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NCT Number: NCT07500428

Construction of a Benchmark for Breast Ultrasound AI Interpretation and Performance Evaluation of Multimodal AI Models

This single-center, retrospective, observational study aims to construct a standardized benchmark evaluation system for intelligent breast ultrasound image interpretation and to systematically assess the diagnostic performance of current mainstream multimodal artificial intelligence (AI) models.

De-identified B-mode breast ultrasound images with confirmed pathological diagnoses will be retrospectively collected from the institutional archive (2018-2025) and supplemented with images from published open-access datasets. Expert radiologists with varying experience levels will independently annotate all images according to the American College of Radiology (ACR) Breast Imaging Reporting and Data System (BI-RADS) v2025 criteria, including glandular tissue composition, lesion characterization (mass vs. non-mass lesion), morphological descriptors, and final BI-RADS classification.

Baseline deep learning models (CNN-based ResNet-50 and Transformer-based USFM) will be trained to establish performance baselines and to stratify cases by diagnostic difficulty through cross-architecture consensus. Multiple multimodal large language models (MLLMs), including both general-purpose and medical-domain models, will then be evaluated via standardized API calls using BI-RADS-guided chain-of-thought prompts at temperature 0 for reproducibility.

Primary endpoints include BI-RADS classification accuracy and diagnostic AUC for benign-malignant differentiation. Model robustness and safety will be assessed through out-of-distribution rejection testing, temperature-stability experiments, and thinking-mode ablation studies. This study adheres to the FLAIR and TRIPOD-LLM reporting guidelines.

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Key information

Age range

18 year–75 year

Sex eligibility

Female

Study type

Observational

Primary location

Peking Union Medical College Hospital

Beijing, 100730, China

Location status: Recruiting

Location contact

Qingli Zhu, MD

CONTACT

[email protected]

+86 13621376699

About this study

Background: Breast cancer is the most prevalent malignancy among women worldwide. Ultrasound is a first-line screening modality, particularly in Asian populations with dense breast tissue where mammographic sensitivity is limited. However, ultrasound interpretation is highly operator-dependent, with substantial inter-observer variability in BI-RADS classification, especially for category 4A-4B lesions. Multimodal large language models (MLLMs) have emerged as a promising tool for medical image analysis due to their zero-shot diagnostic capability, interpretable chain-of-thought reasoning, and structured report generation. Nevertheless, there is currently no standardized benchmark for evaluating AI performance in breast ultrasound interpretation.

Study Design: Approximately 1,380 breast ultrasound images will be curated (1,200 evaluation set + 150 out-of-distribution safety test set + 30 prompt development set), encompassing three diagnostic categories: normal breast, benign lesions (BI-RADS 2-4B), and malignant lesions (BI-RADS 3-5). Two junior radiologists (<5 years of experience) and two senior radiologists (>15 years) will independently annotate images per ACR BI-RADS v2025 with arbitration by a fifth expert for discordant cases.

Diagnostic difficulty will be stratified into three tiers using cross-architecture deep learning consensus: Tier 1 (straightforward, both models correct), Tier 2 (equivocal, one correct/one incorrect), and Tier 3 (difficult, both incorrect, with senior expert validation). MLLMs will be evaluated across multiple dimensions: classification accuracy, sensitivity, specificity, F1 score, AUC, Cohen's kappa agreement with expert consensus, expected calibration error (ECE), morphological feature description accuracy, and chain-of-thought reasoning quality.

Safety Assessment: (1) Out-of-distribution rejection test using 150 non-diagnostic images (degraded images, non-breast ultrasound, other imaging modalities); (2) Temperature-stability pre-experiment across parameter settings; (3) Thinking-mode ablation comparing standard vs. chain-of-thought reasoning modes. All experiments use fixed model snapshots, system fingerprint monitoring, and complete logging for reproducibility.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • B-mode breast ultrasound grayscale images from the institutional PACS database or from published open-access breast ultrasound datasets with documented original institutional ethics approval
  • Image quality adequate for clinical diagnosis with clear visualization of the region of interest
  • Pathological diagnosis confirmed (for benign and malignant lesion groups), or normal breast status confirmed by a senior radiologist with >15 years of breast ultrasound experience (for the normal group)
  • Complete de-identification with removal of all personally identifiable information

Exclusion criteria

  • Severely degraded image quality precluding meaningful BI-RADS assessment
  • Duplicate images from the same patient (only the most representative image retained per lesion)
  • Images with residual personally identifiable information after de-identification processing
  • Cases with ambiguous, disputed, or unavailable pathological results
  • Non-B-mode ultrasound images, including elastography, contrast-enhanced ultrasound, and Doppler imaging

Treatment and study plan

Multimodal AI Model Diagnostic Evaluation

Diagnostic Test

Retrospective evaluation of de-identified breast ultrasound images by multiple AI systems, including baseline deep learning models (ResNet-50, USFM) and multimodal large language models, using standardized BI-RADS-guided chain-of-thought prompts via API. No patient contact or clinical decision-making is involved.

Primary outcomes

  1. Diagnostic Accuracy for Pathological Diagnosis

    Time frame: At study completion, approximately 12 months

    Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and F1 score of AI models for benign-malignant classification, with histopathological diagnosis as the gold standard.

  2. BI-RADS Classification Accuracy

    Time frame: At study completion, approximately 12 months

    Overall accuracy of AI models in assigning BI-RADS categories (2, 3, 4A, 4B, 4C, 5) to breast ultrasound images, compared with expert consensus annotation as the reference standard.

Secondary outcomes

  1. Agreement with Expert Consensus (Cohen's Kappa)

    Time frame: At study completion, approximately 12 months

    Cohen's kappa coefficient measuring agreement between each AI model's BI-RADS classification and the expert consensus annotation, reported with 95% confidence intervals.

  2. Out-of-Distribution Rejection Rate

    Time frame: At study completion, approximately 12 months

    Proportion of non-diagnostic images (degraded quality, non-breast ultrasound, other imaging modalities) correctly identified and refused by AI models, evaluating domain safety.

  3. Sensitivity, Specificity, PPV, NPV, and F1 Score

    Time frame: At study completion, approximately 12 months

    Standard diagnostic performance metrics for benign-malignant classification, reported for each AI model individually.

Study contacts

Contact information is provided by the study sponsor or research team.

Qingli Zhu, MD

CONTACT

[email protected]

+86 13621376699

Yinglan Wu, MD

CONTACT

[email protected]

+86 15626121076

Sponsors and collaborators

Lead sponsor

Peking Union Medical College Hospital

Other

Collaborators

  • Chinese Academy of Medical Sciences

Registry information

Official study title

Construction of a Standardized Benchmark Evaluation System for Intelligent Breast Ultrasound Image Interpretation and Systematic Performance Assessment of Multimodal Artificial Intelligence Models Based on ACR BI-RADS v2025 Criteria

Acronym: BUST-AI Bench

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Mar 30, 2026
Registry last updated
Mar 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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