En Bloc Bladder Tumor Resection: Prospective Randomized Study

Sponsor
Fundacio Puigvert (Other)
Overall Status
Recruiting
CT.gov ID
NCT04712201
Collaborator
KARL STORZ Endoscopy-America, Inc. (Industry)
300
1
2
96
3.1

Study Details

Study Description

Brief Summary

INTRODUCTION Bladder tumor is the second most common neoplasm in the genitourinary tract. Most cases of ex novo diagnosis of bladder cancers are present as non-invasive muscle tumors, which are treatable through endourological procedures. The current standard is based on conventional transurethral resection of bladder tumor, although high rates of recurrence have been reported following resection of the primary tumor. Given the importance of a correct initial diagnosis in these cases, en bloc transurethral resection has developed over the past 2 decades. This technique was born, according to the literature, with 3 main objectives: to improve the quality of the surgical piece for its anatomopathological reading, reduce the rate of postoperative complications and reduce the rate of relapses in the surgical bed. This technique is used as a common practice of tumor resection in other centers and has been shown in multiple publications that it does not increase surgical risk or negatively affect cancer results.

OBJECTIVE The objective of our study is to compare feasibility, perioperative complication rate, accuracy of staging and recurrence/progression rates when performing en bloc resection by means of different energies: monopolar, bipolar and laser energy.

MATERIAL AND METHODS Between April 2018 and June 2021, a prospective randomized study will be conducted including patients undergoing a transurethral resection of initial or recurrent bladder tumor, either unifocal or multifocal. Patients with tumors less than 3 cm and with less than 3 tumors shall be included if multiple. Patients with more than 3 tumors or tumors over 3cm, those with evidence of invasive muscle tumor(cT2) or those with evidence of remote metastasis, whether lymphatic or organic, will be excluded.

Patients will be randomized into two groups:
  • Group 1 (test): en bloc resection (n-180). It will be divided into 3 subgroups according to the energy used (monopolar, bipolar, laser energy).

  • Group 2 (control): Conventional transurethral resection (n-120). It will be divided into 2 subgroups depending on the energy used (monopolar or bipolar).

A fact sheet will be given to the patient about the study and the signature of the informed consent will be requested in order to be included. The patient will be free to leave the study at any time without having to provide any justification and without affecting the treatment, intervention and follow-up that must be carried out.

The processing and storage of samples will be carried out in the pathological anatomy laboratory, according to standard clinical practice.

Patients will be monitored according to the usual clinical practice protocol (minimum 5-year follow-up), included in the non-muscle invasive bladder tumor protocols of the Puigvert Foundation.

Condition or Disease Intervention/Treatment Phase
  • Procedure: En bloc transurethral resection of bladder tumor (TURBT)
  • Procedure: Conventional TURBT
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
En Bloc Bladder Tumor Resection: Prospective Randomized Evaluation of Monopolar, Bipolar and Laser Energy
Actual Study Start Date :
Apr 1, 2018
Anticipated Primary Completion Date :
Jun 1, 2021
Anticipated Study Completion Date :
Apr 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: En bloc

En bloc transurethral resection of the bladder

Procedure: En bloc transurethral resection of bladder tumor (TURBT)
En bloc transurethral resection of bladder tumor using thulium:yttrium aluminium garnet, monopolar and bipolar energy

Active Comparator: Conventional

Conventional transurethral resection of the bladder

Procedure: Conventional TURBT
Conventional transurethral resection of bladder tumor using monopolar and bipolar energy

Outcome Measures

Primary Outcome Measures

  1. Staging of bladder tumor [Three years]

    Evaluation of muscle presence in the specimen

Secondary Outcome Measures

  1. Intraoperative complications [Three years]

    Bladder perforation grading, obturatory reflex, conversions to conventional TURB

  2. Rate of planned adjuvant treatment [Three years]

    Rate of planned postoperative single instillation of mitomycin/epirubicin

  3. Post-operative complications [Three years]

    Post-operative complications according to Clavien-Dindo System

  4. Substaging T1 bladder cancer [Three years]

    T1a, T1b and T1c

  5. Recurrence-free survival [Through study completion, an average of five years]

    Recurrence of bladder cancer

  6. Progression-free survival [Through study completion, an average of five years]

    Progression of bladder cancer

  7. Disease-free survival [Through study completion, an average of five years]

    Disease-free survival

  8. Cancer specific survival [Through study completion, an average of five years]

    Cancer specific survival

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Unifocal primary or recurrent bladder cancer with size less or equal than 3 cm

  • Multifocal primary or recurrent bladder cancer less or equal than 3 lesions and with size less or equal than 3 cm

Exclusion Criteria:
  • Evidence of > 3 tumors or > 3 cm

  • Computed tomography/cystoscopy suspect of muscle-invasive bladder cancer (cT2 or higher)

  • Computed tomography/magnetic resonance evidence of distant metastases

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fundacio Puigvert Barcelona Spain 08025

Sponsors and Collaborators

  • Fundacio Puigvert
  • KARL STORZ Endoscopy-America, Inc.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Alberto Breda, Chief of the Uro-Oncology Division and Kidney Transplant Unit, Fundacio Puigvert
ClinicalTrials.gov Identifier:
NCT04712201
Other Study ID Numbers:
  • 2017/09c
First Posted:
Jan 15, 2021
Last Update Posted:
Jan 15, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Alberto Breda, Chief of the Uro-Oncology Division and Kidney Transplant Unit, Fundacio Puigvert
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 15, 2021