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En-Bloc Resection of Bladder Tumors

Primary Purpose

Bladder Neoplasm

Status
Recruiting
Phase
Phase 2
Locations
Turkey
Study Type
Interventional
Intervention
En Bloc Resection
Conventional Transurethral Resection Bladder Tumor (Mono/Bipolar)
Sponsored by
Betul Kartal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Bladder Neoplasm focused on measuring Urinary Bladder Neoplasms, Urologic Neoplasms, Urogenital Neoplasms

Eligibility Criteria

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

Inclusion Criteria:

  • Age: 18 years old and older (adult, older adult) Sexes: All Accepts healthy volunteers: No

Inclusion criteria:

  • Patients aged 18 and older presenting with suspicion of primary or recurrent Non-muscle invasive bladder cancer (NMIBC)
  • Tumor size estimated by cystoscopy ≤ 3 cm
  • Solitary or multiple tumors (up to 3 in number)

Exclusion Criteria:

  • Tumor size > 3 cm of maximum dimeter
  • Patient with severe systemic disease (ASA III+)
  • Location on the anterior bladder wall and/ or anterior bladder neck (relative contraindication depending on accessibility)
  • Pregnancy
  • Histological diagnosis other than NMIBC urothelial bladder cancer
  • Presence or history of previous upper-tract urinary cancer (UTUC)
  • Presence of positive cytology without macroscopic identifiable bladder tumor
  • Life expectancy < 1 year
  • Non-reversible coagulopathy
  • Bladder tumor detected during intravesical BCG therapy
  • Tumor multiplicity (> 3 tumors)

Contacts and locations:

Sites / Locations

  • Bagcilar Education and Research HospitalRecruiting
  • Medipol Mega University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

En Bloc Resection Bladder Tumor (Any energy source)

Conventional Transurethral Resection Bladder Tumor (Mono/Bipolar)

Arm Description

Patients with suspicion of NMIBC (primary or recurrent) that underwent en bloc resection (EBRT

Patients with suspicion of NMIBC (primary or recurrent) that underwent conventional TURBT

Outcomes

Primary Outcome Measures

Pathological Staging
Staging of NMIBC is defined by the presence of sufficient detrusor in the EBR-BT specimens, the status of the margins, presence of a tumor and /or CIS in the mucosal margins, the status of the detrusor margin, and suspicion of instability in mucosa free of tumor.
Recurrence at 3 months
Recurrence free survival at 3-months (absence of visible tumors at the site of the previous resection

Secondary Outcome Measures

Operative Complications
Rate of operative complications (estimated bleeding, bladder perforation, obturatory reflex, tumor fragmentation, conversion to conventional TURBT)
Perioperative Complications
Postoperative complications according to Clavien-Dindo classification

Full Information

First Posted
February 26, 2021
Last Updated
April 11, 2022
Sponsor
Betul Kartal
Collaborators
Bağcılar Eğitim ve Araştırma Hastanesi
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1. Study Identification

Unique Protocol Identification Number
NCT04784507
Brief Title
En-Bloc Resection of Bladder Tumors
Official Title
En-Bloc Resection of Bladder Tumors: a Multicentric Safety and Feasibility Trial (IDEAL Phase II) vs Conventional Resection of Bladder Tumors?
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2020 (Actual)
Primary Completion Date
May 31, 2022 (Anticipated)
Study Completion Date
July 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Betul Kartal
Collaborators
Bağcılar Eğitim ve Araştırma Hastanesi

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
Observational data shows that "en bloc" resection of bladder tumor (EBR-BT) may entail advantages when compared with conventional transurethral bladder tumor resection (TURBT). EBR-BT has the potential to increase the rate of correct staging and accurate assignment of risk-classification in non-muscle-invasive bladder cancer (NMIBC) and to avoid re-TURBT in a considerable number of high-grade NMIBC by demonstrating total macro and microscopic eradication of the primary tumor and to provide the basis for a correct treatment based on a correct stage. Following the rules of the IDEAL collaboration evaluation and stages of surgical innovation and considering EBR-BT as a surgical technical innovation, the investigators designed a multi-institutional, stage 2a/b study on feasibility (procedural success), safety (including pathology features), and short-term efficacy of EBR-BT and as proof of concept on the reliability of NMIBC staging. Main objective: to prospectively assess the pathological efficacy of EBR-BT in the staging of bladder cancer and the clinical efficacy at short-term recurrence-free survival. Secondary objectives: To assess the clinical efficacy at short-term (3-months) of EBR-BT, and to compare efficacy in the staging of the EBR-BT with the conventional TURBT.
Detailed Description
En-bloc resection of bladder tumors (EBR-BT) has been showing certain advantages over conventional transurethral resection technique (TURBT) in non-muscle-invasive bladder cancer. These advantages consist mainly in the reduction of obturator nerve reflex and obtention of surgical samples according to oncological principles. Advantages in terms of tumor recurrence in the short-term, when compared with TURBT, remain uncertain. Herein several randomized control trials aim to assess comparative outcomes in the short and long term. A higher rate of detrusor muscle is found in the EBR-BT samples than in the conventional samples resulting in a better staging and at least theoretically the need for fewer re-TURBT indications. However, a detailed and scrupulous description of the histopathological samples is lacking and, it is assumed that the presence of detrusor in the sample without solution of continuity with submucosa and tumor is sufficient to stage. As in surgical samples of other organs, the objective of EBR-RT is not only to obtain detrusor, but also clean margins that ensure the radicality of the tumor. The hypothesis of the investigators' is that EBR-BT will results in an increased rate of pathological specimen with the presence of detrusor muscle and free-tumor margins, hence a more accurate stage than TURBT and a decrease in 3-months recurrence at short-term (3 months)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Neoplasm
Keywords
Urinary Bladder Neoplasms, Urologic Neoplasms, Urogenital Neoplasms

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
En Bloc Resection Bladder Tumor (Any energy source)
Arm Type
Experimental
Arm Description
Patients with suspicion of NMIBC (primary or recurrent) that underwent en bloc resection (EBRT
Arm Title
Conventional Transurethral Resection Bladder Tumor (Mono/Bipolar)
Arm Type
Active Comparator
Arm Description
Patients with suspicion of NMIBC (primary or recurrent) that underwent conventional TURBT
Intervention Type
Procedure
Intervention Name(s)
En Bloc Resection
Intervention Description
En bloc transurethral resection of bladder tumor (EBR-BT) using any energy source (laser and bipolar or monopolar energy)
Intervention Type
Procedure
Intervention Name(s)
Conventional Transurethral Resection Bladder Tumor (Mono/Bipolar)
Intervention Description
Conventional Transurethral Resection Bladder Tumor (Mono/Bipolar)
Primary Outcome Measure Information:
Title
Pathological Staging
Description
Staging of NMIBC is defined by the presence of sufficient detrusor in the EBR-BT specimens, the status of the margins, presence of a tumor and /or CIS in the mucosal margins, the status of the detrusor margin, and suspicion of instability in mucosa free of tumor.
Time Frame
Immediately after the intervention
Title
Recurrence at 3 months
Description
Recurrence free survival at 3-months (absence of visible tumors at the site of the previous resection
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Operative Complications
Description
Rate of operative complications (estimated bleeding, bladder perforation, obturatory reflex, tumor fragmentation, conversion to conventional TURBT)
Time Frame
intraoperative
Title
Perioperative Complications
Description
Postoperative complications according to Clavien-Dindo classification
Time Frame
Up to 90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 18 years old and older (adult, older adult) Sexes: All Accepts healthy volunteers: No Inclusion criteria: Patients aged 18 and older presenting with suspicion of primary or recurrent Non-muscle invasive bladder cancer (NMIBC) Tumor size estimated by cystoscopy ≤ 3 cm Solitary or multiple tumors (up to 3 in number) Exclusion Criteria: Tumor size > 3 cm of maximum dimeter Patient with severe systemic disease (ASA III+) Location on the anterior bladder wall and/ or anterior bladder neck (relative contraindication depending on accessibility) Pregnancy Histological diagnosis other than NMIBC urothelial bladder cancer Presence or history of previous upper-tract urinary cancer (UTUC) Presence of positive cytology without macroscopic identifiable bladder tumor Life expectancy < 1 year Non-reversible coagulopathy Bladder tumor detected during intravesical BCG therapy Tumor multiplicity (> 3 tumors) Contacts and locations:
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rahim Horuz
Phone
+90533 934 38 50
Email
rhoruz@medipol.edu.tr
First Name & Middle Initial & Last Name or Official Title & Degree
Betul Kartal
Email
bbkartal@medipol.edu.tr
Facility Information:
Facility Name
Bagcilar Education and Research Hospital
City
Istanbul
State/Province
Bagcilar
ZIP/Postal Code
34200
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bagcilar
Phone
(0212) 440 40 00
Facility Name
Medipol Mega University Hospital
City
Istanbul
State/Province
Bagcilar
ZIP/Postal Code
34214
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Medipol
Phone
444 7 044

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Data will be provided by request according to the primary objectives of the IPD study and according to the availability in the present trial

Learn more about this trial

En-Bloc Resection of Bladder Tumors

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