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RecruitingNCT07187635Updated Aug 14, 2026

Guiding Value of Urinary Tumor DNA Testing in Repeat Transurethral Resection of Non-Muscle-Invasive Bladder Cancer

An interventional study of Second Transurethral Resection of Bladder Tumor (re-TURBT) and utDNA Testing (Urine Tumor DNA Detection) in Bladder Cancer, Liquid Biopsy and Repeat Transurethral Resection of Bladder Tumor, sponsored by Tianjin Medical University Second Hospital. Recruiting at 7 sites in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-14.

Sponsored by Tianjin Medical University Second Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2025; still recruiting 1 year later.
Phase
Not applicable
Study type
Interventional
Enrollment
196
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

Non-muscle-invasive bladder cancer (NMIBC) accounts for approximately 75% of newly diagnosed bladder cancers and is characterized by a high risk of recurrence and progression. Current guidelines recommend that patients with stage T1 NMIBC undergo a second transurethral resection of bladder tumor (re-TURBT) within 2-6 weeks after the initial surgery to remove residual tumor, confirm staging, and obtain additional pathological information. However, the benefits of routine re-TURBT for all high-risk patients remain controversial, as many patients may not have residual disease, while the procedure carries surgical and anesthetic risks, physical and psychological burden, and additional healthcare costs.

Urine tumor DNA (utDNA) refers to DNA fragments shed by tumor cells into urine. It can be detected using molecular assays with high sensitivity and specificity, offering a non-invasive method for bladder cancer diagnosis and surveillance. Previous studies have shown that positive utDNA results after initial TURBT may be associated with residual disease and higher recurrence risk.

This multicenter, randomized controlled trial aims to evaluate whether utDNA testing can accurately identify NMIBC patients who are most likely to benefit from re-TURBT, thereby guiding the decision to perform the procedure. The goal is to optimize patient selection for re-TURBT, reduce unnecessary surgeries, and improve patient quality of life while maintaining oncologic safety.

02

Conditions studied

  • Bladder Cancer
  • Liquid Biopsy
  • Repeat Transurethral Resection of Bladder Tumor

Keywords

  • bladder cancer
  • liquid biopsy
  • second transurethral resection of bladder tumor
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In context

Urinary Bladder Neoplasms

1,616 studies on the registry are indexed under Urinary Bladder Neoplasms; 421 are open to participants now.

This study's planned enrollment of 196 is above the median of 60 across 1,163 interventional studies indexed under Urinary Bladder Neoplasms.

Browse Urinary Bladder Neoplasms studies →

Lead sponsor

Tianjin Medical University Second Hospital is the lead sponsor of 57 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Participants must meet all of the following criteria to be eligible for the study:

  1. Male or female, aged 18 years or older.
  2. Histologically confirmed non-muscle-invasive bladder tumor, with no evidence of muscle-invasive bladder cancer or metastatic disease.
  3. Histologically confirmed urothelial carcinoma of the bladder or bladder tumor with urothelial carcinoma as the predominant component (>50%).
  4. At least one of the following conditions:

    1. Incomplete initial transurethral resection of bladder tumor (TURBT) or suspected incomplete resection.
    2. Absence of detrusor muscle in the initial TURBT pathological specimen (except for low-grade Ta stage tumors or carcinoma in situ [CIS]).
    3. T1 stage tumor.
  5. Willingness to provide a 50 mL urine sample between 2-6 weeks after the initial TURBT and prior to re-TURBT.
  6. Willingness to provide tumor tissue samples for pathological examination.
  7. Willingness to undergo genetic testing required for the trial.

Exclusion criteria

Exclusion Criteria:

  1. Contraindications to transurethral resection of bladder tumor (TURBT).
  2. Concurrent malignancy of the upper urinary tract (ureter or renal pelvis).
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
196 participants (estimated)

Study arms

  • Active comparator
    Standard re-TURBT

    Participants with NMIBC who have undergone initial TURBT will not receive utDNA testing and will undergo a second transurethral resection of bladder tumor (re-TURBT) within 2-6 weeks after the initial surgery, per guideline-based management.

    Procedure: Second Transurethral Resection of Bladder Tumor (re-TURBT)

  • Experimental
    utDNA-guided management

    Participants with NMIBC who have undergone initial TURBT will receive urine tumor DNA (utDNA) testing. If utDNA positive, they will undergo re-TURBT within 2-6 weeks after the initial surgery. If utDNA negative, re-TURBT will be omitted and patients will continue guideline-based adjuvant therapy/surveillance as per protocol.

    Diagnostic Test: utDNA Testing (Urine Tumor DNA Detection)

Interventions

  • ProcedureSecond Transurethral Resection of Bladder Tumor (re-TURBT)

    Participants with NMIBC who have undergone initial TURBT will not receive utDNA testing and will undergo a second transurethral resection of bladder tumor (re-TURBT) within 2-6 weeks after the initial surgery, in accordance with current clinical guidelines.

  • Diagnostic testutDNA Testing (Urine Tumor DNA Detection)

    Participants with NMIBC who have undergone initial TURBT will receive urine tumor DNA (utDNA) testing. If utDNA is positive, the patient will undergo a second transurethral resection of bladder tumor (re-TURBT) within 2-6 weeks after the initial surgery. If utDNA is negative, re-TURBT will be omitted and patients will proceed to guideline-based adjuvant therapy or surveillance.

06

What researchers measure

Primary outcomes

  1. Recurrence-free survival (RFS)

    Time from randomization to the first documented event of bladder tumor recurrence (any grade), upper tract urothelial recurrence.

    Time frame: Up to 24 months from randomization

Secondary outcomes

  1. Progression-free survival (PFS)

    Time from initial TURBT to disease progression (development of muscle-invasive bladder cancer, distant metastasis).

    Time frame: Up to 24 months from randomization

  2. Pathological outcomes of second transurethral resection (re-TURBT)

    Proportion of patients with residual tumor, upstaging (higher T category at re-TURBT), or concomitant CIS among those undergoing repeat TURBT.

    Time frame: Perioperative (day of repeat TURBT)

  3. Patient-reported outcomes

    Health outcomes directly reported by the patient without interpretation by clinicians or others. These measures capture patients' perceptions of symptoms, functional status, health-related quality of life (HRQoL), and treatment-related burden.

    Time frame: Up to 24 months from randomization.

Other outcomes

  1. Correlation Between utDNA Status and Clinical Outcomes

    Association of urine utDNA results with cystoscopy findings, imaging results, and re-TURBT pathology; evaluation of diagnostic performance (sensitivity, specificity, predictive values, AUC) and relation to recurrence/progression.

    Time frame: Up to 24 months from randomization

07

Study locations

7 of 7 sites recruiting
  • Nanchang Second People's Hospital
    Nanchang, Anhui, China
    Recruiting
  • Sun Yat-sen Memorial Hospital of Sun Yat-sen University
    Guangzhou, Guangdong, China
    Recruiting
  • Xingtai People's Hospital
    Xingtai, Hebei, China
    Recruiting
  • The Second Affiliated Hospital of Kunming Medical University
    Kunming, Yunnan, China
    Recruiting
  • Renji Hospital
    Shanghai, China
    Recruiting
  • The Second Hospital of Tianjin Medical University
    Tianjin, 300000, China
    Recruiting
  • General Hospital of Tianjin Medical University
    Tianjin, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Icf

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07187635
Lead sponsor
Tianjin Medical University Second Hospital
Responsible party
Sponsor
First posted
Sep 23, 2025
Start date
Sep 28, 2025
Primary completion
Oct 1, 2027 (estimated)
Completion
Nov 1, 2027 (estimated)
Last update
Aug 14, 2026

Study contacts

Hailong Hu, MD
Contact
huhailong@tmu.edu.cn
+8613662096232

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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