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临床试验/NCT07598084
NCT07598084尚未招募不适用

Artificial Intelligence Solution for Simplifying the Diagnostic Workflow of Breast MRI: Development and Clinical Validation of a Diffusion-Weighted Imaging-Based Synthetic Contrast-Enhanced MRI System for Non-Contrast Breast Cancer Diagnosis and Risk Stratification

Peking University People's Hospital0 个研究点目标入组 12,000 人开始时间: 2026年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
12,000
主要终点
MRI examination

研究概览

简要总结

This study is conducted under the ethics-approved project titled "Artificial Intelligence Solution for Simplifying the Diagnostic Workflow of Breast MRI''.The goal of this observational study is to develop an integrated breast MRI system that uses diffusion-weighted imaging (DWI) to create synthetic contrast-enhanced images. This system aims to diagnose and screen for breast cancer without the need for contrast agents, while using a generated risk score to perform imaging-based triage and risk stratification.

Participants will include people aged 18 and older who require a breast MRI either for evaluation of a suspicious finding or for high-risk screening.

This study seeks to answer two main questions:

  • Can synthetic contrast-enhanced images generated from DWI match real contrast-enhanced images in their ability to distinguish benign from malignant breast lesions?
  • Can the risk score derived from DWI-based synthetic images enable imaging-level risk stratification, allowing people at lower risk to avoid contrast agent injection? Researchers will compare the quality of synthetic images against real contrast-enhanced images and will recruit radiologists to assess how well these images perform for diagnostic and screening tasks. MRI data from participants undergoing breast MRI will be used to train, validate, and test this integrated system.

详细描述

We selected "other" in Time Perspective. This study will retrospectively collect MRI data from patients who underwent breast MRI at multiple centers between 2014 and 2024. We will also prospectively enroll MRI data from multiple centers for testing to assess the model's robustness.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Complete breast MRI data;
  • Negative pathology biopsy results or negative follow-up examinations for at least 12 months for non-cancer cases;
  • Positive biopsy results that meet the requirements for the pathological subtype of cancer for cancer cases;
  • Original data that can be used to verify clinical status, including radiological and pathological reports;

排除标准

  • Partial mastectomy or puncture biopsy on the diseased side of the breast prior to breast MRI examination;
  • Poor image quality;
  • Implants in the affected breast;

研究组 & 干预措施

External test cohort E

Participants were retrospectively collected from center E. All participants have completed the MRI examination and have available images for evaluation. All enrolled data will be used for the model testing.

干预措施: Non-contrast breast MRI diagnostic model (Diagnostic Test)

Training cohort

Participants were retrospectively collected from Peking university people's hospital. All participants have completed the MRI examination and have available images for evaluation.

干预措施: Non-contrast breast MRI diagnostic model (Diagnostic Test)

External test cohort A

Participants were retrospectively collected from Center A. All participants have completed the MRI examination and have available images for evaluation. All enrolled data will be used for the model testing.

干预措施: Non-contrast breast MRI diagnostic model (Diagnostic Test)

External test cohort B

Participants were retrospectively collected from center B. All participants have completed the MRI examination and have available images for evaluation. All enrolled data will be used for the model testing.

干预措施: Non-contrast breast MRI diagnostic model (Diagnostic Test)

External test cohort C

Participants were retrospectively collected from center C. All participants have completed the MRI examination and have available images for evaluation. All enrolled data will be used for the model testing.

干预措施: Non-contrast breast MRI diagnostic model (Diagnostic Test)

External test cohort D

Participants were retrospectively collected from center D. All participants have completed the MRI examination and have available images for evaluation. All enrolled data will be used for the model testing.

干预措施: Non-contrast breast MRI diagnostic model (Diagnostic Test)

External test cohort F

Participants were prospectively enrolled from Center F. All participants will undergo MRI examination and have available images for evaluation. All enrolled data will be used for the model testing.

External test cohort G

Participants were prospectively enrolled from Peking University People's Hospital. All participants will undergo MRI examination and have images available for evaluation. All enrolled data will be used for the model testing.

干预措施: Non-contrast breast MRI diagnostic model (Diagnostic Test)

结局指标

主要结局

MRI examination

时间窗: Baseline

A multi-parameter contrast-enhanced breast MRI examination was performed, including fat-suppressed T2-weighted imaging, diffusion-weighted imaging, dynamic contrast-enhanced sequences, and fat-suppressed T1-weighted imaging.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Wang Yi

Professor

Peking University People's Hospital

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