ULS+: Data-driven Model Adaptation Enhances Lesion Segmentation
Rianne Weber, Niels Rocholl, Max de Grauw, Mathias Prokop, Ewoud Smit, Alessa Hering
TL;DR
ULS+ enhances interactive whole-body lesion segmentation by integrating six additional fully annotated public datasets and introducing click-point augmentation, paired with a reduced input size to accelerate inference. The method improves Dice similarity and robustness to click-point variations over the original ULS baseline, achieving first place on the ULS23 leaderboard and enabling faster, clinically tractable inference (~0.5 s on an A100 with TTA). Key innovations include data-driven expansion of training data, lesion-shifting augmentation, and test-time augmentation, all implemented within nnUNet v2 on $128 \times 128 \times 64$ inputs. The work demonstrates that continual, data-centered updates can yield robust, scalable improvements for longitudinal lesion quantification, with reproducible code available to support adoption and further development.
Abstract
In this study, we present ULS+, an enhanced version of the Universal Lesion Segmentation (ULS) model. The original ULS model segments lesions across the whole body in CT scans given volumes of interest (VOIs) centered around a click-point. Since its release, several new public datasets have become available that can further improve model performance. ULS+ incorporates these additional datasets and uses smaller input image sizes, resulting in higher accuracy and faster inference. We compared ULS and ULS+ using the Dice score and robustness to click-point location on the ULS23 Challenge test data and a subset of the Longitudinal-CT dataset. In all comparisons, ULS+ significantly outperformed ULS. Additionally, ULS+ ranks first on the ULS23 Challenge test-phase leaderboard. By maintaining a cycle of data-driven updates and clinical validation, ULS+ establishes a foundation for robust and clinically relevant lesion segmentation models.
