Mischa de Ridder

Prerak Mody, Nicolas F. Chaves-de-Plaza, Chinmay Rao et al.

Increased usage of automated tools like deep learning in medical image segmentation has alleviated the bottleneck of manual contouring. This has shifted manual labour to quality assessment (QA) of automated contours which involves detecting errors and correcting them. A potential solution to semi-automated QA is to use deep Bayesian uncertainty to recommend potentially erroneous regions, thus reducing time spent on error detection. Previous work has investigated the correspondence between uncertainty and error, however, no work has been done on improving the "utility" of Bayesian uncertainty maps such that it is only present in inaccurate regions and not in the accurate ones. Our work trains the FlipOut model with the Accuracy-vs-Uncertainty (AvU) loss which promotes uncertainty to be present only in inaccurate regions. We apply this method on datasets of two radiotherapy body sites, c.f. head-and-neck CT and prostate MR scans. Uncertainty heatmaps (i.e. predictive entropy) are evaluated against voxel inaccuracies using Receiver Operating Characteristic (ROC) and Precision-Recall (PR) curves. Numerical results show that when compared to the Bayesian baseline the proposed method successfully suppresses uncertainty for accurate voxels, with similar presence of uncertainty for inaccurate voxels. Code to reproduce experiments is available at https://github.com/prerakmody/bayesuncertainty-error-correspondence

E. M. C. Sijben, J. C. Jansen, M. de Ridder et al.

Volume measurement of a paraganglioma (a rare neuroendocrine tumor that typically forms along major blood vessels and nerve pathways in the head and neck region) is crucial for monitoring and modeling tumor growth in the long term. However, in clinical practice, using available tools to do these measurements is time-consuming and suffers from tumor-shape assumptions and observer-to-observer variation. Growth modeling could play a significant role in solving a decades-old dilemma (stemming from uncertainty regarding how the tumor will develop over time). By giving paraganglioma patients treatment, severe symptoms can be prevented. However, treating patients who do not actually need it, comes at the cost of unnecessary possible side effects and complications. Improved measurement techniques could enable growth model studies with a large amount of tumor volume data, possibly giving valuable insights into how these tumors develop over time. Therefore, we propose an automated tumor volume measurement method based on a deep learning segmentation model using no-new-UNnet (nnUNet). We assess the performance of the model based on visual inspection by a senior otorhinolaryngologist and several quantitative metrics by comparing model outputs with manual delineations, including a comparison with variation in manual delineation by multiple observers. Our findings indicate that the automatic method performs (at least) equal to manual delineation. Finally, using the created model, and a linking procedure that we propose to track the tumor over time, we show how additional volume measurements affect the fit of known growth functions.