Breast CancerNCT07389200
Application of Multimodal MRI-based Radiomics in Histological Grading and Prognostic Assessment of Breast Cancer
An observational study of Breast Cancer and Breast Cancer With Low to Intermediate HER2 Expression, run by Hao Xu.
Trial summary
In addition to TNM staging, the current management of breast cancer is based on conventional pathological features that categorize the disease into three molecular subtypes, each with significant prognostic implications in clinical practice: human epidermal growth factor receptor 2 (HER2)-positive, luminal (hormone… Read more about this study
- Who is it for?
- Any age, women only
- Conditions the study is for
- Breast Cancer, Breast Cancer With Low to Intermediate HER2 Expression
- What is being tested?
- DCE-MRI
- How many people
- 400 participants
- Where
- No sites listed yet
- Study dates
- 1 Jan 2028to 30 Dec 2029
- How long will I take part?
- 400 Months
- Phase
- Observational
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
- No healthy volunteers
- Child, Adult, Older adult
Study population: 368 female patients diagnosed with breast cancer from three hospitals between August 2017 and December 2021 were consecutively recruited in this study
Who may be able to join
- Histopathological diagnosis of breast cancer by surgical or biopsy pathology;
- Availability of DCE-MRI within two weeks before surgery
- No prior treatment before baseline DCE-MRI examination.
Who cannot join
- Less than 5 mm of long diameter of the lesion
- Severe motion artifacts
- Missing or incomplete essential data
- Anti-tumor treatment before MRI
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
In addition to TNM staging, the current management of breast cancer is based on conventional pathological features that categorize the disease into three molecular subtypes, each with significant prognostic implications in clinical practice: human epidermal growth factor receptor 2 (HER2)-positive, luminal (hormone receptor-positive and HER2-negative), and triple-negative breast cancers. The overexpression or amplification of HER2 is observed in 10-15% of breast cancer cases. This phenomenon often correlates with a more aggressive tumor behavior while also demonstrating an increased responsiveness to HER2-targeted therapies. However, the use of highly effective anti-HER2 drugs can significantly enhance the survival outcomes of these patients. Additionally, the expression status of HER2 is critical in determining the necessity for targeted therapy. Therefore, preoperative assessment of HER2 expression status has important therapeutic implications. Currently, clinical methods for assessing HER2 status in breast cancer before surgery include immunohistochemistry (IHC) tests and fluorescence in situ hybridization (FISH) measurements performed on core-needle biopsy specimens. However, these biopsy sampling techniques have inherent limitations, including sampling bias and an inability to fully represent intratumor heterogeneity. Additionally, the biopsy procedure can be uncomfortable and carries certain risks for patients. Tumour heterogeneity generally refers to the variations in angiogenesis, metabolism, gene expression, and other biological characteristics among tumors. Intratumoral heterogeneity (ITH) can manifest as signal differences in radiological images at the macro level. Investigators hypothesized that significant differences in biological characteristics and behavior exist between HER2-positive (HER2+) and HER2-negative (HER2 -) breast cancers, allowing for the distinction of these two types of tumours by identifying specific imaging features that reflect ITH.
Dynamic contrast-enhanced MRI (DCE-MRI) is an effective imaging modality that provides temporal information regarding the dynamics of contrast agents in suspicious lesions while maintaining acceptable spatial resolution. It is particularly sensitive in detecting breast cancer lesions, especially those in dense breast tissue. DCE-MRI can indirectly reflect abnormal tumor vascular proliferation through the hemodynamic characteristics of the lesions. Radiomics is an emerging technology that involves extracting quantitative and reproducible features from medical images using high-throughput, sophisticated modalities that are often challenging to identify or quantify visually. These features, which may be linked to specific diseases, are analyzed using statistical or machine learning (ML) algorithms to create predictive models for tumor diagnosis, grading, efficacy evaluation, and prognosis prediction. ML has two important advantages over traditional statistical models. The goal is to reduce decision time during diagnosis and generally achieve greater diagnostic accuracy. As demonstrated in breast cancer diagnosis, ML can significantly improve cancer risk prediction by identifying complex patterns in large amounts of clinical data. Despite the great potential of ML, it still faces several obstacles in its clinical application. A major challenge is a lack of interpretability-many ML models operate like "black boxes", making it difficult for clinicians to understand and trust their decision-making processes. Furthermore, the performance of the model depends heavily on the quality and representativeness of the training data. ML methods often require larger data sets than traditional clinical studies.
Thus, this study aimed to develop a radiomics-based ML model that could predict the HER2 status of breast cancers in a non-invasive manner using DCE-MRI images. Additionally, the Shapley Additive Explanation (SHAP) algorithm was employed to analyze the contribution of the variables included in the model, providing valuable insights for formulating more accurate preoperative treatment plans for patients with breast cancers.
- Being tested
- DCE-MRI
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DCE-MRIOther
Patients at Hospital 1 underwent DCE-MRI using a 16-channel breast coil on a 3.0-T MRI scanner (Skyra, Siemens Healthcare, Erlangen, Germany) for the training and internal validation set. The external validation set comprised patients from Hospital 2 (GE Signa HDxt, equipped with a dedicated 7-channel phased-array breast coil) and Hospital 3 (Ingenia, Philips, Amsterdam, the Netherlands, also featuring a dedicated 7-channel phased-array breast coil)
| Study group | Role | What they receive |
|---|---|---|
| Breast Cancer | Not described Receives: Other: DCE-MRI |
What is being measured
The primary outcome is the main question the study is designed to answer.
Patients with pathologically confirmed breast cancer who underwent DCE-MRI were included. Radiomic features were extracted, and seven machine learning algorithms were utilized to construct predictive model.The AUC served as the evaluation metric
The AUC served as the primary evaluation metric for identifying the optimal model. A comprehensive model evaluation was conducted, which included AUC, accuracy, sensitivity, specificity
Measured: From enrollment to the end of treatment at 8 weeks
F1 score
F1 score, with validation on an independent cohort.
Measured: From enrollment to the end of treatment at 8 weeks
Secondary outcomes (1)
histopathological diagnosis of breast cancer by surgical or biopsy pathology
Measured: From enrollment to the end of treatment at 8 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Feb 2026
- Study start1 Jan 2028 (estimated)
- Primary completion30 Dec 2029 (estimated)
- Study completion30 Dec 2029 (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
- Other
- Enrolment
- 400 participants (estimated)
- Target duration
- 400 Months
Sponsor and investigators
- Lead sponsor
- Hao Xu
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Hao Xu, Sichuan Cancer Hospital and Research Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07389200
- Sponsor's protocol ID
- SCCSMC-01-2024-119
- Status last verified
- Jan 2026
- First submitted
- 10 Jan 2026
- Last updated
- 5 Feb 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No