4.7 Article

Weakly Supervised Deep Ordinal Cox Model for Survival Prediction From Whole-Slide Pathological Images

期刊

IEEE TRANSACTIONS ON MEDICAL IMAGING
卷 40, 期 12, 页码 3739-3747

出版社

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TMI.2021.3097319

关键词

Predictive models; Cancer; Computational modeling; Prognostics and health management; Tumors; Hazards; Analytical models; Histopathological images; weakly supervised learning; survival analysis; ordinal cox model

资金

  1. Indiana University Precision Health Initiative

向作者/读者索取更多资源

WSI is considered as the gold standard for cancer diagnosis and prognosis. However, existing prediction models do not efficiently utilize ordinal information among patients, and the large size and single label of WSIs complicate the training process.
Whole-Slide Histopathology Image (WSI) is generally considered the gold standard for cancer diagnosis and prognosis. Given the large inter-operator variation among pathologists, there is an imperative need to develop machine learning models based on WSIs for consistently predicting patient prognosis. The existing WSI-based prediction methods do not utilize the ordinal ranking loss to train the prognosis model, and thus cannot model the strong ordinal information among different patients in an efficient way. Another challenge is that a WSI is of large size (e.g., 100,000-by-100,000 pixels) with heterogeneous patterns but often only annotated with a single WSI-level label, which further complicates the training process. To address these challenges, we consider the ordinal characteristic of the survival process by adding a ranking-based regularization term on the Cox model and propose a weakly supervised deep ordinal Cox model (BDOCOX) for survival prediction from WSIs. Here, we generate amounts of bags from WSIs, and each bag is comprised of the image patches representing the heterogeneous patterns of WSIs, which is assumed to match the WSI-level labels for training the proposed model. The effectiveness of the proposed method is well validated by theoretical analysis as well as the prognosis and patient stratification results on three cancer datasets from The Cancer Genome Atlas (TCGA).

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