Detection of abdominopelvic lymph nodes in multi-parametric MRI

IF 5.4 2区 医学 Q1 ENGINEERING, BIOMEDICAL
Tejas Sudharshan Mathai , Thomas C. Shen , Daniel C. Elton , Sungwon Lee , Zhiyong Lu , Ronald M. Summers
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引用次数: 0

Abstract

Reliable localization of lymph nodes (LNs) in multi-parametric MRI (mpMRI) studies plays a major role in the assessment of lymphadenopathy and staging of metastatic disease. Radiologists routinely measure the nodal size in order to distinguish benign from malignant nodes, which require subsequent cancer staging. However, identification of lymph nodes is a cumbersome task due to their myriad appearances in mpMRI studies. Multiple sequences are acquired in mpMRI studies, including T2 fat suppressed (T2FS) and diffusion weighted imaging (DWI) sequences among others; consequently, the sizing of LNs is rendered challenging due to the variety of signal intensities in these sequences. Furthermore, radiologists can miss potentially metastatic LNs during a busy clinical day. To lighten these imaging and workflow challenges, we propose a computer-aided detection (CAD) pipeline to detect both benign and malignant LNs in the body for their subsequent measurement. We employed the recently proposed Dynamic Head (DyHead) neural network to detect LNs in mpMRI studies that were acquired using a variety of scanners and exam protocols. The T2FS and DWI series were co-registered, and a selective augmentation technique called Intra-Label LISA (ILL) was used to blend the two volumes with the interpolation factor drawn from a Beta distribution. In this way, ILL diversified the samples that the model encountered during the training phase, while the requirement for both sequences to be present at test time was nullified. Our results showed a mean average precision (mAP) of 53.5% and a sensitivity of 78% with ILL at 4 FP/vol. This corresponded to an improvement of 10% in mAP and 12% in sensitivity at 4FP (p ¡ 0.05) respectively over current LN detection approaches evaluated on the same dataset. We also established the out-of-distribution robustness of the DyHead model by training it on data acquired by a Siemens Aera scanner and testing it on data from the Siemens Verio, Siemens Biograph mMR, and Philips Achieva scanners. Our pilot work represents an important first step towards automated detection, segmentation, and classification of lymph nodes in mpMRI.

在多参数磁共振成像中检测腹盆腔淋巴结
多参数磁共振成像(mpMRI)研究中淋巴结(LN)的可靠定位在淋巴结病的评估和转移性疾病的分期中起着重要作用。放射科医生通常会测量淋巴结的大小,以区分良性和恶性淋巴结,这需要随后进行癌症分期。然而,由于淋巴结在 mpMRI 研究中的表现多种多样,淋巴结的识别是一项繁琐的工作。在 mpMRI 研究中会采集多个序列,包括 T2 脂肪抑制(T2FS)和弥散加权成像(DWI)序列等;因此,由于这些序列中信号强度的多样性,确定淋巴结的大小就变得非常具有挑战性。此外,放射科医生可能会在繁忙的临床工作中错过潜在的转移性 LN。为了减轻这些成像和工作流程方面的挑战,我们提出了一种计算机辅助检测(CAD)管道,用于检测体内良性和恶性 LN,以便进行后续测量。我们采用了最近提出的动态头部(DyHead)神经网络来检测使用各种扫描仪和检查方案获得的 mpMRI 研究中的 LN。对 T2FS 和 DWI 序列进行共同注册,并使用一种称为标签内 LISA(ILL)的选择性增强技术,利用从 Beta 分布中提取的插值因子混合两个体量。通过这种方式,ILL 使模型在训练阶段遇到的样本多样化,同时取消了测试时两个序列同时存在的要求。结果表明,在 4 FP/vol 的条件下,ILL 的平均精确度(mAP)为 53.5%,灵敏度为 78%。与目前在相同数据集上评估的 LN 检测方法相比,4FP 的 mAP 和灵敏度分别提高了≥10% 和≥12%(p ¡ 0.05)。我们还在西门子Aera扫描仪获取的数据上对DyHead模型进行了训练,并在西门子Verio、西门子Biograph mMR和飞利浦Achieva扫描仪的数据上进行了测试,从而确定了DyHead模型在分布外的鲁棒性。我们的试验性工作代表着向 mpMRI 中淋巴结的自动检测、分割和分类迈出了重要的第一步。
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来源期刊
CiteScore
10.70
自引率
3.50%
发文量
71
审稿时长
26 days
期刊介绍: The purpose of the journal Computerized Medical Imaging and Graphics is to act as a source for the exchange of research results concerning algorithmic advances, development, and application of digital imaging in disease detection, diagnosis, intervention, prevention, precision medicine, and population health. Included in the journal will be articles on novel computerized imaging or visualization techniques, including artificial intelligence and machine learning, augmented reality for surgical planning and guidance, big biomedical data visualization, computer-aided diagnosis, computerized-robotic surgery, image-guided therapy, imaging scanning and reconstruction, mobile and tele-imaging, radiomics, and imaging integration and modeling with other information relevant to digital health. The types of biomedical imaging include: magnetic resonance, computed tomography, ultrasound, nuclear medicine, X-ray, microwave, optical and multi-photon microscopy, video and sensory imaging, and the convergence of biomedical images with other non-imaging datasets.
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