About this trial
We consecutively enrolled patients presenting with breast space-occupying lesions at our hospital. Medical imaging data from simultaneously acquired ultrafast DCE-MRI, time-dependent diffusion MRI (TDD-MRI), magnetic resonance elastography (MRE), andvirtual magnetic resonance elastography(vMRE), along with clinical and pathological data, were collected. The study aims to evaluate and explore the clinical application value of these multimodal imaging techniques in the precision diagnosis, treatment, and prognosis of breast cancer. The findings are intended to provide a robust imaging basis for formulating and adjusting more precise, individualized treatment plans and prognostic assessments for patients. Ultimately, this research seeks to improve patient quality of life, optimize the allocation of medical resources, and advance the development of precision medicine.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥ 18 years old
Female patients with BI-RADS class 4 or above breast lesions detected by mammography or ultrasound
Perform breast new technology MRI examination (ultra fast DCE-MRI、OGSE 、MRE、vMRE)within one week before biopsy or surgery
Disqualifiers
Previously received breast radiotherapy, chemotherapy, surgery, or targeted therapy
Unable to cooperate in completing MRI examination
The image data contains serious artifacts (such as motion artifacts and metal artifacts), making it impossible to measure parameters
The lesion cannot be clearly identified and outlined on the image
Trial design
Single group
Treatments tested in this trial
The Value of Time-Dependent Diffusion MRI and Magnetic Resonance Elastography in the Precise Diagnosis and Efficacy Assessment of Breast Cancer
Diagnostic testThe MRI scan is part of the standard treatment protocol. Medical imaging data from simultaneously acquired ultrafast DCE-MRI, time-dependent diffusion MRI (TDD-MRI), magnetic resonance elastography (MRE), andvirtual magnetic resonance elastography(vMRE), along with clinical and pathological data, were collected.
Treatment groups
Trial outcomes
Primary outcomes
efficacy evaluation
For patients requiring neoadjuvant therapy, after completing the corresponding cycles of neoadjuvant treatment, the patient's surgical pathology results are used as the gold standard to assess tumor regression and determine whether pathological complete response (pCR) has been achieved.
Differentiation between benign and malignant lesions
With puncture biopsy or surgical pathology serving as the gold standard, MRI parameters are used to distinguish benign from malignant lesions
Sponsors and contacts
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