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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.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

Bumi Herman, Ph.D contact

+66638275008

bumi.h@chula.ac.th

Indonesia1 site, 1 recruiting
  • Hasanuddin University Hospital

    Makassar, South Sulawesi, 90245

    Bumi Herman, M.D, Ph.D, bumiherman@med.unhas.ac.id

    Rina Masadah, MD PhD

    Recruiting

Other trials in Indonesia

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
  1. Elaborating the situation of ovarian and endometrial cancer in Indonesia
  2. Exploring the possible clinical, demography and laboratory predictors of these diseases
  3. 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

  1. The first stage will conduct a cohort study to identify the possible predictors of each type of cancer
  2. 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

  1. 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
  2. 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
  3. 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

  1. 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
  1. proposed model
  • scoring-based derived from the coefficient of regression
  • decision tree
  • random forest
  • artificial neural network
  • convolutional neural network
  1. Selection of model

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  1. Screening performance on split data (or using cross-validation technique)
  2. evaluation of log-loss or likelihood Timeline
  3. 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.
  4. 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
  5. The first stage of the research assumes that
  6. 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.
  7. Following the diagnostic study, we state that the new screening tools model will show non-inferiority performance to histopathology as gold-standard, assuming that
  8. 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

  1. Descriptive statistic and bivariate analysis
  2. A cox-regression will be conducted following the baseline-to-event timeline
  3. Subgroup analysis will be done, particularly in certain demographic and comorbidity. as for the second stage, the analysis will identify the
  4. sensitivity
  5. specificity
  6. accuracy
  7. precision
  8. The number Needed to Treat selected models will be deployed into an application.
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 groups in NCT05697601
Study groupRoleWhat they receive
Suspect of Ovarian CancerThe 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 CancerThe 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 CohortThe 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.

  1. 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

  2. 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)
  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.

  1. First posted26 Jan 2023
  2. Study start28 Feb 2023
  3. Primary completion28 Feb 2024 (estimated)
  4. Study completion30 Jun 2024 (estimated)

Resources

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)
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 33800113
  • Elias 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 30390764
  • Tanha 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 34758846
  • Zhao 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 34433451
  • Felix 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 20628804
  • Herman 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

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.

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