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NCT07625527RecruitingPhase 2

Is Prolonged Systemic Immunotherapy Necessary After Achieving Tumor-free Status in Patients With Extensive Transurethrally Unresectable Very-high-risk NMIBC?

Randomized Trial of Active Surveillance Versus Continued Systemic Immunotherapy After Achieving Tumor-Free Status in Extensive Transurethrally Unresectable Very-High-Risk NMIBC

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

Patients with extensive transurethrally unresectable very-high-risk non-muscle-invasive bladder cancer (NMIBC) may achieve a tumor-free status after systemic immunotherapy-based bladder-sparing treatment combined with transurethral resection of bladder tumor (TURBT). However, the optimal duration of systemic immunotherapy after achieving a tumor-free status remains uncertain. Prolonged treatment may increase toxicity, treatment burden, and cost, while some patients may maintain durable disease control without continued therapy. This randomized study aims to evaluate whether active surveillance after achieving tumor-free status is a feasible alternative to continued systemic immunotherapy in patients with extensive transurethrally unresectable very-high-risk NMIBC. Patients will initially receive systemic immunotherapy-based treatment followed by disease evaluation using cystoscopy with biopsy and/or TURBT, urine cytology, urinary tumor DNA (utDNA), and imaging assessments. Patients who achieve tumor-free status after treatment and complete resection of visible disease will be randomized to either active surveillance or continued systemic immunotherapy. The study will evaluate recurrence outcomes, bladder preservation, progression, safety, and patient management strategies following achievement of tumor-free status. The trial also aims to explore the role of urinary tumor DNA in identifying patients who may safely undergo treatment de-escalation and active surveillance.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
120 (estimated)
First submitted
21 May 2026
Start date
30 May 2026
Primary completion date
30 Mar 2029
Lead sponsor
Tianjin Medical University Second Hospital
NCT number
NCT07625527

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 120
  • From 30 May 2026 to the primary completion date, 30 Mar 2029
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has concurrent upper tract urothelial carcinoma.
  • Has received prior systemic immunotherapy for metastatic urothelial carcinoma.
  • Is receiving systemic immunosuppressive therapy.

Other illness

  • Has muscle-invasive bladder cancer (≥T2), locally advanced unresectable disease, nodal disease, or distant metastasis.
  • Has active autoimmune disease requiring systemic treatment.
  • Has uncontrolled infection requiring systemic therapy.
  • Has another active malignancy requiring systemic treatment.
  • Has known active hepatitis B, hepatitis C, human immunodeficiency virus infection, or active tuberculosis.
  • Has any medical or psychiatric condition that, in the investigator's judgment, would interfere with study participation or interpretation of results.

Other

  • Has persistent visible tumor, positive bladder pathology, positive urine cytology, or positive utDNA before randomization.
  • Has pregnancy or breastfeeding.

Who the study is looking for

  • Has histologically confirmed very-high-risk non-muscle-invasive urothelial carcinoma of the bladder.
  • Has transurethrally unresectable bladder tumor, defined as visually incomplete TURBT and/or extensive high-volume disease considered unsuitable for complete and oncologically adequate transurethral resection.
  • Has undergone cystoscopy and TURBT evaluation before study enrollment.
  • Has received systemic PD-1/PD-L1 inhibitor-based bladder-sparing therapy before randomization.
  • Has achieved tumor-free status before randomization, defined as:
    • No visible bladder tumor on cystoscopy;
    • Negative bladder biopsy and/or TURBT pathology;
    • Negative urine cytology;
    • Negative urinary tumor DNA (utDNA);
    • No radiographic evidence of progression or metastasis.
  • Has Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
  • Has adequate organ function.
  • Has provided written informed consent.
    • Cohort A Only
  • Achieved tumor-free status at the initial response evaluation after induction systemic therapy.
  • Maintained tumor-free status after additional systemic therapy before randomization.
    • Cohort B Only
  • Did not achieve tumor-free status at the initial response evaluation because of residual non-muscle-invasive disease.
  • Subsequently underwent complete TURBT/resection of residual disease followed by additional systemic therapy.
  • Achieved tumor-free status at the second response evaluation before randomization.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
General Hospital of Tianjin Medical University
Coordinator of this site? Confirm its status
TianjinChinaRecruiting
Tianjin Hospital
Coordinator of this site? Confirm its status
TianjinChinaRecruiting
The Second Hospital of Tianjin Medical University
Coordinator of this site? Confirm its status
TianjinChinaRecruiting
Xingtai People's Hospital
Coordinator of this site? Confirm its status
XingtaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.