染色变异和颜色归一化对病理学预后预测的影响

ArXiv Pub Date : 2024-09-12
Siyu Steven Lin, Haowen Zhou, Richard J Cote, Mark Watson, Ramaswamy Govindan, Changhuei Yang
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引用次数: 0

摘要

近年来,深度神经网络(DNN)在病理学应用中表现出了不俗的性能,甚至有可能超越病理专家,因为它们能够从大型数据集中学习微妙的特征。为 DNN 任务准备数字病理数据集的一个复杂问题是切面质量的变化。解决这一问题的常用方法是对图像进行染色归一化处理。在本研究中,我们发现在一批组织学切片上训练有素的 DNN 模型无法泛化到另一批在不同时间从相同组织块中制备的切片上,即使应用了染色归一化方法也是如此。本研究使用了以前报道过的 DNN 的样本数据,该 DNN 能够根据同时处理的 H&E 染色原发肿瘤组织切片的数字图像进行训练和测试,高精度地识别出肿瘤发生转移和未发生转移的早期非小细胞肺癌(NSCLC)患者。在这项研究中,我们获得了一系列新的组织切片,这些切片来自在同一实验室但在不同时间处理的相同组织块的相邻重切部分。我们发现,在其中一批切片/图像上训练的 DNN 无法泛化,也无法预测另一批切片/图像的进展(AUC_cross-batch = 0.52 - 0.53,而 AUC_same-batch = 0.74 - 0.81)。即使通过传统的颜色调整或借助循环生成对抗网络(CycleGAN)过程进行染色归一化,也无法改善无法泛化的问题。这突出表明,我们需要开发一种全新的方法来处理和收集来自组织切片的一致显微图像,这种方法既可用于训练预测性 DNN 算法,也可用于预测性 DNN 算法的普遍应用。
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Impact of Stain Variation and Color Normalization for Prognostic Predictions in Pathology.

In recent years, deep neural networks (DNNs) have demonstrated remarkable performance in pathology applications, potentially even outperforming expert pathologists due to their ability to learn subtle features from large datasets. One complication in preparing digital pathology datasets for DNN tasks is variation in tinctorial qualities. A common way to address this is to perform stain normalization on the images. In this study, we show that a well-trained DNN model trained on one batch of histological slides failed to generalize to another batch prepared at a different time from the same tissue blocks, even when stain normalization methods were applied. This study used sample data from a previously reported DNN that was able to identify patients with early stage non-small cell lung cancer (NSCLC) whose tumors did and did not metastasize, with high accuracy, based on training and then testing of digital images from H&E stained primary tumor tissue sections processed at the same time. In this study we obtained a new series of histologic slides from the adjacent recuts of same tissue blocks processed in the same lab but at a different time. We found that the DNN trained on the either batch of slides/images was unable to generalize and failed to predict progression in the other batch of slides/images (AUCcross-batch = 0.52 - 0.53 compared to AUCsame-batch = 0.74 - 0.81). The failure to generalize did not improve even when the tinctorial difference correction were made through either traditional color-tuning or stain normalization with the help of a Cycle Generative Adversarial Network (CycleGAN) process. This highlights the need to develop an entirely new way to process and collect consistent microscopy images from histologic slides that can be used to both train and allow for the general application of predictive DNN algorithms.

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