4.6 Article

A urine-based DNA methylation assay to facilitate early detection and risk stratification of bladder cancer

Journal

CLINICAL EPIGENETICS
Volume 13, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13148-021-01073-x

Keywords

Bladder cancer; DNA methylation assay; Early detection; Risk stratification

Funding

  1. National Key Research and Development Program of China [2017YFC1309002]
  2. Science and Technology Planning Project of Guangdong Province, China [2017B020226005]
  3. Scheme of Guangzhou Economic and Technological Development District for Leading Talents in Innovation and Entrepreneurship [2017-L152]
  4. Scheme of Guangzhou for Leading Talents in Innovation and Entrepreneurship [2016007]
  5. National Natural Science Foundation of China [82072827, 81825016, 81961128027, 81702523]
  6. Guangdong Basic and Applied Basic Research Foundation, China [2021B1515020009, 2020A1515010888]
  7. Science and Technology Program of Guangzhou, China [202102010002]
  8. Scheme of Guangzhou for Leading Team in Innovation [201909010010]

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The urine-based DNA methylation assay showed high sensitivities and specificities in detecting bladder cancer, especially in low-grade tumors and non-muscle invasive bladder cancer. It has potential to improve diagnosis and prognosis of bladder cancer in clinical settings.
BackgroundCurrent non-invasive tests have limited sensitivities and lack capabilities of pre-operative risk stratification for bladder cancer (BC) diagnosis. We aimed to develop and validate a urine-based DNA methylation assay as a clinically feasible test for improving BC detection and enabling pre-operative risk stratifications.MethodsA urine-based DNA methylation assay was developed and validated by retrospective single-center studies in patients of suspected BC in Cohort 1 (n=192) and Cohort 2 (n=98), respectively. In addition, a prospective single-center study in hematuria patient group (Cohort 3, n=174) was used as a second validation of the model.ResultsThe assay with a dual-marker detection model showed 88.1% and 91.2% sensitivities, 89.7% and 85.7% specificities in validation Cohort 2 (patients of suspected BC) and Cohort 3 (patients of hematuria), respectively. Furthermore, this assay showed improved sensitivities over cytology and FISH on detecting low-grade tumor (66.7-77.8% vs. 0.0-22.2%, 0.0-22.2%), Ta tumor (83.3% vs. 22.2-41.2%, 44.4-52.9%) and non-muscle invasive BC (NMIBC) (80.0-89.7% vs. 51.5-52.0%, 59.4-72.0%) in both cohorts. The assay also had higher accuracies (88.9-95.8%) in diagnosing cases with concurrent genitourinary disorders as compared to cytology (55.6-70.8%) and FISH (72.2-77.8%). Meanwhile, the assay with a five-marker stratification model identified high-risk NMIBC and muscle invasive BC with 90.5% sensitivity and 86.8% specificity in Cohort 2.ConclusionsThe urine-based DNA methylation assay represents a highly sensitive and specific approach for BC early-stage detection and risk stratification. It has a potential to be used as a routine test to improve diagnosis and prognosis of BC in clinic.

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