Cxbladder is a suite of genomic urine tests optimised for the rule-out and surveillance of urothelial cancer in patients presenting with haematuria and those being monitored for recurrent disease. The tests help you prioritise your time and clinical resources, optimise your practice workflow, and improve the overall patient experience.

  • Enables reliable risk stratification. Safely de-intensifies clinical workup in low risk patients, while prioritising higher risk patients for immediate care. 
  • Helps resolve atypical cytology and equivocal cystoscopy.
  • Offers a non-invasive surveillance alternative that can reduce the burden of repeated cystoscopy in those with a low risk of recurrence, improving comfort and compliance.


Cxbladder works at a molecular level, analysing five biomarker genes to help rule out urothelial cancer.

  • Objective and reliable: Exceptional performance and clinically actionable results. 
  • Clinically proven: Proven performance in over 20 peer-reviewed publications for primary detection and surveillance. Cxbladder has been used by over 4,400 US urologists in more than 100,000 patients. In New Zealand, the test is now available to 75% of the population through public healthcare.
  • Easy-to-use: Cxbladder’s unique urine sample collection system is non-invasive and easy for both clinical teams and patients to use.
  • Quick: Upon receiving a urine sample, our certified laboratory will provide actionable results in 7-10 business days.

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A Suite of Tests Optimised for Hematuria Evaluation and Surveillance

 

Haematuria Evaluation


Cxbladder Triage

Cxbladder Triage is a diagnostic test optimised for primary care. With high NPV, the test helps to de-intensify clinical work-up in haematuria patients with a low probability of urothelial cancer, reducing the need for referral and invasive procedures, while prioritising those who require further investigation.

  • Analyses gene expression alongside information on known UC risk factors like age, gender and smoking history to help rule out hematuria patients with a low risk of disease, while prioritising those who require further investigation.
  • Supports a new model for clinical practice and resource utilisation. This deployment model provides care to the greatest number of patients and offers clinically actionable information at the earliest point in the patient care pathway.

Cxbladder Detect

Cxbladder Detect is designed to improve practice workflow and efficiency, while giving patients the best experience possible. The test is optimised for the rule out of urothelial cancer in patients presenting with haematuria.

  • Enables reliable risk stratification. Safely de-intensifies clinical workup in low-risk patients, while prioritising higher risk patients for immediate care.
  • Spares low risk patients the discomfort, anxiety and risks of an invasive procedure.
  • Helps resolve diagnostic dilemmas like atypical cytology and equivocal cystoscopy.

 

Surveillance


Cxbladder Monitor

Cxbladder Monitor is a non-invasive surveillance alternative that can reduce the burden of repeated cystoscopy in non-muscle invasive bladder cancer patients with a low risk of recurrence, improving patient comfort and compliance.

  • In suitable cases post, can alternate with cystoscopy to de-intensify surveillance.
  • May be used to replace cystoscopy in patients with no recurrence long term after shared decision making with the patient.

Contact Us to Learn More About the Cxbladder Suite

 

Featured Videos: 


Ground Round in Urology: Use of the Cxbladder Monitor Genomic Urine  Test for Surveillance of Patients with Non-Muscle-Invasive Bladder Cancer. Click here to view.

GRU Video Graphic

 

UroToday: From Science to Clinical Utility

  • Cxbladder Detect - Bladder Cancer Detection for Patients Who Present with Hematuria: View
  • Cxbladder Monitor - Bladder Cancer Surveillance for Patients with Urothelial Carcinoma: View 

 UroToday Cxbladder Webinar

 

Greater Confidence in the Rule Out of Urothelial Cancer

Cxbladder is a reliable suite of tests for UC rule out that can help you make informed care decisions.

Contact Us to Request More Information

 

Last Updated: 21 Dec 2023 12:19 pm

  • References

    Pacific Edge is responsible for the development and determination of the performance characteristics for Cxbladder. Because Cxbladder is a Laboratory Developed Test (LDT), Cxbladder has not been cleared or approved by the US Food and Drug Administration (FDA).

Diagnosing bladder cancer

Drs Sia Daneshmand and Joseph DiTrolio discuss the guidelines, issues and technologies for diagnosing UC in patients presenting with hematuria in primary care.

Diagnosing bladder cancer
Diagnosing bladder cancer