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临床试验/NCT07187635
NCT07187635招募中不适用

The Guiding Value of Urinary Tumor DNA Testing in Repeat Transurethral Resection of Non-Muscle-Invasive Bladder Cancer: An Open-Label, Randomized Controlled, Multi-Center Clinical Study (Truce-LB01)

Tianjin Medical University Second Hospital7 个研究点 分布在 1 个国家目标入组 196 人开始时间: 2025年9月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
196
试验地点
7
主要终点
Recurrence-free survival (RFS)

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Participants must meet all of the following criteria to be eligible for the study:
  • •Male or female, aged 18 years or older.
  • •Histologically confirmed non-muscle-invasive bladder tumor, with no evidence of muscle-invasive bladder cancer or metastatic disease.
  • •Histologically confirmed urothelial carcinoma of the bladder or bladder tumor with urothelial carcinoma as the predominant component (>50%).
  • •At least one of the following conditions:
  • •Incomplete initial transurethral resection of bladder tumor (TURBT) or suspected incomplete resection.
  • •Absence of detrusor muscle in the initial TURBT pathological specimen (except for low-grade Ta stage tumors or carcinoma in situ [CIS]).
  • •T1 stage tumor.
  • •Willingness to provide a 50 mL urine sample between 2-6 weeks after the initial TURBT and prior to re-TURBT.
  • •Willingness to provide tumor tissue samples for pathological examination.
  • •Willingness to undergo genetic testing required for the trial.

排除标准

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

研究组 & 干预措施

Standard re-TURBT

Active Comparator

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.

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

utDNA-guided management

Experimental

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.

干预措施: utDNA Testing (Urine Tumor DNA Detection) (Diagnostic Test)

结局指标

主要结局

Recurrence-free survival (RFS)

时间窗: Up to 24 months from randomization

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

次要结局

  • Patient-reported outcomes(Up to 24 months from randomization.)
  • Progression-free survival (PFS)(Up to 24 months from randomization)
  • Pathological outcomes of second transurethral resection (re-TURBT)(Perioperative (day of repeat TURBT))

研究者

发起方
Tianjin Medical University Second Hospital
申办方类型
Other
责任方
Sponsor

研究点 (7)

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