Breast CancerNCT07752238
Diagnostic Prediction Model for De Novo Metastatic Breast Cancer
An observational study of Breast Cancer and Metastatic Invasive Breast Cancer, run by Markusovszky University Teaching Hospital os County Vas at 1 site in Hungary.
Trial summary
The goal of this observational study is to create a tool to estimate the risk of macroscopic distant tumor spread in women with newly diagnosed breast cancer. The main question it aims to answer is: Can a model, which combines routine medical information collected at diagnosis, accurately predict if a patient has… Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Breast Cancer, Metastatic Invasive Breast Cancer
- How many people
- 925 participants
- Where
- 1 siteHungary
- Study dates
- 10 Aug 2026to 28 Feb 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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
- Women only
- No healthy volunteers
- Adult, Older adult
Study population: A consecutive cohort of adult female patients with newly diagnosed invasive breast cancer.
Who may be able to join
- Female sex, aged 18 years or older.
- Newly diagnosed invasive breast cancer.
- Case reviewed by the Multidisciplinary Tumour Board at the study site during the inclusion period (between October 1, 2018, and July 31, 2025).
- No history of prior or synchronous invasive malignancies, except for synchronous bilateral breast cancer.
- Intent for primary treatment and clinical management at the study site.
- Availability of longitudinal clinical records throughout the 12-month follow-up period or until death.
Who cannot join
- -Absence of baseline systemic staging.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Hungary1 site, 1 recruiting
- Recruiting
Markusovszky University Teaching Hospital
Szombathely, Vas County, 9700
Oliver Laszlo Stari, MD, 011-36-94-311542, stari.oliver@gmail.com
About this study
Official title: Development of a Diagnostic Prediction Model for de Novo Metastatic Breast Cancer Using Routinely Available Baseline Parameters
The goal of this observational study is to create a tool to estimate the risk of macroscopic distant tumor spread in women with newly diagnosed breast cancer. The main question it aims to answer is:
- Can a model, which combines routine medical information collected at diagnosis, accurately predict if a patient has metastasis large enough to be found during systemic imaging? Researchers will review the past medical records of participants who were treated at a university hospital. Because this study looks at past data, participants will not be asked to do any new tasks, take new tests, or change their medical care.
Read the detailed description
BACKGROUND AND RATIONALE
Baseline risk assessment traditionally relies on anatomical extent, while intrinsic tumour aggressiveness is established as a key determinant of distant spread. In addition, the systemic inflammatory response is increasingly recognized as a driver of tumour progression. The evaluation of these diverse and often conflicting factors complicates early clinical decision-making.
OBJECTIVE
The objective of this study is to develop and internally validate a multivariable diagnostic prediction model using routinely available baseline parameters to estimate the individualised probability of macroscopic distant metastasis among patients with newly diagnosed invasive breast cancer.
STUDY DESIGN AND SETTING
This is an investigator-initiated, single-centre, retrospective cohort study adhering to the TRIPOD+AI statement. The study is conducted at a university teaching hospital, where comprehensive baseline systemic staging is the institutional standard for all newly diagnosed breast cancer patients.
PREDICTORS
The model integrates routinely available baseline parameters: clinical tumor size, clinical lymphnode status, the Ki-67 proliferation marker, and a composite systemic inflammatory marker (Pan-immune-inflammation value).
DATA COLLECTION AND QUALITY ASSURANCE
Data extraction is performed independently by two multidisciplinary teams. Any discrepancies are resolved through a formal adjudication process by an expert panel not involved in data collection (senior oncologist, radiologist, pathologist, and surgeon).
SAMPLE SIZE AND MISSING DATA Based on the criteria proposed by Riley et al., the study requires a minimum of 925 participants and 93 events to accommodate maximum model complexity. Missing data will be handled using complete-case analysis if the rate is <5%, or multiple imputation if >5%.
STATISTICAL ANALYSIS AND MODEL DEVELOPMENT
For the multivariable logistic regression model, all pre-specified predictors are entered simultaneously. Continuous variables are retained in their continuous form. Non-linear relationships modeled using restricted cubic splines. Model performance is evaluated via discrimination and calibration metrics, while clinical utility is assessed through decision curve analysis. Internal validation is conducted using bootstrapping. To correct for model optimism, a global shrinkage factor based on the bootstrap calibration slope is applied. Instability plots are used to illustrate the stability of predictions, calibration, and net benefit.
PATIENT AND PUBLIC INVOLVEMENT (PPI)
To initiate Patient and Public Involvement, an inaugural patient engagement event will be held to discuss the clinical acceptability of a diagnostic prediction model and its potential role in shared decision-making. This event will serve as the foundation to establish a voluntary Patient Advisory Group (PAG). In subsequent project stages, the newly formed PAG will collaborate to co-produce a Plain Language Summary and explore potential pathways for the tool's future clinical application.
- Conditions
- Breast Cancer, Metastatic Invasive Breast Cancer
- Keywords
- de novo metastasis, breast cancer, predictive modelling
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Primary study cohort | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
De novo metastatic breast cancer
A newly diagnosed breast cancer with distant spread identified at baseline systemic staging. Distant lesions are categorized as de novo metastasis if confirmed via biopsy, secondary imaging, follow-up imaging, or Multidisciplinary Tumor Board consensus based on definitive clinical evidence. Equivocal cases are adjudicated through a review of the 12 month clinical follow-up.
Measured: From the initial diagnostic mammogram up to 12 months of follow-up.
Secondary outcomes (3)
Incidence of rapid metastatic recurrence
Patients developing systemic spread within the 12-month follow-up period, subsequent to an initially negative baseline systemic staging. Patients with rapid metastatic recurrence are excluded from the multivariable analysis and reported descriptively.
Measured: Up to 12 months from the initial diagnostic mammogram.
Systemic staging interval
The time elapsed from the initial diagnostic mammogram to the completion of baseline systemic staging.
Measured: Up to 12 months from the initial diagnostic mammogram.
Diagnostic interval
The time elapsed from the initial diagnostic mammogram to the confirmation of macroscopic distant metastasis.
Measured: Up to 12 months from the initial diagnostic mammogram.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Aug 2026
- Study start10 Aug 2026
- Primary completion31 Oct 2026 (estimated)
- Study completion28 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Breast 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
- 925 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Markusovszky University Teaching Hospital os County Vas
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Oliver Laszlo Stari, Markusovszky University Teaching Hospital os County Vas
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07752238
- Sponsor's protocol ID
- VAS-RKEB/BNJ-6/2026
- Status last verified
- Aug 2026
- First submitted
- 3 Aug 2026
- Last updated
- 12 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: A complete, cleaned, and de-identified copy of the final dataset will be shared. Sensitive data types, including digital images, specific event dates, and demographic details other than categorical age groups, will be redacted.
Study at a glance
From the registry record, last updated by the sponsor on 12 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Development of a Diagnostic Prediction Model for de Novo Metastatic Breast Cancer Using Routinely Available Baseline Parameters
- ClinicalTrials.gov ID
- NCT07752238
- Acronym / sponsor ID
- VAS-RKEB/BNJ-6/2026
- Conditions
- Breast Cancer, Metastatic Invasive Breast Cancer
- Keywords
- de novo metastasis, breast cancer, predictive modelling
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 925 participants (estimated)
- Lead sponsor
- Markusovszky University Teaching Hospital os County VasUniversity, hospital or other
- Study start
- 10 Aug 2026 (actual)
- Primary completion
- 31 Oct 2026 (estimated)
- Study completion
- 28 Feb 2027 (estimated)
- First posted
- 7 Aug 2026 (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 create a tool to estimate the risk of macroscopic distant tumor spread in women with newly diagnosed breast cancer. The main question it aims to answer is:
- Can a model, which combines routine medical information collected at diagnosis, accurately predict if a patient has metastasis large enough to be found during systemic imaging? Researchers will review the past medical records of participants who were treated at a university hospital. Because this study looks at past data, participants will not be asked to do any new tasks, take new tests, or change their medical care.
Detailed description
BACKGROUND AND RATIONALE
Baseline risk assessment traditionally relies on anatomical extent, while intrinsic tumour aggressiveness is established as a key determinant of distant spread. In addition, the systemic inflammatory response is increasingly recognized as a driver of tumour progression. The evaluation of these diverse and often conflicting factors complicates early clinical decision-making.
OBJECTIVE
The objective of this study is to develop and internally validate a multivariable diagnostic prediction model using routinely available baseline parameters to estimate the individualised probability of macroscopic distant metastasis among patients with newly diagnosed invasive breast cancer.
STUDY DESIGN AND SETTING
This is an investigator-initiated, single-centre, retrospective cohort study adhering to the TRIPOD+AI statement. The study is conducted at a university teaching hospital, where comprehensive baseline systemic staging is the institutional standard for all newly diagnosed breast cancer patients.
PREDICTORS
The model integrates routinely available baseline parameters: clinical tumor size, clinical lymphnode status, the Ki-67 proliferation marker, and a composite systemic inflammatory marker (Pan-immune-inflammation value).
DATA COLLECTION AND QUALITY ASSURANCE
Data extraction is performed independently by two multidisciplinary teams. Any discrepancies are resolved through a formal adjudication process by an expert panel not involved in data collection (senior oncologist, radiologist, pathologist, and surgeon).
SAMPLE SIZE AND MISSING DATA Based on the criteria proposed by Riley et al., the study requires a minimum of 925 participants and 93 events to accommodate maximum model complexity. Missing data will be handled using complete-case analysis if the rate is <5%, or multiple imputation if >5%.
STATISTICAL ANALYSIS AND MODEL DEVELOPMENT
For the multivariable logistic regression model, all pre-specified predictors are entered simultaneously. Continuous variables are retained in their continuous form. Non-linear relationships modeled using restricted cubic splines. Model performance is evaluated via discrimination and calibration metrics, while clinical utility is assessed through decision curve analysis. Internal validation is conducted using bootstrapping. To correct for model optimism, a global shrinkage factor based on the bootstrap calibration slope is applied. Instability plots are used to illustrate the stability of predictions, calibration, and net benefit.
PATIENT AND PUBLIC INVOLVEMENT (PPI)
To initiate Patient and Public Involvement, an inaugural patient engagement event will be held to discuss the clinical acceptability of a diagnostic prediction model and its potential role in shared decision-making. This event will serve as the foundation to establish a voluntary Patient Advisory Group (PAG). In subsequent project stages, the newly formed PAG will collaborate to co-produce a Plain Language Summary and explore potential pathways for the tool's future clinical application.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Primary study cohort | – | – |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- A consecutive cohort of adult female patients with newly diagnosed invasive breast cancer.
Key inclusion criteria (6 listed)
- Female sex, aged 18 years or older.
- Newly diagnosed invasive breast cancer.
- Case reviewed by the Multidisciplinary Tumour Board at the study site during the inclusion period (between October 1, 2018, and July 31, 2025).
- No history of prior or synchronous invasive malignancies, except for synchronous bilateral breast cancer.
- Intent for primary treatment and clinical management at the study site.
Key exclusion criteria (1 listed)
- -Absence of baseline systemic staging.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
De novo metastatic breast cancer
Time frame: From the initial diagnostic mammogram up to 12 months of follow-up.
A newly diagnosed breast cancer with distant spread identified at baseline systemic staging. Distant lesions are categorized as de novo metastasis if confirmed via biopsy, secondary imaging, follow-up imaging, or Multidisciplinary Tumor Board consensus based on definitive clinical evidence. Equivocal cases are adjudicated through a review of the 12 month clinical follow-up.
3 secondary outcomes
Incidence of rapid metastatic recurrence
Time frame: Up to 12 months from the initial diagnostic mammogram.
Systemic staging interval
Time frame: Up to 12 months from the initial diagnostic mammogram.
Diagnostic interval
Time frame: Up to 12 months from the initial diagnostic mammogram.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Aug 2026.
- Individual participant dataSharing planned: Yes. A complete, cleaned, and de-identified copy of the final dataset will be shared. Sensitive data types, including digital images, specific event dates, and demographic details other than categorical age groups, will be redacted.
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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.
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 Breast Cancer and Metastatic Invasive Breast Cancer, run by Markusovszky University Teaching Hospital os County Vas at 1 site in Hungary.
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 6 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: looking for participants now, as of the sponsor's last update on 12 Aug 2026. 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 Hungary. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Oliver L Stari, MD (011-36-94-311542, stari.oliver@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
De novo metastatic breast cancer (time frame: From the initial diagnostic mammogram up to 12 months of follow-up.). 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 12 Aug 2026.