search
Back to results

Effectiveness of an Immediate Postoperative Intravesical Instillation With Either Gemcitabine or Epirubicin in Patients With Urinary Bladder Cancer (Gemcitabine Epirubicin Normal SAline) (GENSA)

Primary Purpose

Bladder Cancer

Status
Recruiting
Phase
Phase 3
Locations
Greece
Study Type
Interventional
Intervention
Gemcitabine Hydrochloride combined with continuous saline irrigation
Epirubicin Hydrochloride combined with continuous saline irrigation
Sponsored by
University of Thessaly
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Bladder Cancer focused on measuring Postoperative intravesical instillation, Gemcitabine, Epirubicin

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary urinary bladder tumor
  • Secondary urinary bladder tumor (recurrence)
  • Bipolar or monopolar resection
  • Creat <2.2mg/dl
  • 35% <Hct <52%
  • White bloode cells count WBC ≥3000 / μL
  • 75000 <PLT <500000 / μL
  • Urine culture: negative / sterile
  • Alkaline phosphatase, total bilirubin, SGOT, SGPT: values as high as 2 times above the upper normal limit
  • Good clinical condition (according to Eastern Cooperative Oncology Group PS ≤ 1)
  • CT Urography without findings suggesting an upper urinary tract tumor in the last 3 months before the transurethral resection of the bladder tumor

Exclusion Criteria:

  • More than 2 low grade / high differentiation (low grade / LG) histologically confirmed bladder tumors in the last 18 months before the transurethral resection of the bladder tumor
  • High grade / low differentiation (HG) histologically confirmed bladder tumor in the last 9 months before the transurethral resection of the bladder tumor
  • Those who undergo a transurethral resection of a bladder tumor according to the Guidelines of the European Association of Urology for non-muscle-invasive bladder cancer: incomplete resection of tumor, absence of muscle fibers in the sample with the exception of: Ta / LG-G1, primary Cis and finally, pT1 tumors
  • Intravesical instillation of chemotherapeutic agent or BCG in the last 6 months before the transurethral resection of the bladder tumor
  • History of non-urothelial bladder cancer
  • Stage of disease pT2 (muscle-invasive bladder cancer)
  • Presence of a tumor in the urethra
  • Upper urinary tract malignancy (present or anamnestically)
  • History of pelvic radiotherapy
  • Histrory of another malignancy in the last 5 years before the transurethral resection of the bladder tumor

Sites / Locations

  • Urology Department, University of Thessaly, University Hospital of LarissaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Gemcitabine

Epirubicin

Arm Description

Bladder cancer patients, who are treated with a transurethral resection of a bladder tumor, receive postoperatively, within 6 hours after the resection, an immediate single intravesical instillation with gemcitabine hydrochloride 2gr in 100ml of saline for 45-60 minutes and continuous saline irrigation for 24 hours

Bladder cancer patients, who are treated with a transurethral resection of a bladder tumor, receive postoperatively, within 6 hours after the resection, an immediate single intravesical instillation with epirubicine hydrochloride 50mg in 50ml of saline for 45-60 minutes and continuous saline irrigation for 24 hours

Outcomes

Primary Outcome Measures

Bladder cancer recurrence
Histologically proven bladder cancer recurrence
Bladder cancer progression
Histologically proven bladder cancer progression
Bladder cancer recurrence
Histologically proven bladder cancer recurrence
Bladder cancer progression
Histologically proven bladder cancer progression

Secondary Outcome Measures

Bladder cancer recurrence
Histologically proven bladder cancer recurrence
Bladder cancer progression
Histologically proven bladder cancer progression

Full Information

First Posted
June 17, 2021
Last Updated
January 25, 2022
Sponsor
University of Thessaly
search

1. Study Identification

Unique Protocol Identification Number
NCT04947059
Brief Title
Effectiveness of an Immediate Postoperative Intravesical Instillation With Either Gemcitabine or Epirubicin in Patients With Urinary Bladder Cancer (Gemcitabine Epirubicin Normal SAline)
Acronym
GENSA
Official Title
A Prospective Phase III Randomized Clinical Trial Comparing the Effectiveness of Immediate Postoperative Intravesical Instillation With Either Gemcitabine Hydrochloride or Epirubicin Hydrochloride in Patients With Urinary Bladder Cancer (Gemcitabine Epirubicin Normal SAline)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 14, 2021 (Actual)
Primary Completion Date
October 2025 (Anticipated)
Study Completion Date
October 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Thessaly

4. Oversight

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

5. Study Description

Brief Summary
The natural history of non-muscle-invasive bladder cancer is characterised by recurrence and progression. We compare the effectiveness of gemcitabine hydrochloride and epirubicin hydrochloride, in combination with continuous saline irrigation, as an immediate single intravesical instillation in the potential reduction of the disease recurrence as well as progression.
Detailed Description
Bladder cancer (BLCa) is the seventh most commonly diagnosed cancer in the male population worldwide, while it drops to tenth when both genders are considered. At diagnosis about 75% of the patients suffer from non-muscle-invasive BLCa. The natural history of this disease is characterised by recurrence and progression. In order to reduce the possibilities for recurrence, and therefore progression, an immediate single intravesical instillation (ISIVI) of a chemotherapeutic agent has been shown to act by destroying circulating tumour cells after transurethral resection of urinary bladder tumors (TURB), and by an ablative effect on residual tumour cells at the resection site and on small overlooked tumours. Several agents, among them gemcitabine and epirubicin, have been used for the ISIVI so far. Moreover, four large meta-analyses comprising 1,476 to 3,103 patients have consistently shown that after TURB, ISIVI significantly reduces the recurrence rate compared to TURB alone. Furthermore, two meta-analyses suggest efficacy of continuous saline irrigation (CSI) in the prevention of early recurrences. The prevention of tumour cell implantation should be initiated within the first few hours after TURB. After that, tumour cells are firmly implanted and are covered by the extracellular matrix. In all ISIVI studies, the instillation was administered within 24 hours. Until today, no randomised comparisons of individual drugs, combined or not with CSI, have been conducted. After the initial TURB, the patients will be treated with CSI for 24 hours. Then, they will be randomised, either to gemcitabine or epirubicin, and within 6 hours after the TURB they will receive an ISIVI with gemcitabine or epirubicin, as follows: - GROUP A: Gemcitabine hydrochloride 2gr in 100ml 0.9% NaCl for 45-60 minutes - GROUP B: Epirubicin hydrochloride 50mg in 50ml 0.9% NaCl for 45-60 minutes During the ISIVI the CSI will be stopped. The ISIVI will not be applied in the following cases: Active bleeding, which does not allow to interrupt the CSI Postoperative fever > 38°C Deep resection of the tumor, which could be associated with bladder perforation and therefore potential extravasation of the administered drug Known allergy to gemcitabine or epirubicin The postoperative follow-up for patients with disease stage pTis, Ta, T1 low grade (LG) / high grade (HG), will be done according to the Guidelines of the European Association of Urology (EAU) for non-muscle-invasive bladder cancer, as follows: 1st and 2nd year: Cystoscopy & cytological examination of urine every 3 months, CT Urography every 12 months for HG patients 3rd year: Cystoscopy & cytological examination of urine every 6 months, CT Urography every 12 months for HG patients

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer
Keywords
Postoperative intravesical instillation, Gemcitabine, Epirubicin

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Bladder cancer patients, who are treated with a transurethral resection of the bladder tumor, receive postoperatively an immediate single intravesical instillation with either gemcitabine hydrochloride or epirubicine hydrochloride
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gemcitabine
Arm Type
Active Comparator
Arm Description
Bladder cancer patients, who are treated with a transurethral resection of a bladder tumor, receive postoperatively, within 6 hours after the resection, an immediate single intravesical instillation with gemcitabine hydrochloride 2gr in 100ml of saline for 45-60 minutes and continuous saline irrigation for 24 hours
Arm Title
Epirubicin
Arm Type
Active Comparator
Arm Description
Bladder cancer patients, who are treated with a transurethral resection of a bladder tumor, receive postoperatively, within 6 hours after the resection, an immediate single intravesical instillation with epirubicine hydrochloride 50mg in 50ml of saline for 45-60 minutes and continuous saline irrigation for 24 hours
Intervention Type
Drug
Intervention Name(s)
Gemcitabine Hydrochloride combined with continuous saline irrigation
Other Intervention Name(s)
GROUP A
Intervention Description
Immediate single intravesical instillation with gemcitabine combined with continuous saline irrigation in bladder cancer patients who are treated with a transurethral resection of the tumor
Intervention Type
Drug
Intervention Name(s)
Epirubicin Hydrochloride combined with continuous saline irrigation
Other Intervention Name(s)
GROUP B
Intervention Description
Immediate single intravesical instillation with epirubicin combined with continuous saline irrigation in bladder cancer patients who are treated with a transurethral resection of the tumor
Primary Outcome Measure Information:
Title
Bladder cancer recurrence
Description
Histologically proven bladder cancer recurrence
Time Frame
At 3 months after the transurethral resection of a bladder tumor
Title
Bladder cancer progression
Description
Histologically proven bladder cancer progression
Time Frame
At 3 months after the transurethral resection of a bladder tumor
Title
Bladder cancer recurrence
Description
Histologically proven bladder cancer recurrence
Time Frame
At 12 months after the transurethral resection of a bladder tumor
Title
Bladder cancer progression
Description
Histologically proven bladder cancer progression
Time Frame
At 12 months after the transurethral resection of a bladder tumor
Secondary Outcome Measure Information:
Title
Bladder cancer recurrence
Description
Histologically proven bladder cancer recurrence
Time Frame
At 24 months after the transurethral resection of a bladder tumor
Title
Bladder cancer progression
Description
Histologically proven bladder cancer progression
Time Frame
At 24 months after the transurethral resection of a bladder tumor

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary urinary bladder tumor Secondary urinary bladder tumor (recurrence) Bipolar or monopolar resection Creat <2.2mg/dl 35% <Hct <52% White bloode cells count WBC ≥3000 / μL 75000 <PLT <500000 / μL Urine culture: negative / sterile Alkaline phosphatase, total bilirubin, SGOT, SGPT: values as high as 2 times above the upper normal limit Good clinical condition (according to Eastern Cooperative Oncology Group PS ≤ 1) CT Urography without findings suggesting an upper urinary tract tumor in the last 3 months before the transurethral resection of the bladder tumor Exclusion Criteria: More than 2 low grade / high differentiation (low grade / LG) histologically confirmed bladder tumors in the last 18 months before the transurethral resection of the bladder tumor High grade / low differentiation (HG) histologically confirmed bladder tumor in the last 9 months before the transurethral resection of the bladder tumor Those who undergo a transurethral resection of a bladder tumor according to the Guidelines of the European Association of Urology for non-muscle-invasive bladder cancer: incomplete resection of tumor, absence of muscle fibers in the sample with the exception of: Ta / LG-G1, primary Cis and finally, pT1 tumors Intravesical instillation of chemotherapeutic agent or BCG in the last 6 months before the transurethral resection of the bladder tumor History of non-urothelial bladder cancer Stage of disease pT2 (muscle-invasive bladder cancer) Presence of a tumor in the urethra Upper urinary tract malignancy (present or anamnestically) History of pelvic radiotherapy Histrory of another malignancy in the last 5 years before the transurethral resection of the bladder tumor
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vasileios Tzortzis, Professor
Phone
00302413502811
Email
urologydpt.uth@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Lampros Mitrakas, Consultant
Phone
00302413501325
Email
lamprosmit@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vasileios Tzortzis, Professor
Organizational Affiliation
Urology Department, University of Thessaly, University Hospital of Larissa, Greece
Official's Role
Principal Investigator
Facility Information:
Facility Name
Urology Department, University of Thessaly, University Hospital of Larissa
City
Larissa
State/Province
Larissa/Thessaly
ZIP/Postal Code
41110
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vasileios Tzortzis, Professor
Phone
00302413502811
Email
urologydpt.uth@gmail.com
First Name & Middle Initial & Last Name & Degree
Lampros Mitrakas, Consultant
Phone
00302413501325
Email
lamprosmit@gmail.com
First Name & Middle Initial & Last Name & Degree
Vasileios Tzortzis, Professor
First Name & Middle Initial & Last Name & Degree
Lampros Mitrakas, Consultant

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All IPD that underlie results in a publication
IPD Sharing Time Frame
After a publication and for a period of 2 years

Learn more about this trial

Effectiveness of an Immediate Postoperative Intravesical Instillation With Either Gemcitabine or Epirubicin in Patients With Urinary Bladder Cancer (Gemcitabine Epirubicin Normal SAline)

We'll reach out to this number within 24 hrs