Transurethral En Bloc Versus Standard Resection of Bladder Tumour
Primary Purpose
Bladder Cancer
Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Bipolar transurethral standard resection
Bipolar transurethral en bloc resection
Sponsored by
About this trial
This is an interventional treatment trial for Bladder Cancer focused on measuring Bladder cancer, Transurethral resection, En bloc resection, TURBT
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years old with informed consent
Exclusion Criteria:
- Bladder tumour base with maximal dimension of >3cm (Anticipated difficulty in retrieving the specimen en bloc)
- Bladder tumour detected during intravesical BCG therapy (BCG failure warrants more aggressive treatment, i.e. radical cystectomy)
- Histological diagnosis other than NMIBC
- Presence or prior history of upper urinary tract malignancy
- ECOG performance status ≥ 3 (Confined to bed or chair more than 50% of waking hours)
- ASA III or above (Patient with severe systemic disease)
- History of bleeding disorder or use of anti-coagulants
- Pregnancy
- Presence of other active malignancy
- Life expectancy of less than one year
Sites / Locations
- Caritas Medical Centre
- Kwong Wah Hospital
- North District Hospital
- Our Lady of Maryknoll Hospital
- Pok Oi Hospital
- Prince of Wales Hospital
- Princess Margaret Hospital
- Queen Elizabeth Hospital
- Queen Mary Hospital
- Tseung Kwan O Hospital
- Tuen Mun Hospital
- Tung Wah Hospital
- United Christian Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Standard resection
En bloc resection
Arm Description
For patients undergoing bipolar transurethral standard resection, bladder tumour is resected in a piecemeal manner.
For patients undergoing bipolar transurethral en bloc resection, bladder tumour is resected and removed in one piece.
Outcomes
Primary Outcome Measures
One-year recurrence rate
Rate of disease recurrence one year after the operation
Secondary Outcome Measures
Detrusor muscle sampling rate
Rate of presence of detrusor muscle in the pathological specimen
Occurrence of obturator reflex
Number of participants with obturator reflex encountered by the operating surgeon during the operation
Operative time
Duration of operation
Rate of mitomycin C instillation
Rate of mitomycin C instillation given after the operation
Hospital stay
Patients undergoing transurethral resection surgery have an average hospital stay of three days.
30-day complications
Complications which occur within 30 days after the operation
Residual disease upon second look transurethral resection surgery
Second look transurethral resection surgery is expected to perform within six weeks after the allocated treatment and one more week is allowed for histological assessment of the second look transurethral resection specimen. Residual disease is measured by the number of participants with the presence of urothelial carcinoma in the second look transurethral resection specimen.
Upstaging of disease upon second look transurethral resection surgery
Second look transurethral resection surgery is expected to perform within six weeks after the allocated treatment and one more week is allowed for histological assessment of the second look transurethral resection specimen. Upstaging of disease is measured by the number of participants with upstaging of disease from non-muscle-invasive bladder cancer to muscle-invasive bladder cancer in the second look transurethral resection specimen.
One-year progression rate
Rate of disease progression one year after the operation
Full Information
NCT ID
NCT02993211
First Posted
December 8, 2016
Last Updated
June 24, 2022
Sponsor
Chinese University of Hong Kong
Collaborators
Kwong Wah Hospital, North District Hospital, Our Lady of Maryknoll Hospital, Pok Oi Hospital, The University of Hong Kong, Tseung Kwan O Hospital, Hong Kong, Tuen Mun Hospital, Tung Wah Hospital, United Christian Hospital, Princess Margaret Hospital, Hong Kong, Caritas Medical Centre, Hong Kong, Queen Elizabeth Hospital, Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT02993211
Brief Title
Transurethral En Bloc Versus Standard Resection of Bladder Tumour
Official Title
Transurethral En Bloc Versus Standard Resection of Bladder Tumour: A Multi-centre Randomised Controlled Trial (EB-StaR Study).
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
April 18, 2017 (Actual)
Primary Completion Date
February 11, 2022 (Actual)
Study Completion Date
June 9, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
Collaborators
Kwong Wah Hospital, North District Hospital, Our Lady of Maryknoll Hospital, Pok Oi Hospital, The University of Hong Kong, Tseung Kwan O Hospital, Hong Kong, Tuen Mun Hospital, Tung Wah Hospital, United Christian Hospital, Princess Margaret Hospital, Hong Kong, Caritas Medical Centre, Hong Kong, Queen Elizabeth Hospital, Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Conventionally, transurethral standard resection (SR) of bladder tumour is performed in a piecemeal manner. Transurethral en bloc resection (EBR) has been described as an alternate surgical technique in bladder tumour resection. By preventing tumour fragmentation and ascertaining complete tumour resection by histological assessment of the EBR specimen, we hypothesized that EBR could reduce disease recurrence as compared to SR.
Detailed Description
Bladder cancer is the 9th most commonly diagnosed cancer in men worldwide, with a standardized incidence rate of 9.0 per 100,000 person-years for men and 2.2 per 100,000 person-years for women. In Hong Kong, more than 400 new cases of bladder cancer are diagnosed every year. It is a common and important disease which carries a significant burden to the health medical system.
For patients who are diagnosed to have bladder tumours upon flexible cystoscopy, transurethral resection of bladder tumour (TURBT) should be offered. Being a minimally invasive procedure, it has become the standard for the initial management of bladder cancer. This operation aims to ascertain the diagnosis, to correctly stage the tumour (T-stage) and to cure the disease in the case of non-muscle-invasive bladder cancer (NMIBC). However, in a combined analysis of 2,596 patents from 7 randomised controlled trials in patients with NMIBC, it was shown that 1-year recurrence rate ranged from 15-61%, and 5-year recurrence rate ranged from 31-78%. Despite possible complete tumour resection during TURBT, the oncological control of NMIBC is far from satisfactory.
There are two main problems with the conventional standard resection (SR) procedure. First, the bladder tumour is resected in a piecemeal manner. This results in tumour fragmentation and floating tumour cells inside the bladder. The tumour cells may re-implant on to the bladder wall and lead to early disease recurrence. Second, 'complete tumour resection' is often determined by endoscopic vision only. Due to the inherited nature of piecemeal resection, it is not possible to assess the resection margin by histological means. The charring effect to the resection bed may also hinder the judgement of a 'complete tumour resection'. Routine second-look TURBT has been advocated for selected patients (Any presence of T1 disease, G3 disease, or any absence of detrusor muscle in the first TURBT specimen) even after a 'complete tumour resection' during the first TURBT. Second-look TURBT has been shown to detect residual disease in 33-55% of the patients and upstaging of disease in 4-45% of the patients. These results highlighted the limitations of TURBT in ascertaining complete tumour resection.
Transurethral en bloc resection (EBR) has been described as an alternate surgical technique in bladder tumour resection. By preventing tumour fragmentation and ascertaining complete tumour resection by histological assessment of the EBR specimen, we hypothesized that EBR could reduce disease recurrence as compared to SR.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer
Keywords
Bladder cancer, Transurethral resection, En bloc resection, TURBT
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
350 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard resection
Arm Type
Active Comparator
Arm Description
For patients undergoing bipolar transurethral standard resection, bladder tumour is resected in a piecemeal manner.
Arm Title
En bloc resection
Arm Type
Experimental
Arm Description
For patients undergoing bipolar transurethral en bloc resection, bladder tumour is resected and removed in one piece.
Intervention Type
Device
Intervention Name(s)
Bipolar transurethral standard resection
Intervention Description
Olympus TURis Bipolar HF-resection electrode (Model: WA22306D)
Intervention Type
Device
Intervention Name(s)
Bipolar transurethral en bloc resection
Intervention Description
Olympus TURis Bipolar HF-resection electrode (Model: WA22306D)
Primary Outcome Measure Information:
Title
One-year recurrence rate
Description
Rate of disease recurrence one year after the operation
Time Frame
One year after the allocated treatment
Secondary Outcome Measure Information:
Title
Detrusor muscle sampling rate
Description
Rate of presence of detrusor muscle in the pathological specimen
Time Frame
One week after the allocated treatment
Title
Occurrence of obturator reflex
Description
Number of participants with obturator reflex encountered by the operating surgeon during the operation
Time Frame
Intra-operative
Title
Operative time
Description
Duration of operation
Time Frame
Immediately post-operative
Title
Rate of mitomycin C instillation
Description
Rate of mitomycin C instillation given after the operation
Time Frame
One day after the allocated treatment
Title
Hospital stay
Description
Patients undergoing transurethral resection surgery have an average hospital stay of three days.
Time Frame
Three days after the allocated treatment
Title
30-day complications
Description
Complications which occur within 30 days after the operation
Time Frame
Thirty days after the allocated treatment
Title
Residual disease upon second look transurethral resection surgery
Description
Second look transurethral resection surgery is expected to perform within six weeks after the allocated treatment and one more week is allowed for histological assessment of the second look transurethral resection specimen. Residual disease is measured by the number of participants with the presence of urothelial carcinoma in the second look transurethral resection specimen.
Time Frame
Seven weeks after the allocated treatment
Title
Upstaging of disease upon second look transurethral resection surgery
Description
Second look transurethral resection surgery is expected to perform within six weeks after the allocated treatment and one more week is allowed for histological assessment of the second look transurethral resection specimen. Upstaging of disease is measured by the number of participants with upstaging of disease from non-muscle-invasive bladder cancer to muscle-invasive bladder cancer in the second look transurethral resection specimen.
Time Frame
Seven weeks after the allocated treatment
Title
One-year progression rate
Description
Rate of disease progression one year after the operation
Time Frame
One year after the allocated treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years old with informed consent
Exclusion Criteria:
Bladder tumour base with maximal dimension of >3cm (Anticipated difficulty in retrieving the specimen en bloc)
Bladder tumour detected during intravesical BCG therapy (BCG failure warrants more aggressive treatment, i.e. radical cystectomy)
Histological diagnosis other than NMIBC
Presence or prior history of upper urinary tract malignancy
ECOG performance status ≥ 3 (Confined to bed or chair more than 50% of waking hours)
ASA III or above (Patient with severe systemic disease)
History of bleeding disorder or use of anti-coagulants
Pregnancy
Presence of other active malignancy
Life expectancy of less than one year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeremy YC Teoh, MBBS
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Caritas Medical Centre
City
Hong Kong
Country
Hong Kong
Facility Name
Kwong Wah Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
North District Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Our Lady of Maryknoll Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Pok Oi Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Prince of Wales Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Princess Margaret Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Queen Elizabeth Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Queen Mary Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Tseung Kwan O Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Tuen Mun Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Tung Wah Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
United Christian Hospital
City
Hong Kong
Country
Hong Kong
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
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16442208
Citation
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Results Reference
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Citation
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Citation
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Citation
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Transurethral En Bloc Versus Standard Resection of Bladder Tumour
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