Safety Analysis and Oncological Outcomes in HoLERT vs TURBT

Trial Title: Safety Analysis and Oncological Outcomes in HoLERT vs TURBT

NCT ID: NCT05833997

Condition: Bladder Urothelial Carcinoma
Bladder Cancer

Conditions: Official terms:
Urinary Bladder Neoplasms

Conditions: Keywords:
Bladder urothelial cancer
bladder cancer
transurethral resection of bladder tumor
En-bloc Resection of Bladder Tumors

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: Randomized

Intervention model: Crossover Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Procedure
Intervention name: Monopolar Transurethral resection of bladder tumor
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.
Arm group label: Control arm

Intervention type: Procedure
Intervention name: Holmium Laser resection of bladder tumor (HoLEBT)
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.
Arm group label: Holmium Laser En-bloc Resection of Bladder Tumors (HoLERBT) arm

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.

Criteria for 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.

Gender: All

Minimum age: 18 Years

Maximum age: 80 Years

Healthy volunteers: No

Locations:

Facility:
Name: Instituto do Cancer do Estado de São Paulo (ICESP)

Address:
City: São Paulo
Country: Brazil

Status: Recruiting

Contact:
Last name: Alexandre Iscaife, MD, PhD
Email: alexandre.iscaife@hc.fm.usp.br

Start date: December 10, 2020

Completion date: December 2025

Lead sponsor:
Agency: Instituto do Cancer do Estado de São Paulo
Agency class: Other

Source: Instituto do Cancer do Estado de São Paulo

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05833997