Non-Contrast Breast MRI Diagnosis and Risk Stratification Using DWI-Generated Synthetic Contrast Enhancement
5 июня 2026 г. обновлено: Wang Yi, Peking University People's Hospital
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
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.
Обзор исследования
Статус
Еще не набирают
Условия
Вмешательство/лечение
Подробное описание
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.
Тип исследования
Наблюдательный
Регистрация (Оцененный)
12000
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Контакты исследования
- Имя: HAOQUAN CHEN, MD
- Номер телефона: +86 010-88325811
- Электронная почта: CHENHAOQUANSZ@163.COM
Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
- Пожилой взрослый
Принимает здоровых добровольцев
Да
Метод выборки
Вероятностная выборка
Исследуемая популяция
Participants who underwent breast MR examinations at five institutions from 2014 to 2024 were enrolled.
A test cohort prospectively collected at Peking University People's Hospital Health Examination Center, was enrolled to assess the robustness of the model.
Описание
Inclusion Criteria:
- 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;
Exclusion Criteria:
- 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;
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
Когорты и вмешательства
Группа / когорта |
Вмешательство/лечение |
|---|---|
|
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.
|
An integrated AI model capable of generating synthetic contrast-enhanced images and distinguishing between benign and malignant lesions, as well as performing risk stratification
|
|
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.
|
An integrated AI model capable of generating synthetic contrast-enhanced images and distinguishing between benign and malignant lesions, as well as performing risk stratification
|
|
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.
|
An integrated AI model capable of generating synthetic contrast-enhanced images and distinguishing between benign and malignant lesions, as well as performing risk stratification
|
|
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.
|
An integrated AI model capable of generating synthetic contrast-enhanced images and distinguishing between benign and malignant lesions, as well as performing risk stratification
|
|
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.
|
An integrated AI model capable of generating synthetic contrast-enhanced images and distinguishing between benign and malignant lesions, as well as performing risk stratification
|
|
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.
|
An integrated AI model capable of generating synthetic contrast-enhanced images and distinguishing between benign and malignant lesions, as well as performing risk stratification
|
|
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.
|
An integrated AI model capable of generating synthetic contrast-enhanced images and distinguishing between benign and malignant lesions, as well as performing risk stratification
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
MRI examination
Временное ограничение: 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.
|
Baseline
|
Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Публикации и полезные ссылки
Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.
Общие публикации
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- Wang P, Wang H, Nie P, Dang Y, Liu R, Qu M, Wang J, Mu G, Jia T, Shang L, Zhu K, Feng J, Chen B. Enabling AI-Generated Content for Gadolinium-Free Contrast-Enhanced Breast Magnetic Resonance Imaging. J Magn Reson Imaging. 2025 Mar;61(3):1232-1243. doi: 10.1002/jmri.29528. Epub 2024 Jul 25.
- Chung M, Calabrese E, Mongan J, Ray KM, Hayward JH, Kelil T, Sieberg R, Hylton N, Joe BN, Lee AY. Deep Learning to Simulate Contrast-enhanced Breast MRI of Invasive Breast Cancer. Radiology. 2023 Mar;306(3):e239004. doi: 10.1148/radiol.239004. No abstract available.
- Youn I, Biswas D, Hippe DS, Winter AM, Kazerouni AS, Javid SH, Lee JM, Rahbar H, Partridge SC. Diagnostic Performance of Point-of-Care Apparent Diffusion Coefficient Measures to Reduce Biopsy in Breast Lesions at MRI: Clinical Validation. Radiology. 2024 Feb;310(2):e232313. doi: 10.1148/radiol.232313.
- Witowski J, Heacock L, Reig B, Kang SK, Lewin A, Pysarenko K, Patel S, Samreen N, Rudnicki W, Luczynska E, Popiela T, Moy L, Geras KJ. Improving breast cancer diagnostics with deep learning for MRI. Sci Transl Med. 2022 Sep 28;14(664):eabo4802. doi: 10.1126/scitranslmed.abo4802. Epub 2022 Sep 28.
- Amornsiripanitch N, Bickelhaupt S, Shin HJ, Dang M, Rahbar H, Pinker K, Partridge SC. Diffusion-weighted MRI for Unenhanced Breast Cancer Screening. Radiology. 2019 Dec;293(3):504-520. doi: 10.1148/radiol.2019182789. Epub 2019 Oct 8.
- Baltzer A, Dietzel M, Kaiser CG, Baltzer PA. Combined reading of Contrast Enhanced and Diffusion Weighted Magnetic Resonance Imaging by using a simple sum score. Eur Radiol. 2016 Mar;26(3):884-91. doi: 10.1007/s00330-015-3886-x. Epub 2015 Jun 27.
- Rahbar H, Zhang Z, Chenevert TL, Romanoff J, Kitsch AE, Hanna LG, Harvey SM, Moy L, DeMartini WB, Dogan B, Yang WT, Wang LC, Joe BN, Oh KY, Neal CH, McDonald ES, Schnall MD, Lehman CD, Comstock CE, Partridge SC. Utility of Diffusion-weighted Imaging to Decrease Unnecessary Biopsies Prompted by Breast MRI: A Trial of the ECOG-ACRIN Cancer Research Group (A6702). Clin Cancer Res. 2019 Mar 15;25(6):1756-1765. doi: 10.1158/1078-0432.CCR-18-2967. Epub 2019 Jan 15.
- Lawson MB, Partridge SC, Hippe DS, Rahbar H, Lam DL, Lee CI, Lowry KP, Scheel JR, Parsian S, Li I, Biswas D, Bryant ML, Lee JM. Comparative Performance of Contrast-enhanced Mammography, Abbreviated Breast MRI, and Standard Breast MRI for Breast Cancer Screening. Radiology. 2023 Aug;308(2):e230576. doi: 10.1148/radiol.230576.
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Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования (Оцененный)
1 июня 2026 г.
Первичное завершение (Оцененный)
1 декабря 2026 г.
Завершение исследования (Оцененный)
1 мая 2027 г.
Даты регистрации исследования
Первый отправленный
12 мая 2026 г.
Впервые представлено, что соответствует критериям контроля качества
19 мая 2026 г.
Первый опубликованный (Действительный)
20 мая 2026 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
9 июня 2026 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
5 июня 2026 г.
Последняя проверка
1 мая 2026 г.
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- 2026-Ζ-52
Планирование данных отдельных участников (IPD)
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Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Нет
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .