Identifying primary tumor site of origin for liver metastases via a combination of handcrafted and deep learning features

IF 3.4 2区 医学 Q1 PATHOLOGY
Chuheng Chen, Cheng Lu, Vidya Viswanathan, Brandon Maveal, Bhunesh Maheshwari, Joseph Willis, Anant Madabhushi
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引用次数: 0

Abstract

Liver is one of the most common sites for metastases, which can occur on account of primary tumors from multiple sites of origin. Identifying the primary site of origin (PSO) of a metastasis can help in guiding therapeutic options for liver metastases. In this pilot study, we hypothesized that computer extracted handcrafted (HC) histomorphometric features can be utilized to identify the PSO of liver metastases. Cellular features, including tumor nuclei morphological and graph features as well as cytoplasm texture features, were extracted by computer algorithms from 175 slides (114 patients). The study comprised three experiments: (1) comparing and (2) fusing a machine learning (ML) model trained with HC pathomic features and deep learning (DL)-based classifiers to predict site of origin; (3) identifying the section of the primary tumor from which metastases were derived. For experiment 1, we divided the cohort into training sets composed of primary and matched liver metastases [60 patients, 121 whole slide images (WSIs)], and a hold-out validation set (54 patients, 54 WSIs) composed solely of liver metastases of known site of origin. Using the extracted HC features of the training set, a combination of supervised machine classifiers and unsupervised clustering was applied to identify the PSO. A random forest classifier achieved areas under the curve (AUCs) of 0.83, 0.64, 0.82, and 0.64 in classifying the metastatic tumor from colon, esophagus, breast, and pancreas on the validation set. The top features related to nuclear and peri-nuclear shape and textural attributes. We also trained a DL network to serve as a direct comparison to our method. The DL model achieved AUCs for colon: 0.94, esophagus: 0.66, breast: 0.79, and pancreas: 0.67 in identifying PSO. A decision fusion-based strategy was deployed to fuse the trained ML and DL classifiers and achieved slightly better results than ML or DL classifier alone (colon: 0.93, esophagus: 0.68, breast: 0.81, and pancreas: 0.69). For the third experiment, WSI-level attention maps were also generated using a trained DL network to generate a composite feature similarity heat map between paired primaries and their associated metastases. Our experiments revealed that epithelium-rich and moderately differentiated tumor regions of primary tumors were quantitatively similar to paired metastatic tumors. Our findings suggest that a combination of HC and DL features could potentially help identify the PSO for liver metastases while at the same time also potentially identify the spatial sites of origin for the metastases within primary tumors.

Abstract Image

通过手工制作和深度学习特征相结合来识别肝转移的原发性肿瘤起源部位。
肝脏是最常见的转移部位之一,由于多个来源的原发性肿瘤,可能会发生转移。确定转移的原发灶(PSO)有助于指导肝转移的治疗选择。在这项初步研究中,我们假设计算机提取的手工(HC)组织形态计量学特征可以用于识别肝转移的PSO。通过计算机算法从175张幻灯片(114名患者)中提取细胞特征,包括肿瘤细胞核形态和图形特征以及细胞质纹理特征。该研究包括三个实验:(1)比较和(2)融合用HC病理特征训练的机器学习(ML)模型和基于深度学习(DL)的分类器来预测起源地;(3) 鉴定转移瘤来源的原发性肿瘤的切片。对于实验1,我们将队列分为由原发性和匹配的肝转移组成的训练集[60名患者,121张全玻片图像(WSI)]和仅由已知起源部位的肝转移构成的保留验证集(54名患者,54张WSI)。利用提取的训练集HC特征,将有监督机器分类器和无监督聚类相结合来识别PSO。随机森林分类器在对验证集上来自结肠、食道、乳腺和胰腺的转移性肿瘤进行分类时,获得了0.83、0.64、0.82和0.64的曲线下面积(AUCs)。顶部特征与核和核周围的形状和质地属性有关。我们还训练了一个DL网络,作为与我们的方法的直接比较。DL模型在鉴定PSO时实现了结肠的AUCs:0.94,食道的AUCs为0.66,乳腺的AUCs是0.79,胰腺的AUCs也是0.67。部署了一种基于决策融合的策略来融合训练的ML和DL分类器,并取得了比单独的ML或DL分类器略好的结果(结肠:0.93,食道:0.68,乳房:0.81,胰腺:0.69)。对于第三个实验,还使用训练的DL网络生成WSI级注意力图,以生成配对原发性肿瘤及其相关转移之间的复合特征相似性热图。我们的实验表明,原发性肿瘤的富含上皮和中等分化的肿瘤区域在数量上与成对的转移性肿瘤相似。我们的研究结果表明,HC和DL特征的结合可能有助于识别肝转移的PSO,同时也可能识别原发性肿瘤内转移的空间起源位点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pathology Clinical Research
Journal of Pathology Clinical Research Medicine-Pathology and Forensic Medicine
CiteScore
7.40
自引率
2.40%
发文量
47
审稿时长
20 weeks
期刊介绍: The Journal of Pathology: Clinical Research and The Journal of Pathology serve as translational bridges between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The focus of The Journal of Pathology: Clinical Research is the publication of studies that illuminate the clinical relevance of research in the broad area of the study of disease. Appropriately powered and validated studies with novel diagnostic, prognostic and predictive significance, and biomarker discover and validation, will be welcomed. Studies with a predominantly mechanistic basis will be more appropriate for the companion Journal of Pathology.
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