Xinyu Ma, Haotian Sun, Gang Yuan, Yufei Tang, Jie Liu, Shuangqing Chen, Jian Zheng
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引用次数: 0
摘要
数字乳腺断层摄影(DBT)中肿块的计算机辅助检测(CADe)对乳腺癌的早期诊断至关重要。然而,乳房肿块的大小和形态的可变性及其与周围组织的相似性提出了重大挑战。目前基于cnn的CADe方法,特别是使用特征金字塔网络(Feature Pyramid Networks, FPN)的方法,由于特征的单向整合和逐渐衰减,往往不能有效地整合多尺度信息,难以处理高密度或等密度肿块病变的致密腺组织,导致假阳性率高。此外,乳腺肿块的边界通常不清晰,这给边界定位带来了不确定性,使得传统的Dirac边界模型无法实现精确的边界回归。为了解决这些问题,我们提出了CU-Net网络,该网络有效地融合了多尺度特征并准确地模拟了模糊边界。具体而言,CU-Net引入了交叉注意自适应特征金字塔网络(CA-FPN),该网络通过交叉注意机制捕获多尺度特征映射的全局相关性,提高了特征交互的有效性和准确性。同时,乳房密度感知模块(Breast Density Perceptual Module, BDPM)将乳房密度信息纳入权重中间特征,从而提高网络对容易出现假阳性的致密乳房区域的关注。对于模糊的质量边界,引入不确定性边界建模(UBM)对边界不确定的质量预测边界盒的位置分布函数进行建模。在内部临床DBT数据集和BCS-DBT数据集的对比实验中,所提出的方法在每DBT体积(FPs/DBT) 2个假阳性时的灵敏度分别达到89.68%和72.73%,显著优于现有的最先进的检测方法。该方法为临床医生提供了快速、准确、客观的诊断帮助,显示了临床应用的巨大潜力。
Cross-Attention Adaptive Feature Pyramid Network with Uncertainty Boundary Modeling for Mass Detection in Digital Breast Tomosynthesis.
Computer-aided detection (CADe) of masses in digital breast tomosynthesis (DBT) is crucial for early breast cancer diagnosis. However, the variability in the size and morphology of breast masses and their resemblance to surrounding tissues present significant challenges. Current CNN-based CADe methods, particularly those that use Feature Pyramid Networks (FPN), often fail to integrate multi-scale information effectively and struggle to handle dense glandular tissue with high-density or iso-density mass lesions due to the unidirectional integration and progressive attenuation of features, leading to high false positive rates. Additionally, the commonly indistinct boundaries of breast masses introduce uncertainty in boundary localization, which makes traditional Dirac boundary modeling insufficient for precise boundary regression. To address these issues, we propose the CU-Net network, which efficiently fuses multi-scale features and accurately models blurred boundaries. Specifically, the CU-Net introduces the Cross-Attention Adaptive Feature Pyramid Network (CA-FPN), which enhances the effectiveness and accuracy of feature interactions through a cross-attention mechanism to capture global correlations across multi-scale feature maps. Simultaneously, the Breast Density Perceptual Module (BDPM) incorporates breast density information to weight intermediate features, thereby improving the network's focus on dense breast regions susceptible to false positives. For blurred mass boundaries, we introduce Uncertainty Boundary Modeling (UBM) to model the positional distribution function of predicted bounding boxes for masses with uncertain boundaries. In comparative experiments on an in-house clinical DBT dataset and the BCS-DBT dataset, the proposed method achieved sensitivities of 89.68% and 72.73% at 2 false positives per DBT volume (FPs/DBT), respectively, significantly outperforming existing state-of-the-art detection methods. This method offers clinicians rapid, accurate, and objective diagnostic assistance, demonstrating substantial potential for clinical application.
期刊介绍:
Aims
Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal:
● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings.
● Manuscripts regarding research proposals and research ideas will be particularly welcomed.
● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds.
Scope
● Bionics and biological cybernetics: implantology; bio–abio interfaces
● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices
● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc.
● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology
● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering
● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation
● Translational bioengineering