论文标题

通过决策分层检测3D肿瘤学中分散的,小且至关重要的对象

Detecting Scatteredly-Distributed, Small, andCritically Important Objects in 3D OncologyImaging via Decision Stratification

论文作者

Zhu, Zhuotun, Yan, Ke, Jin, Dakai, Cai, Jinzheng, Ho, Tsung-Ying, Harrison, Adam P, Guo, Dazhou, Chao, Chun-Hung, Ye, Xianghua, Xiao, Jing, Yuille, Alan, Lu, Le

论文摘要

在3D肿瘤学图像中查找和识别分散分散,小且至关重要的对象非常具有挑战性。我们专注于肿瘤学 - 重要(或可疑癌症转移)淋巴结(OSLNS)的检测和分割,在以前尚未将其作为计算任务进行研究。确定和描述OSLN的扩散对于定义相应的切除/辐照区域对于手术切除和各种癌症的放射疗法的下游工作流程至关重要。对于接受放射疗法治疗的患者,这项任务是由经验丰富的放射肿瘤学家执行的,涉及有关LNS是否被转移的高级推理,这可能会受到高观察者间变异的影响。在这项工作中,我们提出了一种分裂和纠缠的决策分层方法,该方法将OSLN分为肿瘤 - 抗肿瘤和肿瘤距离类别。这是由于观察到每个类别在外观,大小和其他特征上具有不同的潜在分布的动机。每个类别训练并融合了两个单独的逐段检测网络。为了进一步降低假阳性(FP),我们提出了一种新型的全球本地网络(GLNET),该网络将高级病变特征与从局部3D图像贴片中学到的特征相结合。我们的方法在141名具有PET和CT模式的食管癌患者的数据集上进行了评估(最大的迄今为止)。与以前的最新方法相比,我们的结果将从$ 45 \%$ $ $ $ $ $ 3 $ fps $ 3 $ fps提高到67美元。达到0.828美元的OSLN召回率最高的是临床相关且有价值的。

Finding and identifying scatteredly-distributed, small, and critically important objects in 3D oncology images is very challenging. We focus on the detection and segmentation of oncology-significant (or suspicious cancer metastasized) lymph nodes (OSLNs), which has not been studied before as a computational task. Determining and delineating the spread of OSLNs is essential in defining the corresponding resection/irradiating regions for the downstream workflows of surgical resection and radiotherapy of various cancers. For patients who are treated with radiotherapy, this task is performed by experienced radiation oncologists that involves high-level reasoning on whether LNs are metastasized, which is subject to high inter-observer variations. In this work, we propose a divide-and-conquer decision stratification approach that divides OSLNs into tumor-proximal and tumor-distal categories. This is motivated by the observation that each category has its own different underlying distributions in appearance, size and other characteristics. Two separate detection-by-segmentation networks are trained per category and fused. To further reduce false positives (FP), we present a novel global-local network (GLNet) that combines high-level lesion characteristics with features learned from localized 3D image patches. Our method is evaluated on a dataset of 141 esophageal cancer patients with PET and CT modalities (the largest to-date). Our results significantly improve the recall from $45\%$ to $67\%$ at $3$ FPs per patient as compared to previous state-of-the-art methods. The highest achieved OSLN recall of $0.828$ is clinically relevant and valuable.

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