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Cancer Screening

Cxbladder® Detect

Risk stratification for microhaematuria — reduce unnecessary cystoscopy

Turnaround Time2 working weeks
🧪Specimen TypeUrine
🔬MethodRT-PCR gene expression analysis (5-gene mRNA panel)
AccreditationsCLIA-certified
Cxbladder® Detect

Cxbladder® Detect is a urine genomic test designed to improve workflow efficiency in urological care. It is optimised for patients presenting with microhaematuria and helps to de-intensify the clinical work-up in those with a low-probability result. It also resolves atypical urine cytology and equivocal cystoscopy findings.

Patients with microhaematuria where risk stratification is needed before or after cystoscopy. Resolves equivocal cystoscopy and atypical cytology results as a reliable adjunct test.

⚠ Not intended for:

Not for active urinary tract infection. Not a standalone replacement for cystoscopy in high-risk patients.

CDC2IGFBP5HOXA13MDKCXCR2
Step / TestAccuracyNotes
Sensitivity82%
Specificity94%
Specimen Type: Urine
Preferred Collection:

Urine in Cxbladder container

30–50 mL midstream urine collected into the Cxbladder collection tube (contains preservative). Do not use catheter samples.

Rejection Criteria:
  • First void urine (Only 2nd pass of the day or later is accepted)
  • Grossly bloody urine
  • Acute UTI (Treat UTI first and delay test for 2 weeks)
  • <2 weeks after cystoscopy
  • <6 weeks after BCG

Available through Codex Genetics as the authorised Pacific Edge distributor in Hong Kong.

Shipping Instructions:

Cxbladder specimens must be collected using the dedicated Cxbladder collection kit.

  1. Request a collection kit from your healthcare provider or Codex Genetics.
  2. Collect midstream urine (30–50 mL) into the provided tube with preservative.
  3. Seal securely; store at room temperature.
  4. Deliver to Codex Genetics Laboratory within 5 days of collection. Address: Unit 220, 2/F, Building 16W, HKSTP, Pak Shek Kok, NT, Hong Kong.

Please contact us for pricing.

  1. Low/Negligible Risk Patients:
    • Clinicians should obtain repeat urinalysis within six months rather than perform immediate cystoscopy or imaging
  2. Intermediate Risk Patients:
    • Clinicians should recommend cystoscopy and renal ultrasound
    • Clinicians may offer urine cytology or validated urine-based tumor markers to appropriately counseled patients to facilitate the decision regarding utility of cystoscopy; renal and bladder ultrasound should still be performed.
    • If UBTM used to defer cystoscopy, repeat urinalysis within 1 year. Patients with persistent microhematuria should undergo cystoscopy
  3. High Risk Patients:
    • Clinicians should perform cystoscopy and axial upper tract imaging

Microhaematuria is common in the general population and drives high cystoscopy volumes. The majority of microhaematuria cases are benign. Cxbladder Detect enables clinicians to identify low-risk patients who may not need invasive investigation, reducing patient anxiety and healthcare costs while maintaining safety.