DeepScope: Nonintrusive Whole Slide Saliency Annotation and Prediction from Pathologists at the Microscope.

Andrew J Schaumberg, S Joseph Sirintrapun, Hikmat A Al-Ahmadie, Peter J Schüffler, Thomas J Fuchs
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Abstract

Modern digital pathology departments have grown to produce whole-slide image data at petabyte scale, an unprecedented treasure chest for medical machine learning tasks. Unfortunately, most digital slides are not annotated at the image level, hindering large-scale application of supervised learning. Manual labeling is prohibitive, requiring pathologists with decades of training and outstanding clinical service responsibilities. This problem is further aggravated by the United States Food and Drug Administration's ruling that primary diagnosis must come from a glass slide rather than a digital image. We present the first end-to-end framework to overcome this problem, gathering annotations in a nonintrusive manner during a pathologist's routine clinical work: (i) microscope-specific 3D-printed commodity camera mounts are used to video record the glass-slide-based clinical diagnosis process; (ii) after routine scanning of the whole slide, the video frames are registered to the digital slide; (iii) motion and observation time are estimated to generate a spatial and temporal saliency map of the whole slide. Demonstrating the utility of these annotations, we train a convolutional neural network that detects diagnosis-relevant salient regions, then report accuracy of 85.15% in bladder and 91.40% in prostate, with 75.00% accuracy when training on prostate but predicting in bladder, despite different pathologists examining the different tissues. When training on one patient but testing on another, AUROC in bladder is 0.79±0.11 and in prostate is 0.96±0.04. Our tool is available at https://bitbucket.org/aschaumberg/deepscope.

Abstract Image

Abstract Image

Abstract Image

DeepScope:来自显微镜下病理学家的非侵入式全切片 Saliency 注释和预测。
现代数字病理部门已发展到能产生 PB 级规模的全切片图像数据,这是医学机器学习任务前所未有的宝库。遗憾的是,大多数数字切片并没有在图像层面上进行标注,这阻碍了监督学习的大规模应用。人工标注的难度很大,需要病理学家接受数十年的培训并承担出色的临床服务责任。美国食品和药物管理局规定,主要诊断必须来自玻璃载玻片而非数字图像,这进一步加剧了这一问题。我们提出了首个端到端框架来克服这一问题,在病理学家的常规临床工作中以非侵入方式收集注释:(i) 使用显微镜专用的 3D 打印商品相机支架来视频记录基于玻璃载玻片的临床诊断过程;(ii) 在对整个载玻片进行常规扫描后,将视频帧注册到数字载玻片上;(iii) 对运动和观察时间进行估计,以生成整个载玻片的空间和时间显著性地图。为了证明这些注释的实用性,我们训练了一个卷积神经网络来检测与诊断相关的突出区域,结果表明,尽管不同的病理学家检查了不同的组织,但对膀胱和前列腺的准确率分别为 85.15%和 91.40%,其中对前列腺进行训练而对膀胱进行预测的准确率为 75.00%。在对一名患者进行训练而对另一名患者进行测试时,膀胱的 AUROC 为 0.79±0.11,前列腺的 AUROC 为 0.96±0.04。我们的工具见 https://bitbucket.org/aschaumberg/deepscope。
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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