanghai Hudong Hospital. “Because copy number variants are a hallmark of many cancers, we developed an assay to detect copy number variant burden in the DNA from urine-exfoliated cells.”

Photo credit: Getty

Assay Details

The assay, called UroCAD, begins with a urine sample. Following urine sedimentation and DNA extraction, the sample is analyzed using low-coverage whole-genome sequencing. Because the assay relies on the detection of overall copy number variant burden, and not on the identification of specific genetic alterations, this cost-effective sequencing method is an ideal technique for sample analysis, noted Dr. Xu.

The researchers used samples from patients enrolled in an observational clinical trial in Shanghai that is evaluating the UroCAD assay. A total of 190 patients (126 with urothelial carcinoma, 64 without cancer) participated in the discovery phase; no significant copy number variant burden was detected in those without cancer. The researchers then developed a diagnostic model which incorporated all autosomal chromosomal changes in urine-exfoliated cells.

UroCAD Performance

In the discovery cohort, UroCAD identified urothelial carcinoma with a sensitivity and specificity of 82.5% and 96.9%, respectively.

The UroCAD assay was then evaluated in a validation cohort comprising 95 patients (56 with urothelial carcinoma, 39 without cancer). When compared with urine cytology, the researchers found that UroCAD had significantly higher sensitivity (80.4% vs 33.9%) and comparable specificity (94.9% vs 100%) for the detection of urothelial carcinoma. Further, in the seven patients whose low-grade tumors were confined to the epithelial layer of the bladder (pTa tumors), UroCAD had a sensitivity of 71.4%, while urine cytology had a sensitivity of 0%.

The sensitivity of UroCAD corresponded with tumor grade, as it could detect low-grade and high-grade urothelial carcinoma with a sensitivity of 60% and 86.6%, respectively. Further, the sensitivity of the test correlated with tumor size; the sensitivity of detection for tumors of 1 cm or less, tumors between 1 and 3 cm, and tumors greater than 3 cm was 66.7%, 72%, and 95.5%, respectively.

“The relatively lower sensitivity of UroCAD for the detection of lower-grade or smaller tumors is not unexpected, as these tumors are less likely to have abundant chromosomal alterations,” said Dr. Xu. “Ultimately, we believe that our assay could help to reduce the frequency of cystoscopy examination, but not…replace it.”

“For patients with hematuria or who have suspected urothelial carcinoma, UroCAD is a promising way to replace cytology and to reduce repeated cystoscopy examinations,” said Dr. Ji. The use of UroCAD for the surveillance of urothelial carcinoma is currently being evaluated in a clinical trial.  

The detection of copy number variant burden was correlated with the amount of epithelial cells present, suggesting that a lack of sufficient exfoliated cells may limit the assay, noted Dr. Xu.

Disclosure: This study was sponsored by grants from the Shanghai Sailing Program, a discipline development program plan in Changhai Hospital, the National Natural Science Foundation of China, the Technology Innovation Action Project of Science and Technology Commission of Shanghai City, the Shanghai Key Laboratory of Cell Engineering, the Project of Excellent Academic Leader of Science and Technology Committee of Shanghai City, the National Science and Technology Major Project, the Shanghai Clinical Medical Center of Urological Diseases Program, and the Department of Science & Technology of Jinan City. For full disclosures of the study authors, visit clincancerres.aacrjournals.org.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.
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