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Safety Analysis and Oncological Outcomes in HoLERT vs TURBT

Primary Purpose

Bladder Urothelial Carcinoma, Bladder Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Monopolar Transurethral resection of bladder tumor
Holmium Laser resection of bladder tumor (HoLEBT)
Sponsored by
Instituto do Cancer do Estado de São Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bladder Urothelial Carcinoma focused on measuring Bladder urothelial cancer, bladder cancer, transurethral resection of bladder tumor, En-bloc Resection of Bladder Tumors

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients aged between 18 and 80 years old; Presence of bladder tumor > 3cm without signals of MIBC or advanced disease (US, CT scan or MRI 3 months before surgery) Able to understand and willing to sign a written informed consent document Satisfactory clinical pre operatory conditions for surgery with regional or general anesthesia. Exclusion Criteria: Previous diagnosis of muscle-invasive bladder cancer; Tumor's Invasive aspect (T2 or more) on image (US, TC or RNM); Previous TURBT in the last 5 years; Urethral stenosis; Previous intra-vesical os systemic chemotherapy or radiotherapy; Previous treatment with intravesical BCG No clinical conditions for regional or general anesthesia; Any other significant disease or disorder which, in the opinion of the investigator may either put the participant at risk because of trial participation or may influence the trial result, or the participant's ability ti participate in the trial.

Sites / Locations

  • Instituto do Cancer do Estado de São Paulo (ICESP)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Holmium Laser En-bloc Resection of Bladder Tumors (HoLERBT) arm

Control arm

Arm Description

Patients randomized to HoLERBT group will have their tumor resected using the Megapulse 70w (Richard Wolf).

Patients randomized to control arm will undergo a monopolar transurethral resection of bladder tumor.

Outcomes

Primary Outcome Measures

Presence of Detrusor Muscle (DM) on histopathological analysis of morcellated tumor from HoLERBT and TRUBT
Evaluate the presence of muscle layer in the samples of tumor resection

Secondary Outcome Measures

Compare intraoperative an peri-operative complications
Evaluate intra and peri-operative complications (according to Clavien-Dindo scale) between the two groups
Clinical recurrence-free survival
Clinical recurrence-free survival at 3, 6, 9, 12, 15, 18 and 24 months follow-up (US, CT-scan, MRI, cystoscopy, TURBT)
Clinical progression-free survival
Clinical progression-free survival at 3, 6, 9, 12, 15, 18 and 24 months follow-up (US, CT-scan, MRI, TURBT)
Overall and cancer-specific survival
Overall and cancer-specific survival at 13, 6, 9, 12, 15, 18 and 24 months follow-up

Full Information

First Posted
April 5, 2023
Last Updated
April 18, 2023
Sponsor
Instituto do Cancer do Estado de São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT05833997
Brief Title
Safety Analysis and Oncological Outcomes in HoLERT vs TURBT
Official Title
Safety Analysis and Oncological Outcomes in Endoscopic Bladder Tumor Resection With Laser Holmium Compared With Transurethral Resection: a Prospective and Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 10, 2020 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto do Cancer do Estado de São Paulo

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
Bladder urothelial cancer is the second most common urologic tumor and represents a worldwide public health problem. Most cases are diagnosed as non-muscle invasive tumors, and can be treated with transurethral resection of bladder tumor (TURBT). However, the electrical energy-based TURBT fragments the tumor, burning it to its own muscular layer leading to artifacts that may spoil the histopathological analysis, resulting in understaging after the first TURBT ranging from 30-64%, depending on the presence of detrusor muscle. Modern laser technologies have been emerging as an alternative to classical TURB using en bloc tumor resection technique (ERBT). Therefore, the laser is applied on tumor's pedicle to resect the whole and intact tumor without fragmentation or fulguration as occurs in TURBT. The purpose of using laser if to improve the resection quality, decrease intra and perioperative complications, avoid re-TURBT and reduce recurrence rates at the resection site and in distant sites. Thus, the purpose of this study is to evaluate Laser Holmium use for large tumors resection (>3cm), reducing complications, costs, and the need for new approaches, and improving the muscle layers samples.
Detailed Description
This is a single-institution, randomized, single-blinded, prospective, controlled study, with 2 groups - 50 patients in Holmium Laser En-bloc Resection of Bladder Tumors (HoLERBT) arm and 50 patients in TURBT arm. All the patients will undergo a new procedure between 30-60 days after the first one (monopolar re-TURBT). The laser group will be operated by an experienced surgeon with more than 50 cases of prostate resection. The monopolar TURBT group will be operated by institutions´s surgeons assistants, urologists with more than 2 years of experience in the area and more than 50 surgeries performed. Pathological samples will be analyzed in the FMUSP Urology Laboratory by a pathologist with huge experience in analysis of bladder tumors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Urothelial Carcinoma, Bladder Cancer
Keywords
Bladder urothelial cancer, bladder cancer, transurethral resection of bladder tumor, En-bloc Resection of Bladder Tumors

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Holmium Laser En-bloc Resection of Bladder Tumors (HoLERBT) arm
Arm Type
Experimental
Arm Description
Patients randomized to HoLERBT group will have their tumor resected using the Megapulse 70w (Richard Wolf).
Arm Title
Control arm
Arm Type
Active Comparator
Arm Description
Patients randomized to control arm will undergo a monopolar transurethral resection of bladder tumor.
Intervention Type
Procedure
Intervention Name(s)
Monopolar Transurethral resection of bladder tumor
Intervention Description
Patients randomized to Monopolar TURBT will be operated using a 26F continuous-flow resectoscope sheaths and a single-pole working element to exclusive use of the resection. The power will be set to cut in 80w and 60w. The technique that will be performed will be the classic endoscopic resection from the top of the tumor until reaching the base, taking a sample from the base of the lesion (muscle layer). Fragments will be removed through an Ellik evacuator, and the solution used will be 3% glycine. After the procedure, the patient will will be catheterized with a silicon catheter number 22F with three ways and continuous irrigation. After 30-60 days of the first procedure, all patients diagnosed with a lamina propria invasion in the uro-pathology analysis (T1) will be submitted to a new monopolar TURBT.
Intervention Type
Procedure
Intervention Name(s)
Holmium Laser resection of bladder tumor (HoLEBT)
Intervention Description
It will be used a 24-26F continuous-flow resectoscope sheath with a specific working element to use with a 600µm fiber to Laser Holmium. Patients will be operated with the Megapulse 70w (Richard Wolf) and laser will be set to deliver the energy of 0,5J and 30-40Hz frequency, 15-20W of final energy. The solution used will be 0,9% saline solution. The resection will start from the base of the lesion, reaching the muscle layer to obtain a sample and resection of the whole tumor, without fragmentation. After this, the morcellation will be performed in the apex of tumor sparing the base with a long nephroscope, and the patient will will be catheterized with a silicon catheter number 22F with three ways and continuous irrigation. The morcellated product will be sent to the pathology lab for detailed analysis.
Primary Outcome Measure Information:
Title
Presence of Detrusor Muscle (DM) on histopathological analysis of morcellated tumor from HoLERBT and TRUBT
Description
Evaluate the presence of muscle layer in the samples of tumor resection
Time Frame
Up to 1 month after the first surgery
Secondary Outcome Measure Information:
Title
Compare intraoperative an peri-operative complications
Description
Evaluate intra and peri-operative complications (according to Clavien-Dindo scale) between the two groups
Time Frame
During surgery
Title
Clinical recurrence-free survival
Description
Clinical recurrence-free survival at 3, 6, 9, 12, 15, 18 and 24 months follow-up (US, CT-scan, MRI, cystoscopy, TURBT)
Time Frame
Until 2 years after surgery
Title
Clinical progression-free survival
Description
Clinical progression-free survival at 3, 6, 9, 12, 15, 18 and 24 months follow-up (US, CT-scan, MRI, TURBT)
Time Frame
Until 2 years of surgery
Title
Overall and cancer-specific survival
Description
Overall and cancer-specific survival at 13, 6, 9, 12, 15, 18 and 24 months follow-up
Time Frame
Until 2 years of surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged between 18 and 80 years old; Presence of bladder tumor > 3cm without signals of MIBC or advanced disease (US, CT scan or MRI 3 months before surgery) Able to understand and willing to sign a written informed consent document Satisfactory clinical pre operatory conditions for surgery with regional or general anesthesia. Exclusion Criteria: Previous diagnosis of muscle-invasive bladder cancer; Tumor's Invasive aspect (T2 or more) on image (US, TC or RNM); Previous TURBT in the last 5 years; Urethral stenosis; Previous intra-vesical os systemic chemotherapy or radiotherapy; Previous treatment with intravesical BCG No clinical conditions for regional or general anesthesia; Any other significant disease or disorder which, in the opinion of the investigator may either put the participant at risk because of trial participation or may influence the trial result, or the participant's ability ti participate in the trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alexandre Iscaife, MD, PhD
Phone
+5511976280082
Email
alexandre.iscaife@hc.fm.usp.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William Nahas, MD, PhD
Organizational Affiliation
Instituto do Cancer do Estado de São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto do Cancer do Estado de São Paulo (ICESP)
City
São Paulo
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alexandre Iscaife, MD, PhD
Email
alexandre.iscaife@hc.fm.usp.br

12. IPD Sharing Statement

Plan to Share IPD
No
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Safety Analysis and Oncological Outcomes in HoLERT vs TURBT

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