PLoS Medicine · 2019 · 1.1K citations · 41 references
ComputingComputer ScienceOncologyComputer VisionGastrointestinal OncologyMachine LearningCancer StagingColorectal CancerDeep LearningMedical Image AnalysisTumor ClassificationTumor HistopathologyColorectal Cancer BiomarkersColorectal Cancer PathologyConvolutional Neural NetworksDigital Pathology AnalysisDisease Prognostic BiomarkersHistopathological InterpretationPrognostic BiomarkersPrognostic Models
HE‑stained colorectal cancer slides are widely available and contain quantitative information that is not routinely used for prognostic biomarkers, and prospective validation is needed before clinical implementation. The study investigates whether deep convolutional neural networks can extract prognostic biomarkers directly from routine HE‑stained.
Background For virtually every patient with colorectal cancer (CRC), hematoxylin–eosin (HE)–stained tissue slides are available. These images contain quantitative information, which is not routinely used to objectively extract prognostic biomarkers. In the present study, we investigated whether deep convolutional neural networks (CNNs) can extract prognosticators directly from these widely available images. Methods and findings We hand-delineated single-tissue regions in 86 CRC tissue slides, yielding more than 100,000 HE image patches, and used these to train a CNN by transfer learning, reaching a nine-class accuracy of >94% in an independent data set of 7,180 images from 25 CRC patients. With this tool, we performed automated tissue decomposition of representative multitissue HE images from 862 HE slides in 500 stage I–IV CRC patients in the The Cancer Genome Atlas (TCGA) cohort, a large international multicenter collection of CRC tissue. Based on the output neuron activations in the CNN, we calculated a "deep stroma score," which was an independent prognostic factor for overall survival (OS) in a multivariable Cox proportional hazard model (hazard ratio [HR] with 95% confidence interval [CI]: 1.99 [1.27–3.12], p = 0.0028), while in the same cohort, manual quantification of stromal areas and a gene expression signature of cancer-associated fibroblasts (CAFs) were only prognostic in specific tumor stages. We validated these findings in an independent cohort of 409 stage I–IV CRC patients from the "Darmkrebs: Chancen der Verhütung durch Screening" (DACHS) study who were recruited between 2003 and 2007 in multiple institutions in Germany. Again, the score was an independent prognostic factor for OS (HR 1.63 [1.14–2.33], p = 0.008), CRC-specific OS (HR 2.29 [1.5–3.48], p = 0.0004), and relapse-free survival (RFS; HR 1.92 [1.34–2.76], p = 0.0004). A prospective validation is required before this biomarker can be implemented in clinical workflows. Conclusions In our retrospective study, we show that a CNN can assess the human tumor microenvironment and predict prognosis directly from histopathological images.
41
Deep Residual Learning for Image Recognition
Kaiming He, Xiangyu Zhang, Shaoqing Ren et al. · 2016 · 222.1K citations · Full text
Going deeper with convolutions
Christian Szegedy, Wei Liu, Yangqing Jia et al. · 2015 · 46.8K citations
Laurens van der Maaten, Geoffrey E. Hinton · Journal of Machine Learning Research · 2008 · 35.7K citations
Mastering the game of Go with deep neural networks and tree search
David Silver, Aja Huang, Chris J. Maddison et al. · Nature · 2016 · 15.8K citations