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Bladder CancerNCT05146635

Optimal Adjuvant Intravesical Therapy for Intermediate Risk Non Muscle Invasive Bladder Cancer: A Randomized Controlled Trial

A study testing Intravesical Bcg and Intravesical chemotherapy (epirubicin) in people with Bladder Cancer, run by Mansoura University at 1 site in Egypt.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The objective of this prospective, single-center randomized controlled trial is to identify the optimal adjuvant intravesical therapy in patients with intermediate risk (IR) non muscle invasive bladder cancer by comparing two commonly utilized intravesical regimens; intravesical immunotherapy (BCG) and intravesical… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Bladder Cancer
What is being tested?
Intravesical Bcg and Intravesical chemotherapy (epirubicin)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
110 participants
Where
1 siteEgypt
Study dates
1 Dec 2021to 1 Jan 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adult patients (aged >18 years)
  • Patients with primary or recurrent papillary NMIBC.
  • Complete TURBT.
  • Patients with IR NMIBC confirmed by histopathology.

Who cannot join

  • Inability to give informed consent.
  • Patients with history of previous radiotherapy or systemic chemotherapy.
  • Patients suffering from immuno-deficiency or other malignancies.
  • Patients with history of hypersensitivity reaction to BCG or epirubicin.
  • Examination under anesthesia (EUA) reveals palpable bladder mass.
  • Patients with low or high risk NMIBC by histopathology

Trial locations and contacts

1 site in 1 country.

Mahmoud Laymon contact

dr_mahmoudlaymon@yahoo.com

Egypt1 site, 1 recruiting
  • Mansoura Urology and Nephrology Center

    Al Mansurah, DK, 35516

    Amr A Elsawy, 01009428750, amrelsawy.unc@hotmail.com

    Mahmoud Laymon, dr_mahmoudlaymon@yahoo.com

    Recruiting

Other trials in Egypt

About this study

The objective of this prospective, single-center randomized controlled trial is to identify the optimal adjuvant intravesical therapy in patients with intermediate risk (IR) non muscle invasive bladder cancer by comparing two commonly utilized intravesical regimens; intravesical immunotherapy (BCG) and intravesical chemotherapy.

Read the detailed description

Bladder cancer (BC) represents a frequent urologic malignancy, and is mainly diagnosed as non-muscle invasive, At presentation, approximately 30% of patients have muscle-invasive BC (clinical T2 or higher) .

Both the natural history of non-muscle-invasive bladder cancer (NMIBC) and its treatment strategies are highly variable. Although some patients never experience disease recurrence, others experience disease progression and eventually die of their disease .

In the absence of intravesical treatment, a patient with non-muscle-invasive BC has a 47% probability of disease recurrence within 5 years of diagnosis and a 9% probability of progression to muscle-invasive disease .

Low-, intermediate- and high-risk categories have been defined to help guide the treatment of patients with NMIBC (Ta, T1, and CIS). Treatment of NMIBC is now relatively well-defined for high-risk and low-risk disease presentation, and awaits further refinement through improvements in therapeutic options .

Solitary low-grade tumors, especially smaller lesions (3 cm or less), respond best to resection and immediate instillation of intravesical agents, whereas higher risk lesions, such as carcinoma in situ and high-grade T1 stage disease, have demonstrated good response to BCG when given on a schedule of induction (an initial 6-week course) and maintenance (3-weekly courses every 6 months for 3 years) .

However, while low- and high-risk diseases have been well-classified, the intermediate-risk (IR) category has traditionally comprised a heterogeneous group of patients that do not fit into either of these categories . As a result, many urologists remain uncertain about the categorization of patients as 'intermediate-risk' as well as the selection of the most appropriate therapeutic option for this patient population .

The pathology of IR NMIBC has been defined by different organizations (American Urological Association, European Association of Urology, National Comprehensive Cancer Network, and International Consultation on Urological Diseases) as those patients with recurrent (<1 year) low-grade Ta disease, solitary low-grade Ta >3cm, multifocal low-grade Ta disease or high-grade Ta disease <3 cm .

Current recommendations for therapy from the aforementioned organizations suggest a basic role for induction and maintenance therapy with either immunotherapy or chemotherapy. Data from a number of recent trials suggest that BCG with maintenance is superior to maintenance chemotherapy in this population as regard to recurrence free survival. On the other hand, no significant benefit of BCG compared with chemotherapy for tumor progression was identified.

Most of these studies were limited by its heterogeneity of patients (non-standardized definition of IR) and non-unified regimen of intravesical treatment (course or utilized chemotherapeutic agent). A well-designed randomized controlled trial with a rigorous methodology is warranted to provide a solid evidence for best practice in this special group of patients.

Conditions
Bladder Cancer
Being tested
Intravesical Bcg, Intravesical chemotherapy (epirubicin)
Keywords
Bladder cancer, Intravesical therapy, Recurrence, Progression
Medical subject headings
Urinary Bladder Neoplasms, Recurrence, Disease Progression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Intravesical BcgDrug

    Patients will receive induction and maintenance BCG after complete TURBT.

  • Intravesical chemotherapy (epirubicin)Drug

    Patients will receive induction and maintenance epirubicin after complete TURBT.

Study groups in NCT05146635
Study groupRoleWhat they receive
Intravesical immunotherapy (BCG) groupActive comparatorNot described
Receives: Drug: Intravesical Bcg
Intravesical chemotherapy (Epirubicin) groupActive comparatorNot described
Receives: Drug: Intravesical chemotherapy (epirubicin)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Tumor recurrence rate

    Number of patient who will develop Recurrence rate during follow up

    Measured: 2 years

  2. Tumor Progression rate

    Number of patient who will develop Progression rate during follow up

    Measured: 2 years

Secondary outcomes (1)
  1. Side effects from intravesical treatments

    Side effects from intravesical treatments

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Dec 2021
  2. Study start1 Dec 2021
  3. Primary completion1 Dec 2022 (estimated)
  4. Study completion1 Jan 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
110 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05146635
Sponsor's protocol ID
AE-12-2021
Status last verified
Dec 2021
First submitted
23 Nov 2021
Last updated
11 Jan 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Intravesical Bcg and Intravesical chemotherapy (epirubicin) in people with Bladder Cancer, run by Mansoura University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 11 Jan 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Amr A Elsawy (01009428750, amrelsawy.unc@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Tumor recurrence rate (time frame: 2 years). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jan 2022.

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