Non-Muscle Invasive Bladder CancerNCT05332353
Machine Learning-Based Prediction of BCG Response in High-Risk Non-Muscle Invasive Bladder Cancer Patients
An observational study of Non-Muscle Invasive Bladder Cancer, run by Mansoura University at 1 site in Egypt.
Trial summary
This prospective study aims at using Artificial intelligence to create a helpful unbiased machine learning-based model that predicts BCG unresponsiveness in high risk BCG-naïve NMIBC patients incorporating all potential clinico-pathological, radiological and/or molecular prognostic factors. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Non-Muscle Invasive Bladder Cancer
- What is being tested?
- Bacillus Calmette-Guerin
- How many people
- 100 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Apr 2022to 1 Dec 2023
- How long will I take part?
- 6 Months
- Phase
- Observational
- 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
Study population: Patients with diagnosed bladder tumors seen through the outpatient clinic in the urology department, Urology and Nephrology Center (Mansoura University, Egypt) will be assessed for eligibility. Patients who are meeting these criteria will be asked to participate in this prospective study and will be provided with an informed consent form. all patients will be thoroughly evaluated by medical history and physical examination, routine laboratory investigations, mpMRI lower abdomen and pelvis. Then, all patients will be managed by complete TURBT followed by re-staging TUR biopsy after 2-6 weeks. All included patients will be discharged to receive adjuvant intravesical BCG therapy and to be followed-up according to the predetermined protocol.
Who may be able to join
- Ability to give informed consent.
- High-risk NMIBC (any patient with high grade Ta or high grade T1 or CIS or recurrent multiple large tumors with low grade Ta/T1)
- Good performance status (Defined as: performance status 0 or 1 at the time of TURBT according to Eastern Cooperative Oncology Group-ECOG-).
- No prior history of BCG intravesical therapy.
Who cannot join
- History of previous radiotherapy or systemic chemotherapy.
- Post TURBT histopathology report showing any of the following;
- Benign histopathology.
- Muscle invasive urothelial carcinoma.
- Non urothelial carcinoma of the bladder.
Trial locations and contacts
1 site in 1 country.
Egypt1 site, 1 recruiting
- Recruiting
Urology and Nephrology Center
Al Mansurah, Outside U.S./Canada, 35511
Osama Ezzat, Ass. lect., 01023990432, osamaezzat1990@gmail.com
About this study
This prospective study aims at using Artificial intelligence to create a helpful unbiased machine learning-based model that predicts BCG unresponsiveness in high risk BCG-naïve NMIBC patients incorporating all potential clinico-pathological, radiological and/or molecular prognostic factors.
Read the detailed description
Introduction:
In the era of BCG shortage and BCG-associated morbidity, the development of prognostic models remains a never-ending topic of research to predict Non Muscle Invasive Bladder Cancer (NMIBC) patients of high risk of BCG unresponsiveness; hence optimize their treatment, achieve survival benefit with minimal long-term morbidity, and prioritize patients with expected good response.
Aim of the study:
This prospective study aims at using Artificial intelligence to create a helpful unbiased machine learning-based model that predicts BCG unresponsiveness in high risk BCG-naïve NMIBC patients incorporating all potential clinico-pathological, radiological and/or molecular prognostic factors.
Patients and Methods:
Patients with diagnosed bladder tumors seen through the outpatient clinic in the urology department (Urology and Nephrology Center, Mansoura University, Egypt) will be assessed for eligibility to the study and inclusion criteria (Ability to give informed consent, High-risk NMIBC, Good performance status and No prior history of BCG intravesical therapy) then asked to participate in this prospective study via an informed consent form.
All patients will be thoroughly evaluated by medical history and physical examination, routine laboratory investigations (including cytology and N/L ratio), mpMRI lower abdomen and pelvis and molecular markers evaluation (Urinary IL-10 levels by solid phase ELISA Immunoassay, Reverse Transcriptase-quantitative Polymerase Chain Reaction (RT qPCR) technology-based assessment of serum TNF-a and Chromosomal anomalies using FISH technique) . Then, all patients will be managed by cystoscopy and initial complete TURBTfollowed by re-staging TUR biopsy 2-6 weeks later on. All patients will be discharged after the re-staging TUR to receive adjuvant intravesical BCG therapy in the outpatient clinic and to be followed-up according to the predetermined protocol. If any patient has new tumour/positive cytology by outpatient cystoscopy after ICR, he will be readmitted to our center and subjected to cystoscopic-guided biopsy. If high grade or CIS proven pathology, BCG unresponsiveness will be considered. Univariate and multivariate analysis will be performed to identify independent prognostic factors associated with BCG unresponsiveness. After that, each of these factors will have a score according to its regression coefficient. Then, these independent factors with their scores will be summed into Artificial Neural Network-based prediction model for predicting BCG unresponsiveness.
Sample size and statistical analysis:
Sample size is calculated for the final analysis 6 months post initial TURBT with α = 0.05 (adjusted for the primary outcome which is BCG unresponsiveness) and a power of 80% (β = 0.20). A sample size of 45 patients per group should be available for final analysis. Since an overall dropout rate of about 10% is expected, 50 patients per group have to be recruited. All statistical analyses will be performed using ABM SPSS program version 20.
Ethical considerations:
A fully informed consent will be taken from all patients. The study will approved by the local ethical committee IRB (Institutional review board), faculty of medicine, Mansoura University. Patients will be managed according to Declaration of Helsinki.
- Conditions
- Non-Muscle Invasive Bladder Cancer
- Being tested
- Bacillus Calmette-Guerin
- Keywords
- Machine Learning, BCG Response, Prediction, Non-Muscle Invasive Bladder Cancer
- Medical subject headings
- Non-Muscle Invasive Bladder Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Bacillus Calmette-GuerinDrug
Also called BCG
Bacillus Calmette-Guerin (BCG) is immunotherapy to prevent recurrence and progression of non muscle invasive bladder cancer.
| Study group | Role | What they receive |
|---|---|---|
| BCG responders | Non-muscle invasive bladder cancer patients who do not have T1/Ta HG recurrence within 6 months of adequate BCG therapy. Receives: Drug: Bacillus Calmette-Guerin | |
| BCG non-responders | Non-muscle invasive bladder cancer patients who have T1/Ta HG recurrence within 6 months of adequate BCG therapy or CIS within 12 months of BCG therapy Receives: Drug: Bacillus Calmette-Guerin |
What is being measured
The primary outcome is the main question the study is designed to answer.
BCG unresponsiveness
T1/Ta HG recurrence within 6 months of adequate BCG therapy
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Apr 2022
- Study start1 Apr 2022
- Primary completion1 Dec 2022 (estimated)
- Study completion1 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-Muscle Invasive Bladder CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 100 participants (estimated)
- Target duration
- 6 Months
Sponsor and investigators
- Lead sponsor
- Mansoura University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Osama Ezzat Mohammed Attia, Mansoura University
- Investigators
- Osama Ezzat, Ass. lect., Principal investigator, urology and nephrology center mansoura university
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05332353
- Sponsor's protocol ID
- MD.22.03.622
- Status last verified
- Apr 2022
- First submitted
- 11 Apr 2022
- Last updated
- 18 Apr 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided: protocol of the study as well as data of our patients will be available and shared by the end of the study
Study at a glance
From the registry record, last updated by the sponsor on 18 Apr 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Machine Learning-Based Prediction of BCG Response in High-Risk Non-Muscle Invasive Bladder Cancer Patients
- ClinicalTrials.gov ID
- NCT05332353
- Acronym / sponsor ID
- MD.22.03.622
- Conditions
- Non-Muscle Invasive Bladder Cancer
- Keywords
- Machine Learning, BCG Response, Prediction, Non-Muscle Invasive Bladder Cancer
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Mansoura UniversityUniversity, hospital or other
- Study start
- 1 Apr 2022 (actual)
- Primary completion
- 1 Dec 2022 (estimated)
- Study completion
- 1 Dec 2023 (estimated)
- First posted
- 18 Apr 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This prospective study aims at using Artificial intelligence to create a helpful unbiased machine learning-based model that predicts BCG unresponsiveness in high risk BCG-naïve NMIBC patients incorporating all potential clinico-pathological, radiological and/or molecular prognostic factors.
Detailed description
Introduction:
In the era of BCG shortage and BCG-associated morbidity, the development of prognostic models remains a never-ending topic of research to predict Non Muscle Invasive Bladder Cancer (NMIBC) patients of high risk of BCG unresponsiveness; hence optimize their treatment, achieve survival benefit with minimal long-term morbidity, and prioritize patients with expected good response.
Aim of the study:
This prospective study aims at using Artificial intelligence to create a helpful unbiased machine learning-based model that predicts BCG unresponsiveness in high risk BCG-naïve NMIBC patients incorporating all potential clinico-pathological, radiological and/or molecular prognostic factors.
Patients and Methods:
Patients with diagnosed bladder tumors seen through the outpatient clinic in the urology department (Urology and Nephrology Center, Mansoura University, Egypt) will be assessed for eligibility to the study and inclusion criteria (Ability to give informed consent, High-risk NMIBC, Good performance status and No prior history of BCG intravesical therapy) then asked to participate in this prospective study via an informed consent form.
All patients will be thoroughly evaluated by medical history and physical examination, routine laboratory investigations (including cytology and N/L ratio), mpMRI lower abdomen and pelvis and molecular markers evaluation (Urinary IL-10 levels by solid phase ELISA Immunoassay, Reverse Transcriptase-quantitative Polymerase Chain Reaction (RT qPCR) technology-based assessment of serum TNF-a and Chromosomal anomalies using FISH technique) . Then, all patients will be managed by cystoscopy and initial complete TURBTfollowed by re-staging TUR biopsy 2-6 weeks later on. All patients will be discharged after the re-staging TUR to receive adjuvant intravesical BCG therapy in the outpatient clinic and to be followed-up according to the predetermined protocol. If any patient has new tumour/positive cytology by outpatient cystoscopy after ICR, he will be readmitted to our center and subjected to cystoscopic-guided biopsy. If high grade or CIS proven pathology, BCG unresponsiveness will be considered. Univariate and multivariate analysis will be performed to identify independent prognostic factors associated with BCG unresponsiveness. After that, each of these factors will have a score according to its regression coefficient. Then, these independent factors with their scores will be summed into Artificial Neural Network-based prediction model for predicting BCG unresponsiveness.
Sample size and statistical analysis:
Sample size is calculated for the final analysis 6 months post initial TURBT with α = 0.05 (adjusted for the primary outcome which is BCG unresponsiveness) and a power of 80% (β = 0.20). A sample size of 45 patients per group should be available for final analysis. Since an overall dropout rate of about 10% is expected, 50 patients per group have to be recruited. All statistical analyses will be performed using ABM SPSS program version 20.
Ethical considerations:
A fully informed consent will be taken from all patients. The study will approved by the local ethical committee IRB (Institutional review board), faculty of medicine, Mansoura University. Patients will be managed according to Declaration of Helsinki.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 6 Months
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| BCG responders | – | Drug: Bacillus Calmette-GuerinNon-muscle invasive bladder cancer patients who do not have T1/Ta HG recurrence within 6 months of adequate BCG therapy. |
| BCG non-responders | – | Drug: Bacillus Calmette-GuerinNon-muscle invasive bladder cancer patients who have T1/Ta HG recurrence within 6 months of adequate BCG therapy or CIS within 12 months of BCG therapy |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with diagnosed bladder tumors seen through the outpatient clinic in the urology department, Urology and Nephrology Center (Mansoura University, Egypt) will be assessed for eligibility. Patients who are meeting these criteria will be asked to participate in this prospective study and will be provided with an informed consent form. all patients will be thoroughly evaluated by medical history and physical examination, routine laboratory investigations, mpMRI lower abdomen and pelvis. Then, all patients will be managed by complete TURBT followed by re-staging TUR biopsy after 2-6 weeks. All included patients will be discharged to receive adjuvant intravesical BCG therapy and to be followed-up according to the predetermined protocol.
Key inclusion criteria (4 listed)
- Ability to give informed consent.
- High-risk NMIBC (any patient with high grade Ta or high grade T1 or CIS or recurrent multiple large tumors with low grade Ta/T1)
- Good performance status (Defined as: performance status 0 or 1 at the time of TURBT according to Eastern Cooperative Oncology Group-ECOG-).
- No prior history of BCG intravesical therapy.
Key exclusion criteria (5 listed)
- History of previous radiotherapy or systemic chemotherapy.
- Post TURBT histopathology report showing any of the following;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Bacillus Calmette-GuerinAlso: BCGBacillus Calmette-Guerin (BCG) is immunotherapy to prevent recurrence and progression of non muscle invasive bladder cancer. | Drug | BCG non-responders, BCG responders |
Primary outcome
BCG unresponsiveness
Time frame: 6 months
T1/Ta HG recurrence within 6 months of adequate BCG therapy
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Apr 2022.
- Individual participant dataSharing planned: Undecided. protocol of the study as well as data of our patients will be available and shared by the end of the study
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Testing the Addition of an Anti-cancer Drug, Pembrolizumab, to the Usual Intravesical Chemotherapy Treatment (Gemcitabine) for the Treatment of BCG-Unresponsive Non-muscle Invasive Bladder Cancer
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Efficacy and Safety of Pembrolizumab (MK-3475) in Combination With Bacillus Calmette-Guerin (BCG) in High-Risk Non-Muscle Invasive Bladder Cancer (HR NMIBC) (MK-3475-676/KEYNOTE-676)
High-risk Non-muscle Invasive Bladder Cancer
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Antibody-Drug Conjugate Plus Immunotherapy Versus Immunotherapy Plus Chemotherapy for Extensive Transurethrally Unresectable Very-High-Risk Non-Muscle-Invasive Bladder Cancer
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Osama Ezzat, Ass. lect. principal investigator
urology and nephrology center mansoura university
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Non-Muscle Invasive 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 5 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 18 Apr 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 Osama Ezzat, Ass. lect. (01023990432, osamaezzat1990@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
BCG unresponsiveness (time frame: 6 months). 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 18 Apr 2022.