Ovarian CancerNCT05697601
Predictors of Ovarian Cancer and Endometrial Cancer for Artificial-Intelligence-Based Screening Tools
An observational study of Ovarian Cancer and Endometrial Cancer, run by Hasanuddin University at 1 site in Indonesia.
Trial summary
The goal of this observational study is to explore the possible associated factors of ovarian cancer and endometrial cancer in Indonesia and develop screening tools that could predict the risk of both types of cancer The specific objectives of the study are 1. Read more about this study
- Who is it for?
- Any age, women onlyHealthy volunteers can take part
- Conditions the study is for
- Ovarian Cancer, Endometrial Cancer, Endometrial Hyperplasia
- What is being tested?
- Artificial-Intelligence Based Screening Tools and Pathology analysis
- How many people
- 2,905 participants
- Where
- 1 siteIndonesia
- Study dates
- 28 Feb 2023to 30 Jun 2024
- 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 Any age
- Women only
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: As this study is utilizing a patient registry, we will involve all eligible participants who undergo gynaecological and pathology assessment for ovarian and endometrial cancer in study centres, based on suggestive signs and symptoms
Who may be able to join
- Women with gynaecological symptoms but not limited to
- Irregular menstruation
- Heavy bleeding during menstruation
- pelvic pain
- vaginal discharge
- sudden weight loss
- pain during sexual intercourse
- Women who underwent routine gynaecological examination
Who cannot join
- unable to undergo serial gynaecological follow-up
Trial locations and contacts
1 site in 1 country.
Indonesia1 site, 1 recruiting
- Recruiting
Hasanuddin University Hospital
Makassar, South Sulawesi, 90245
Bumi Herman, M.D, Ph.D, bumiherman@med.unhas.ac.id
Rina Masadah, MD PhD
About this study
Official title: Associated Factors of Ovarian Cancer and Endometrial Cancer in Indonesia. A Study for Developing Artificial-Intelligence-Based Screening Tools
The goal of this observational study is to explore the possible associated factors of ovarian cancer and endometrial cancer in Indonesia and develop screening tools that could predict the risk of both types of cancer
The specific objectives of the study are
Read more
- Elaborating the situation of ovarian and endometrial cancer in Indonesia
- Exploring the possible clinical, demography and laboratory predictors of these diseases
- Develop artificial-intelligence-based screening tools for both type of cancer based on possible predictors
This study will utilize the patient registry diagnosed with ovarian and endometrial cancer. We assumed that several demography, clinical, and laboratory predictors might possess good screening performance with higher sensitivity and specificity (>80%).
Read the detailed description
Methodology :
This study will involve two different stages
- The first stage will conduct a cohort study to identify the possible predictors of each type of cancer
- The second stage will cover the development of point-of-care testing based on an artificial intelligence model to predict cancer occurrence and prospective testing of the new participants using a diagnostic study method. The tools will predict the current histopathology result and possible future histopathology within one year.
Participants and source of data In the study centre, women with or without gynaecology-associated symptoms underwent gynaecological and pathology assessments to rule out ovarian and endometrial cancer in our study centre were involved. Data is stored digitally and extraction will be done accordingly
Variables and outcome measurement
- Demographic data and health data this information is obtained from the initial assessment of the patients including age, body mass index, chronic diseases, gynaecological and obstetric profile, menstrual pattern, and contraception
- Clinical and laboratory data this include, a complete blood count, selected cancer-associated biomarker (for example Cancer Antigen 125 (Ca-125)), involvement of lymph node, histopathology of pertinent tissues, and signs of metastases through clinical or radiological data
- Outcome final histopathology type and classification assessed by at least two pathologists to determine the type of cancer. The guidelines of classification follow the World Health Organization's classification
Development of Artificial-Intelligence-based screening tools
- The researcher will develop
- an information-based model where the user will provide a response to each predictor
- an image-based model where the user will provide a captured image for prediction
- a mixed-based model where the user can combine captured images and information for each predictor
- proposed model
- scoring-based derived from the coefficient of regression
- decision tree
- random forest
- artificial neural network
- convolutional neural network
- Selection of model
<!-- -->
- Screening performance on split data (or using cross-validation technique)
- evaluation of log-loss or likelihood Timeline
- For the first stage of the study, there will be a time-varying assessment for each participant, however, at least participants undergo an Assessment of all factors and outcomes at baseline. Repeated evaluation as suggested by the physician will be done within one year after the baseline assessment.
- The second study will apply prospective screening. The artificial intelligence-based screening tool will be used concurrently with the gold standard of diagnosis. Possible Bias procedural bias particularly in reliability outcome interpretation is handled by involving multiple pathologists. The pathologist and the screener will perform the screening independently to reduce the tendency of prior results provided by the newly-developed screening tools. Sample size
- The first stage of the research assumes that
- The prevalence of both cancer among all cancers in women accounted for 5% b. Type I error set at 5% c. absolute error of the prevalence 1% using the one-sample proportion formula, the estimated sample size is 1825 participants.
- Following the diagnostic study, we state that the new screening tools model will show non-inferiority performance to histopathology as gold-standard, assuming that
- the expected difference in sensitivity value is 5% assuming that the new screening tools will possess 85% sensitivity and the sensitivity of histopathology is 90% b. cross-over testing will be done, creating an equal allocation of screening intervention c. Type 1 error of the study set at 5% d. Power of the study set at 80% the total sample size for the prospective screening tool will be 1080 participants
Data Quantification and discretization several clinical information will be classified according to the established guideline for example body mass index.
Proposed Statistical Analysis
- Descriptive statistic and bivariate analysis
- A cox-regression will be conducted following the baseline-to-event timeline
- Subgroup analysis will be done, particularly in certain demographic and comorbidity. as for the second stage, the analysis will identify the
- sensitivity
- specificity
- accuracy
- precision
- The number Needed to Treat selected models will be deployed into an application.
- Conditions
- Ovarian Cancer, Endometrial Cancer, Endometrial Hyperplasia
- Being tested
- Artificial-Intelligence Based Screening Tools, Pathology analysis
- Keywords
- Ovarian Cancer, Endometrial Cancer, Endometrial Hyperplasia, Artificial Intelligence, Point of Care Testing, Staging, Gynecological Screening, Pathology
- Medical subject headings
- Ovarian Neoplasms, Endometrial Neoplasms, Endometrial Hyperplasia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Artificial-Intelligence Based Screening ToolsDiagnostic test
Artificial-Intelligence Based Screening Tools build on machine learning models
Pathology analysisDiagnostic test
Pathology assessment of cells and tissues from respective organs
| Study group | Role | What they receive |
|---|---|---|
| Suspect of Ovarian Cancer | The participant with high suspicion of ovarian cancer and undergo gynaecology and pathology assessment Receives: Diagnostic Test: Artificial-Intelligence Based Screening Tools; Diagnostic Test: Pathology analysis | |
| Suspect of Endometrial Cancer | The participant with high suspicion of Endometrial cancer (and or endometrial hyperplasia) and undergo gynaecology and pathology assessment Receives: Diagnostic Test: Artificial-Intelligence Based Screening Tools; Diagnostic Test: Pathology analysis | |
| Normal Cohort | The participant with lower suspicion of both types of cancer and undergo gynaecology and pathology assessment Receives: Diagnostic Test: Artificial-Intelligence Based Screening Tools; Diagnostic Test: Pathology analysis |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of People developing ovarian cancer
Number of people developing ovarian cancer diagnosed with gynaecology and pathology assessment
Measured: from baseline to twelve month after entering cohort
Number of People developing endometrial cancer
Number of people developing endometrial cancer diagnosed with gynaecology and pathology assessment
Measured: from baseline to twelve month after entering cohort
Secondary outcomes (1)
Screening Performance of Artificial-Intelligence-based Screening tools
The sensitivity, specificity, accuracy, precision of selected Artificial-Intelligence-based model to predict the ovarian and/or endometrial cancer
Measured: from baseline assessment up to one year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jan 2023
- Study start28 Feb 2023
- Primary completion28 Feb 2024 (estimated)
- Study completion30 Jun 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (6)Papers the sponsor has linked to this study.
- Other trials for Ovarian 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
- Retrospective
- Enrolment
- 2,905 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hasanuddin University
- Sponsor type
- University, hospital or other
- Collaborators
- Chulalongkorn University
- Responsible party
- Principal investigator, Bumi Herman, Hasanuddin University
- Investigators
- Rina Masadah, Ph.D, Study chair, Hasanuddin UniversityBumi Herman, Ph.D, Principal investigator, Chulalongkorn University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05697601
- Sponsor's protocol ID
- 0901231327
- Status last verified
- Nov 2023
- First submitted
- 14 Jan 2023
- Last updated
- 27 Nov 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: The individual participant data will be shared after de-identification and the purpose of the data utilization is verified by the investigators
Publications
Atallah GA, Abd Aziz NH, Teik CK, Shafiee MN, Kampan NC. New Predictive Biomarkers for Ovarian Cancer. Diagnostics (Basel). 2021 Mar 7;11(3):465. doi: 10.3390/diagnostics11030465.
PubMed 33800113Elias KM, Guo J, Bast RC Jr. Early Detection of Ovarian Cancer. Hematol Oncol Clin North Am. 2018 Dec;32(6):903-914. doi: 10.1016/j.hoc.2018.07.003. Epub 2018 Sep 28.
PubMed 30390764Tanha K, Mottaghi A, Nojomi M, Moradi M, Rajabzadeh R, Lotfi S, Janani L. Investigation on factors associated with ovarian cancer: an umbrella review of systematic review and meta-analyses. J Ovarian Res. 2021 Nov 11;14(1):153. doi: 10.1186/s13048-021-00911-z.
PubMed 34758846Zhao J, Hu Y, Zhao Y, Chen D, Fang T, Ding M. Risk factors of endometrial cancer in patients with endometrial hyperplasia: implication for clinical treatments. BMC Womens Health. 2021 Aug 25;21(1):312. doi: 10.1186/s12905-021-01452-9.
PubMed 34433451Felix AS, Weissfeld JL, Stone RA, Bowser R, Chivukula M, Edwards RP, Linkov F. Factors associated with Type I and Type II endometrial cancer. Cancer Causes Control. 2010 Nov;21(11):1851-6. doi: 10.1007/s10552-010-9612-8. Epub 2010 Jul 14.
PubMed 20628804Herman B, Sirichokchatchawan W, Pongpanich S, Nantasenamat C. Development and performance of CUHAS-ROBUST application for pulmonary rifampicin-resistance tuberculosis screening in Indonesia. PLoS One. 2021 Mar 25;16(3):e0249243. doi: 10.1371/journal.pone.0249243. eCollection 2021.
PubMed 33765092
Study at a glance
From the registry record, last updated by the sponsor on 27 Nov 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Associated Factors of Ovarian Cancer and Endometrial Cancer in Indonesia. A Study for Developing Artificial-Intelligence-Based Screening Tools
- ClinicalTrials.gov ID
- NCT05697601
- Acronym / sponsor ID
- 0901231327
- Conditions
- Ovarian Cancer, Endometrial Cancer, Endometrial Hyperplasia
- Keywords
- Ovarian Cancer, Endometrial Cancer, Endometrial Hyperplasia, Artificial Intelligence, Point of Care Testing, Staging, Gynecological Screening, Pathology
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 2,905 participants (estimated)
- Lead sponsor
- Hasanuddin UniversityUniversity, hospital or other
- Collaborators
- Chulalongkorn University
- Study start
- 28 Feb 2023 (actual)
- Primary completion
- 28 Feb 2024 (estimated)
- Study completion
- 30 Jun 2024 (estimated)
- First posted
- 26 Jan 2023 (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.
The goal of this observational study is to explore the possible associated factors of ovarian cancer and endometrial cancer in Indonesia and develop screening tools that could predict the risk of both types of cancer
The specific objectives of the study are
- Elaborating the situation of ovarian and endometrial cancer in Indonesia
- Exploring the possible clinical, demography and laboratory predictors of these diseases
- Develop artificial-intelligence-based screening tools for both type of cancer based on possible predictors
This study will utilize the patient registry diagnosed with ovarian and endometrial cancer. We assumed that several demography, clinical, and laboratory predictors might possess good screening performance with higher sensitivity and specificity (>80%).
Detailed description
Methodology :
This study will involve two different stages
- The first stage will conduct a cohort study to identify the possible predictors of each type of cancer
- The second stage will cover the development of point-of-care testing based on an artificial intelligence model to predict cancer occurrence and prospective testing of the new participants using a diagnostic study method. The tools will predict the current histopathology result and possible future histopathology within one year.
Participants and source of data In the study centre, women with or without gynaecology-associated symptoms underwent gynaecological and pathology assessments to rule out ovarian and endometrial cancer in our study centre were involved. Data is stored digitally and extraction will be done accordingly
Variables and outcome measurement
- Demographic data and health data this information is obtained from the initial assessment of the patients including age, body mass index, chronic diseases, gynaecological and obstetric profile, menstrual pattern, and contraception
- Clinical and laboratory data this include, a complete blood count, selected cancer-associated biomarker (for example Cancer Antigen 125 (Ca-125)), involvement of lymph node, histopathology of pertinent tissues, and signs of metastases through clinical or radiological data
- Outcome final histopathology type and classification assessed by at least two pathologists to determine the type of cancer. The guidelines of classification follow the World Health Organization's classification
Development of Artificial-Intelligence-based screening tools
- The researcher will develop
- an information-based model where the user will provide a response to each predictor
- an image-based model where the user will provide a captured image for prediction
- a mixed-based model where the user can combine captured images and information for each predictor
- proposed model
- scoring-based derived from the coefficient of regression
- decision tree
- random forest
- artificial neural network
- convolutional neural network
- Selection of model
<!-- -->
- Screening performance on split data (or using cross-validation technique)
- evaluation of log-loss or likelihood Timeline
- For the first stage of the study, there will be a time-varying assessment for each participant, however, at least participants undergo an Assessment of all factors and outcomes at baseline. Repeated evaluation as suggested by the physician will be done within one year after the baseline assessment.
- The second study will apply prospective screening. The artificial intelligence-based screening tool will be used concurrently with the gold standard of diagnosis. Possible Bias procedural bias particularly in reliability outcome interpretation is handled by involving multiple pathologists. The pathologist and the screener will perform the screening independently to reduce the tendency of prior results provided by the newly-developed screening tools. Sample size
- The first stage of the research assumes that
- The prevalence of both cancer among all cancers in women accounted for 5% b. Type I error set at 5% c. absolute error of the prevalence 1% using the one-sample proportion formula, the estimated sample size is 1825 participants.
- Following the diagnostic study, we state that the new screening tools model will show non-inferiority performance to histopathology as gold-standard, assuming that
- the expected difference in sensitivity value is 5% assuming that the new screening tools will possess 85% sensitivity and the sensitivity of histopathology is 90% b. cross-over testing will be done, creating an equal allocation of screening intervention c. Type 1 error of the study set at 5% d. Power of the study set at 80% the total sample size for the prospective screening tool will be 1080 participants
Data Quantification and discretization several clinical information will be classified according to the established guideline for example body mass index.
Proposed Statistical Analysis
- Descriptive statistic and bivariate analysis
- A cox-regression will be conducted following the baseline-to-event timeline
- Subgroup analysis will be done, particularly in certain demographic and comorbidity. as for the second stage, the analysis will identify the
- sensitivity
- specificity
- accuracy
- precision
- The number Needed to Treat selected models will be deployed into an application.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Suspect of Ovarian Cancer | – | Diagnostic Test: Artificial-Intelligence Based Screening Tools, Diagnostic Test: Pathology analysisThe participant with high suspicion of ovarian cancer and undergo gynaecology and pathology assessment |
| Suspect of Endometrial Cancer | – | Diagnostic Test: Artificial-Intelligence Based Screening Tools, Diagnostic Test: Pathology analysisThe participant with high suspicion of Endometrial cancer (and or endometrial hyperplasia) and undergo gynaecology and pathology assessment |
| Normal Cohort | – | Diagnostic Test: Artificial-Intelligence Based Screening Tools, Diagnostic Test: Pathology analysisThe participant with lower suspicion of both types of cancer and undergo gynaecology and pathology assessment |
Who may qualify
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- As this study is utilizing a patient registry, we will involve all eligible participants who undergo gynaecological and pathology assessment for ovarian and endometrial cancer in study centres, based on suggestive signs and symptoms
Key inclusion criteria (8 listed)
- Women with gynaecological symptoms but not limited to
- Women who underwent routine gynaecological examination
Key exclusion criteria (1 listed)
- unable to undergo serial gynaecological follow-up
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 |
|---|---|---|
| Artificial-Intelligence Based Screening ToolsArtificial-Intelligence Based Screening Tools build on machine learning models | Diagnostic test | Normal Cohort, Suspect of Endometrial Cancer, Suspect of Ovarian Cancer |
| Pathology analysisPathology assessment of cells and tissues from respective organs | Diagnostic test | Normal Cohort, Suspect of Endometrial Cancer, Suspect of Ovarian Cancer |
Primary outcome
Number of People developing ovarian cancer
Time frame: from baseline to twelve month after entering cohort
Number of people developing ovarian cancer diagnosed with gynaecology and pathology assessment
Number of People developing endometrial cancer
Time frame: from baseline to twelve month after entering cohort
Number of people developing endometrial cancer diagnosed with gynaecology and pathology assessment
1 secondary outcome
Screening Performance of Artificial-Intelligence-based Screening tools
Time frame: from baseline assessment up to one year
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Nov 2023.
- Background: PubMed 33800113Atallah GA, Abd Aziz NH, Teik CK, Shafiee MN, Kampan NC. New Predictive Biomarkers for Ovarian Cancer. Diagnostics (Basel). 2021 Mar 7;11(3):465. doi: 10.3390/diagnostics11030465.
- Background: PubMed 30390764Elias KM, Guo J, Bast RC Jr. Early Detection of Ovarian Cancer. Hematol Oncol Clin North Am. 2018 Dec;32(6):903-914. doi: 10.1016/j.hoc.2018.07.003. Epub 2018 Sep 28.
- Background: PubMed 34758846Tanha K, Mottaghi A, Nojomi M, Moradi M, Rajabzadeh R, Lotfi S, Janani L. Investigation on factors associated with ovarian cancer: an umbrella review of systematic review and meta-analyses. J Ovarian Res. 2021 Nov 11;14(1):153. doi: 10.1186/s13048-021-00911-z.
- Background: PubMed 34433451Zhao J, Hu Y, Zhao Y, Chen D, Fang T, Ding M. Risk factors of endometrial cancer in patients with endometrial hyperplasia: implication for clinical treatments. BMC Womens Health. 2021 Aug 25;21(1):312. doi: 10.1186/s12905-021-01452-9.
- Background: PubMed 20628804Felix AS, Weissfeld JL, Stone RA, Bowser R, Chivukula M, Edwards RP, Linkov F. Factors associated with Type I and Type II endometrial cancer. Cancer Causes Control. 2010 Nov;21(11):1851-6. doi: 10.1007/s10552-010-9612-8. Epub 2010 Jul 14.
- Background: PubMed 33765092Herman B, Sirichokchatchawan W, Pongpanich S, Nantasenamat C. Development and performance of CUHAS-ROBUST application for pulmonary rifampicin-resistance tuberculosis screening in Indonesia. PLoS One. 2021 Mar 25;16(3):e0249243. doi: 10.1371/journal.pone.0249243. eCollection 2021.
- Individual participant dataSharing planned: No. The individual participant data will be shared after de-identification and the purpose of the data utilization is verified by the investigators
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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.
Rina Masadah, Ph.D study chair
Hasanuddin University
Bumi Herman, Ph.D principal investigator
Chulalongkorn 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 Ovarian Cancer and Endometrial Cancer, run by Hasanuddin University at 1 site in Indonesia.
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 8 inclusion and 1 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 27 Nov 2023. 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 Indonesia. 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 Bumi Herman, Ph.D (+66638275008, bumi.h@chula.ac.th), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of People developing ovarian cancer (time frame: from baseline to twelve month after entering cohort). 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?
On the ClinicalTrials.gov record for NCT05697601, which also lists 6 linked publications.
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 27 Nov 2023.