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Intravesically Heated Thermo-chemotherapy With Mitomycin-C Prior to TURBT

Primary Purpose

Transitional Cell Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
BWT with Mitomycin-C prior TURBT
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Transitional Cell Carcinoma focused on measuring Recurrence

Eligibility Criteria

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

Inclusion Criteria:

  1. Adult patients (>18 yrs.) with good performance status according to Eastern Cooperative Oncology Group (ECOG) scale, designed to TURBT and gave their consent to participate in our research.
  2. All participants must have adequate blood tests (CBC, Creatinine, electrolytes and liver function tests).

Exclusion Criteria:

  1. Concurrent other malignancy in the urinary system (e.g. upper tract UC)
  2. Urothelial malignancy of the bladder other then carcinoma
  3. Diffuse carcinoma in situ on preliminary cystoscopy
  4. Allergy or sensitivity to MMC
  5. Known urinary bladder capacity of less then 200cc
  6. Concurrent complicated urinary infection
  7. Autoimmune disease or patient under immunosuppressive therapy
  8. presence of urethral stricture
  9. Previous pelvic radiotherapy
  10. Concomitant malignancy of other organ
  11. Pregnancy
  12. Children under 18 years.

Sites / Locations

  • Sheba Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

TURBT ONLY

BWT with Mitomycin-C prior TURBT

Arm Description

A total of 150 patients in this arm will be divided into five follow-up sub groups according to pathology reports. Group 1 - Primary Low risk patients Group 2 - Primary Intermediate risk patients Group 3 - Primary High risk patients Group 4 - Recurrent Intermediate risk patients Group 5 - Recurrent Intermediate risk patients

A total of 150 patients in this arm will be divided into five follow-up sub groups according to pathology reports. Group 1 - Primary Low risk patients Group 2 - Primary Intermediate risk patients Group 3 - Primary High risk patients Group 4 - Recurrent Intermediate risk patients Group 5 - Recurrent Intermediate risk patients

Outcomes

Primary Outcome Measures

Recurrence rate of Urothelial carcinoma (UC) of bladder
Reduced recurrence rate of Urothelial carcinoma (UC) of bladder among patients receiving intravesical heated installations

Secondary Outcome Measures

Full Information

First Posted
May 27, 2015
Last Updated
April 27, 2016
Sponsor
Sheba Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02471547
Brief Title
Intravesically Heated Thermo-chemotherapy With Mitomycin-C Prior to TURBT
Official Title
Intravesically Heated Thermo-chemotherapy With Mitomycin-C Prior to TURBT- Prospective Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
January 2018 (Anticipated)
Study Completion Date
January 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sheba Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Transurethral Resection of Bladder Tumor (TURBT) is the initial treatment procedure for urinary bladder cancer. Recurrence rate during the first year ranges between 15-38% in case of low-intermediate disease. Current literature advocate using intravesical instillations of Mitomycin-C (MMC) immediately post TURBT in order to reduce the rate of recurrence. During the last decade, heated intravesical instillations have emerged as additional players, in the treatment of recurrent disease. By most cases, the heated intravesical instillations are given either by microwave hyperthermia (synergo®) or by conductive heat bladder wall thermo-chemotherapy (BWT). Previous reports suggest up to 59% reduction rate in recurrence following thermo-chemotherapy upon recurrent disease. These outstanding reduction results haven't convinced significant amount of urologists worldwide to use the intravesical instillation close after endoscopic resection as TURBT, probably due to the fear of MMC adverse effects in an operated area or the fear of complications due to perforated bladder. Preliminary results have suggested favourable outcome when MMC is used prior to TURBT [see publication]. To the investigators' knowledge no previous study has prospectively examined the effect of preliminary heated intravesical installation with BWT.
Detailed Description
Scientific hypothesis: Patients treated with preliminary intravesical installation in a timely fashion before TURBT are expected to show lower recurrence rate and better outcome then control patients. Participants: Three hundred patients designed to undergo TURBT in the urology department at "Sheba" Medical Center at "Tel Hashomer", Israel. Exiting the research: Patient is not completing the procedure due to allergic reaction or serious adverse effect during the heated intravesical instillation . Patient having according to pathology report muscle invasive bladder cancer (MIBC) and expects to undergo cystectomy. Protocol steps Eligible patients give their consent to participate in the study. A preliminary grouping (for low, intermediate and high risk groups) will be initiated according to cystoscopy examination results. (this step is for administrative purpose in order to achieve equal amount of participants between groups during follow-up phase) Then participants will randomly assign, according to randomized computer software to two major arms, those who receive the heated thermo-chemo therapy and those who will not. The intravesical instillation will take place up to 6 hours prior TURBT in the following matter: The "Elmedical" system will introduce intravesically a 40mg of heated Mitomycin-C (MMC), diluted in 50cc of saline at a uniform temperature (44-44.50C). The length of the procedure - 50 minutes. Once pathological reports will arrive, the participant will assign to his/her actual risk group stratification. Participants with recurrent disease will be assigned into separated intermediate or high risk groups accordingly. consequently five stratification groups are created in each major research arm (with or without prior heated intravesical instillation) Follow-up of each participant, at any group takes two years. During the follow-up period a urine cytology and routine cystoscopy will be carried out every 3 month. Patients with intermediate to high risk disease will receive six courses of intravesical bacillus Calmette-Guerin (BCG) installation according to international guidelines. Participants who for any reason won't be able to complete the BCG intravesical instillations will be offered a MMC instillation instead. Participant that pathological report is indicating a muscle invasive disease will be offered a cystectomy and exit the study (unless the participant avoids cystectomy by his/her own decision). The investigators are obligate ourselves for surveillance according to international guidelines (as intravesical instillations of BCG or performing repeat TURBT / Biopsy by need). Potential bias: Different surgical skills between urologists, Quality of pre-TURBT installation of thermo-chemotherapy. Duration: Four years with two years follow up per participant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Transitional Cell Carcinoma
Keywords
Recurrence

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
TURBT ONLY
Arm Type
No Intervention
Arm Description
A total of 150 patients in this arm will be divided into five follow-up sub groups according to pathology reports. Group 1 - Primary Low risk patients Group 2 - Primary Intermediate risk patients Group 3 - Primary High risk patients Group 4 - Recurrent Intermediate risk patients Group 5 - Recurrent Intermediate risk patients
Arm Title
BWT with Mitomycin-C prior TURBT
Arm Type
Experimental
Arm Description
A total of 150 patients in this arm will be divided into five follow-up sub groups according to pathology reports. Group 1 - Primary Low risk patients Group 2 - Primary Intermediate risk patients Group 3 - Primary High risk patients Group 4 - Recurrent Intermediate risk patients Group 5 - Recurrent Intermediate risk patients
Intervention Type
Other
Intervention Name(s)
BWT with Mitomycin-C prior TURBT
Other Intervention Name(s)
Bladder wall thermo-chemotherapy (BWT)
Intervention Description
Participants will randomly assign, according to random computerized software, to those who receive the heated thermo-chemo therapy and those who will not. The intravesical instillation will take place up to 6 hours prior TURBT in the following matter: The "Elmedical" BWT system will introduce intravesically a 40mg of heated Mitomycin MMC, diluted in 50cc of saline at a uniform temperature (44-44.50C). The length of the procedure - 50 minutes
Primary Outcome Measure Information:
Title
Recurrence rate of Urothelial carcinoma (UC) of bladder
Description
Reduced recurrence rate of Urothelial carcinoma (UC) of bladder among patients receiving intravesical heated installations
Time Frame
Two years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients (>18 yrs.) with good performance status according to Eastern Cooperative Oncology Group (ECOG) scale, designed to TURBT and gave their consent to participate in our research. All participants must have adequate blood tests (CBC, Creatinine, electrolytes and liver function tests). Exclusion Criteria: Concurrent other malignancy in the urinary system (e.g. upper tract UC) Urothelial malignancy of the bladder other then carcinoma Diffuse carcinoma in situ on preliminary cystoscopy Allergy or sensitivity to MMC Known urinary bladder capacity of less then 200cc Concurrent complicated urinary infection Autoimmune disease or patient under immunosuppressive therapy presence of urethral stricture Previous pelvic radiotherapy Concomitant malignancy of other organ Pregnancy Children under 18 years.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jacob Ramon, Prof.
Phone
+972(0)526666280
Email
jacob.Ramon@sheba.health.gov.il
First Name & Middle Initial & Last Name or Official Title & Degree
Assaf Bar El, Dr.
Phone
+972(0)544664774
Email
assaf.barel@sheba.health.gov.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jacob Ramon, Prof.
Organizational Affiliation
Sheba Medical Center, Department od Urology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheba Medical Center
City
Ramat Gan
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jacob Ramon, M.D
Phone
+9720526666280
Email
jacob.ramon@sheba.health.gov.il
First Name & Middle Initial & Last Name & Degree
Assaf Bar El, M.D
Phone
+972544664774
Email
assaf.barel@sheba.health.gov.il

12. IPD Sharing Statement

Citations:
PubMed Identifier
21831711
Citation
Di Stasi SM, Valenti M, Verri C, Liberati E, Giurioli A, Leprini G, Masedu F, Ricci AR, Micali F, Vespasiani G. Electromotive instillation of mitomycin immediately before transurethral resection for patients with primary urothelial non-muscle invasive bladder cancer: a randomised controlled trial. Lancet Oncol. 2011 Sep;12(9):871-9. doi: 10.1016/S1470-2045(11)70190-5. Epub 2011 Aug 8.
Results Reference
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Intravesically Heated Thermo-chemotherapy With Mitomycin-C Prior to TURBT

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