A Proposed Tetra-modal Treatment Protocol for Muscle Invasive Urothelial Carcinoma of the Urinary Bladder

Sponsor
Assiut University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05503563
Collaborator
(none)
50
1
26.1
1.9

Study Details

Study Description

Brief Summary

In Egypt, bladder cancer has been the most common cancer during the past 50 years. In 2002, Egypt's world-standardized bladder cancer incidence was 37/ 100,000, representing approximately 30,000 new cases each year.

About 25% of new diagnoses are muscle-invasive bladder cancer (MIBC), which carry a worse prognosis compared to non-muscle invasive disease.

Neoadjuvant chemotherapy (NAC) followed by radical cystectomy (RC) with bilateral pelvic lymphadenectomy is considered the standard of care for treatment of MIBC by multiple international guidelines.

However, this is associated with a significant impact on quality of life.

The effect of our proposed Tetra-modal treatment protocol for muscle invasive Urothelial carcinoma of the urinary bladder on muscle invasive bladder cancer recurrence free survival, cancer specific survival, and overall survival?

Koga developed a selective bladder-sparing protocol with a tetra modal therapy comprising maximal transurethral resection of bladder tumor, induction chemoradiation (CRT), and consolidative partial cystectomy (PC) with pelvic lymph node dissection, allowing the confirmation of CRT response pathologically. In the preliminary analysis of the initial cases enrolled in their protocol, none of the patients who completed the protocol with consolidative PC experienced MIBC recurrence, suggesting that consolidative PC may improve local cancer control in the preserved bladder by surgically eliminating possible cancer remnants after CRT.

Our proposed Tetra-modal treatment protocol for MIBC is supposed to eliminate the surgical difficulties of performing PC in a radiated field and hence decrease the post operative complications of PC.

Condition or Disease Intervention/Treatment Phase
  • Procedure: terta modal bladder preservation

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Proposed Tetra-modal Treatment Protocol for Muscle Invasive Urothelial Carcinoma of the Urinary Bladder
Actual Study Start Date :
Jul 15, 2022
Anticipated Primary Completion Date :
Sep 15, 2024
Anticipated Study Completion Date :
Sep 15, 2024

Arms and Interventions

Arm Intervention/Treatment
tetra modal bladder preservation

Procedure: terta modal bladder preservation
neoadjuvant chemotherapy, partial cystectomy, radiotherapy

Outcome Measures

Primary Outcome Measures

  1. local recurrence rate [the patient will be evaluted after partial cystectomy every 3 months for 2 years]

    the patient will be evaluated using MRI and cystoscopy

  2. over active bladder symptom score [this questionnaire will be carried every 6 month for at least 2 years after the partial cystectomy]

    the patient will be asked about his symptoms using a questionnaire that is concerned about urgency , frequency , urge incontinence .

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Tumor size ≤ 50 % of bladder surface or multiple tumors in an area of the bladder that is ≤ 50 % of total bladder surface.

  2. Tumor at least 2 cm away from bladder neck or trigone.

  3. Clinically, no residual disease or minimal amounts of non-invasive disease in the original MIBC site after NAC at restaging TURBT (if done).

  4. Pathologically confirmed urothelial carcinoma.

Exclusion Criteria:
  1. Prescence of CIS.

  2. Presence of distant metastasis.

  3. Patients unfit for cisplatin-based chemotherapy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assuit university Assiut Assuit Egypt 71511

Sponsors and Collaborators

  • Assiut University

Investigators

  • Study Director: Diaa A Sayed, PhD, cheif of urological oncology department

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Abdelrahman Atef Ali, Urologist at Assuit University Hospital, Assiut University
ClinicalTrials.gov Identifier:
NCT05503563
Other Study ID Numbers:
  • AssuitUUro
First Posted:
Aug 16, 2022
Last Update Posted:
Aug 16, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Abdelrahman Atef Ali, Urologist at Assuit University Hospital, Assiut University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 16, 2022