Oncological Outcomes of Different Patterns of Tumor Recurrence at First Evaluation After Bacillus Calmette-Guérin Induction Therapy for Intermediate and High Risk Non Muscle Invasive Bladder Cancer

Sponsor
Mansoura University (Other)
Overall Status
Completed
CT.gov ID
NCT04319263
Collaborator
(none)
1,600
1
1
17
2864.7

Study Details

Study Description

Brief Summary

This retrospective study aimed at assessment of different patterns (morphological and pathological) of tumor recurrence found at first evaluation after BCG induction therapy (3 months cystoscopy) for intermediate and high-risk NMIBC and its prognostic implications at a tertiary referral center.

Condition or Disease Intervention/Treatment Phase
  • Drug: induction regimen of intravesical BCG
N/A

Detailed Description

Bladder cancer (BCa) is the second most common genitourinary malignancy with approximately 75-85% of all patients with BCa present at diagnosis a non-muscle invasive bladder cancer (NMIBC) (Ta, T1 and Tis). Although NMIBC usually carries a favorable prognosis, there is a high risk of disease recurrence and a 10% to 20% risk of progression to muscle-invasive disease.

The common treatment for intermediate- and high-risk patients is a transurethral resection followed by intravesical therapy with bacillus Calmette-Guerin (BCG), a non-specific immunotherapy that has remained the gold standard for 40 years. Over the last decades, several studies have confirmed the superiority of BCG over the combination of epirubicin and interferon, mitomycin C or epirubicin alone for prevention of tumor recurrence, in intermediate- and high-risk tumors.

Despite wide acceptance of BCG intravesical therapy in intermediate and high risk NMIBC, there is still a controversy regarding the optimal protocol of administration. However, most of the guidelines have recommended an induction regimen of six weekly BCG instillations followed by maintenance instillation for at least 1 year.

Complete response (CR) rates after an induction course of BCG for intermediate and high risk NMIBC are high and range from 50-70%. Tumor recurrence at first evaluation (3-months cystoscopy) after BCG induction therapy has been defined as a poor prognostic indicator in those groups of patients with an increased potential risk of disease recurrence and /or progression.

Different patterns of tumor recurrence may be encountered at 3-mo cystoscopy during first evaluation after induction therapy either morphological (single tumor vs. multiple, <3 cm or more, site (? bladder neck involvement), papillary or non papillary) or histopathological (Ta vs. T1, concurrent CIS or not, tumor grade). To determine how to optimally manage those heterogeneous groups of patients, studying of the specific impact of different tumor characteristics on oncological outcomes is warranted.

Study Design

Study Type:
Interventional
Actual Enrollment :
1600 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Oncological Outcomes of Different Patterns of Tumor Recurrence at First Evaluation After Bacillus Calmette-Guérin Induction Therapy for Intermediate and High Risk Non Muscle Invasive Bladder Cancer
Actual Study Start Date :
Mar 1, 2020
Actual Primary Completion Date :
Mar 18, 2020
Actual Study Completion Date :
Mar 18, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: intermediate and high risk non muscle invasive bladder cancer

Drug: induction regimen of intravesical BCG
intravesical instillation of 6 weekly doses of BCG

Outcome Measures

Primary Outcome Measures

  1. one year Recurrence rate [one year]

    recurrence rate at 1 year after induction BCG

  2. one year progression rate [one year]

    progression rate at 1 year after induction BCG

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients for who complete TURBT, was carried out

  • Intermediate and high risk NMIBC.

  • Patients who received full induction BCG regimen (6 weekly doses).

  • Patients completed at least 12 months follow up after 3 months cystoscopy.

Exclusion Criteria:
  • Patients who received incomplete induction BCG regimen (less than 6 weekly doses)

  • Patients with incomplete (less than 12 months) follow up.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Urology and Nephrology Center Mansoura Egypt 35516

Sponsors and Collaborators

  • Mansoura University

Investigators

  • Principal Investigator: Amr A Elsawy, Urology and Nephrology Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Amr Abdel-Lateif El-Sawy, Principal Investigator, Mansoura University
ClinicalTrials.gov Identifier:
NCT04319263
Other Study ID Numbers:
  • AE 20320
First Posted:
Mar 24, 2020
Last Update Posted:
Mar 26, 2020
Last Verified:
Mar 1, 2020
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 26, 2020