- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07743749
An MRI-Based Study of Intelligent Pathological Subtyping and Grading of Renal Tumors
Обзор исследования
Статус
Вмешательство/лечение
Подробное описание
Renal tumors include multiple benign and malignant pathological subtypes with substantial differences in biological behavior, treatment strategy, and prognosis. Surgical planning and clinical management are closely related to the pathological subtype and histological grade of the tumor. However, accurately determining these pathological characteristics before surgery using conventional MRI interpretation remains challenging.
This is a retrospective + prospective, observational, and non-interventional study. Adult patients with renal tumors will be identified from existing clinical records. Eligible patients will have available renal MRI examinations and corresponding pathological diagnoses, including pathological subtype and, when applicable, histological grade. Cases with unreadable MRI data or images of insufficient quality for analysis will be excluded.
Existing study data will include multisequence MRI examinations, such as T1-weighted imaging, T2-weighted imaging, diffusion-weighted imaging, apparent diffusion coefficient imaging, fat-suppressed imaging, and contrast-enhanced imaging, when available. Demographic information, relevant clinical history, laboratory results, and radiology report information may also be collected. Pathological findings will serve as the reference standard for model training and evaluation. All data will be de-identified before processing and analysis.
The study will develop artificial intelligence models for the following tasks:
- Detection and localization of renal tumors on multisequence MRI.
- Segmentation of renal tumors and extraction of quantitative imaging features.
- Classification of common benign and malignant renal tumor subtypes.
- Identification of rare pathological subtypes using small-sample or cross-modal learning methods.
- Prediction of histological grade for malignant renal tumors.
- Integration of MRI, demographic, clinical, and laboratory information to improve pathological subtyping and grading.
The dataset will be divided into model-development and validation datasets. Additional cases collected from different time periods or participating sources may be used for independent testing. Model performance will be evaluated by comparing artificial intelligence predictions with pathological diagnoses.
This study does not assign any treatment or diagnostic intervention. It will not affect participants' routine clinical care and will not require additional imaging examinations, blood collection, surgery, medication, or follow-up visits. The study is intended to develop an intelligent MRI-based diagnostic system that may support preoperative decision-making for patients with renal tumors.
Тип исследования
Регистрация (Оцененный)
Контакты и местонахождение
Контакты исследования
- Имя: Xiongjun Ye
- Номер телефона: 010-87787170 010-87787170
- Электронная почта: yexiongjun@cicams.ac.cn
Места учебы
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Beijing, Китай
- Рекрутинг
- Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College
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Контакт:
- xiongjun YE
- Номер телефона: 010-87787170
- Электронная почта: yexiongjun@cicams.ac.cn
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
- Пожилой взрослый
Принимает здоровых добровольцев
Метод выборки
Исследуемая популяция
Описание
Inclusion Criteria:
- Patients aged 18 years or older.
- Patients diagnosed with a renal tumor.
- Availability of preoperative renal magnetic resonance imaging examinations.
- Availability of a corresponding pathological diagnosis, including pathological subtype and, where applicable, histological grade.
- Magnetic resonance images that can be successfully retrieved and are of - - sufficient quality for image analysis.
Exclusion Criteria:
- Absence of renal magnetic resonance imaging data.
- Absence of a corresponding pathological diagnosis or insufficient pathological subtype or grading information.
- Magnetic resonance images that cannot be retrieved, opened, or read.
- Poor image quality that precludes reliable image annotation or artificial intelligence analysis.
Учебный план
Как устроено исследование?
Детали дизайна
Когорты и вмешательства
Группа / когорта |
Вмешательство/лечение |
|---|---|
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Patients With Renal Tumors
Adult patients with pathologically confirmed renal tumors who underwent preoperative multisequence renal MRI as part of routine clinical care and had available pathological subtype and, when applicable, histological grade information.
Existing de-identified MRI, pathological, clinical, and laboratory data were collected for artificial intelligence model development and evaluation.
No additional examination, treatment, or study-specific intervention was administered.
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Existing preoperative multisequence renal MRI images, including T1-weighted imaging, T2-weighted imaging, diffusion-weighted imaging, apparent diffusion coefficient imaging, fat-suppressed imaging, and contrast-enhanced imaging when available, were retrospectively analyzed using artificial intelligence and deep learning methods.
The models were developed to detect and segment renal tumors and to predict pathological subtype and histological grade.
Postoperative pathological findings were used as the reference standard.
No additional MRI examination or diagnostic procedure was performed for the study.
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Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Accuracy of MRI-Based Artificial Intelligence for Pathological Subtyping of Renal Tumors
Временное ограничение: At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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The pathological subtype predicted by the MRI-based artificial intelligence model will be compared with the postoperative pathological diagnosis as the reference standard in the held-out test dataset.
Accuracy will be calculated as the number of correctly classified renal tumors divided by the total number of renal tumors evaluated.
Classification performance for individual pathological subtypes will also be summarized using sensitivity, specificity, and F1 score, where applicable.
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At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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Accuracy of MRI-Based Artificial Intelligence for Histological Grading of Malignant Renal Tumors
Временное ограничение: At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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The histological grade predicted by the MRI-based artificial intelligence model will be compared with the postoperative pathological grade as the reference standard.
Histological grading will be assessed according to the four-tier World Health Organization/International Society of Urological Pathology grading system.
Accuracy will be calculated as the number of malignant renal tumors with correctly predicted histological grade divided by the total number of malignant renal tumors evaluated.
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At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
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Performance of the Artificial Intelligence Model for Renal Tumor Detection
Временное ограничение: At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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The ability of the artificial intelligence model to detect and localize renal tumors on multisequence MRI will be evaluated by comparing model-generated tumor locations with expert manual annotations.
Detection performance will be summarized using sensitivity and the proportion of correctly localized renal tumors.
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At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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Accuracy of Artificial Intelligence-Based Renal Tumor Segmentation
Временное ограничение: At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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Artificial intelligence-generated renal tumor segmentations will be compared with pixel-level manual annotations prepared under the supervision of experienced physicians.
Segmentation agreement will be evaluated using the Dice similarity coefficient.
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At completion of model evaluation using retrospective data collected from January 2021 through July 2026 and prospective data collected through December 2026.
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Соавторы и исследователи
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Оцененный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
- Урогенитальные заболевания
- Урогенитальные новообразования
- Новообразования по локализации
- Новообразования
- Мужские мочеполовые заболевания
- Заболевания почек
- Урологические заболевания
- Женские урогенитальные заболевания
- Женские мочеполовые заболевания и осложнения беременности
- Новообразования по гистологическому типу
- Новообразования железистые и эпителиальные
- Аденокарцинома
- Урологические новообразования
- Карцинома
- Карцинома, почечно-клеточная
- Новообразования почек
Другие идентификационные номера исследования
- NCC-020738
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
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