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临床试验/NCT07724886
NCT07724886尚未招募不适用

A Randomised Trial Investigating the Role of Transurethral En Bloc Resection of Bladder Tumour Plus Intravesical Bacillus Calmette-Guerin Therapy, in Patients With Intermediate-Risk or High-Risk Non-Muscle-Invasive Bladder Cancer

Chinese University of Hong Kong2 个研究点 分布在 1 个国家目标入组 732 人开始时间: 2026年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
732
试验地点
2
主要终点
Rate of recurrence-free survival

研究概览

简要总结

This is a prospective, multi-centre randomised trial comparing between cTURBT plus 1-year BCG therapy, and ERBT plus 1-year BCG therapy, in patients with intermediate-risk or high-risk NMIBC.

详细描述

All patients who are diagnosed to have bladder tumour(s) upon flexible cystoscopy will be screened for study eligibility. Imaging will be arranged to rule out any upper urinary tract malignancy. Patients are randomised to receive either transurethral ERBT or cTURBT with an allocation ratio of 1:1. A single dose of intravesical mitomycin C will be instilled according to the EAU guidelines, i.e. in all patients except those with a prior recurrence rate of more than one recurrence per year, or those with an EORTC recurrence score of ≥5. All patients will be followed up at our outpatient clinic and the pathology results will be reviewed. Routine second-look TURBT will be arranged within 2-6 weeks after the first operation should there be any indications as stated in the EAU guidelines. For patients in the intermediate or high-risk groups, 1-year of intravesical BCG therapy will be offered. Surveillance flexible cystoscopy will be performed at a 3-month interval until 2 years after the index surgery, and then every 6 months for another 3 years. Biopsy will be taken and TURBT will be offered if there is any suspicious tumour recurrence noted during surveillance cystoscopy.Primary outcome is recurrence-free survival at 2 years.

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

入选标准

  • Age 18 years or above
  • Fulfil any one of the following three criteria:
  • Recurrent bladder tumour
  • Multiple bladder tumours
  • Any bladder tumour size of >1cm

排除标准

  • EAU low-risk NIMBC as intravesical BCG therapy should not be offered (5)
  • EAU very high-risk NMIBC as upfront radical cystectomy should be offered (5)
  • Any prior use of intravesical BCG therapy
  • Presence or prior history of upper urinary tract malignancy
  • Presence of clinically significant cardiovascular disease (History of acute myocardial infarction, presence of uncontrolled angina within 3 months before screening, New York Heart Association Class III or IV congestive heart failure, presence of ventricular arrhythmias, or presence of second-degree or third-degree heart block) (16)
  • Presence of GOLD Stage III or IV chronic obstructive pulmonary disease
  • ECOG performance status ≥ 2 (Ambulatory and capable of all self-care but unable to carry our any work activities) (18)
  • History of bleeding disorder or use of anti-coagulants
  • Pregnancy
  • Presence of other active malignancy

研究组 & 干预措施

Transurethral En Bloc Resection of Bladder Tumour (ERBT)

Experimental

干预措施: Transurethral En Bloc Resection of Bladder Tumour (Procedure)

Conventional Transurethral Resection of Bladder Tumour (cTURBT)

Active Comparator

干预措施: Conventional Transurethral Resection of Bladder Tumour (Procedure)

结局指标

主要结局

Rate of recurrence-free survival

时间窗: At Year 2

次要结局

  • Detrusor muscle sampling rate(On Day 30 after operation)
  • Day of hospital stay(On Day 30 after operation)
  • Total operation time(On Day 30 after operation)
  • Overall survival(At Year 2)
  • Rate of progression-free survival(At Year 2)
  • Cancer-specific survival(At Year 2)
  • Adverse Events(On Day 30 after operation)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jeremy Yuen Chun TEOH

Associate Professor

Chinese University of Hong Kong

研究点 (2)

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