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Sara Kurkowska

Publications and source records attributed to Sara Kurkowska.

3 recordsLinked to original sources

Comprehensive framework for evaluation of deep neural networks in detection and quantification of lymphoma from PET/CT images: clinical insights, pitfalls, and observer agreement analyses

This study addresses critical gaps in automated lymphoma segmentation from PET/CT images, focusing on issues often overlooked in existing literature. While deep learning has been applied for lymphoma lesion segmentation, few studies incorporate out-of-distribution testing, raising concerns about model generalizability across diverse imaging conditions and patient populations. We highlight the need to compare model performance with expert human annotators, including intra- and inter-observer variability, to understand task difficulty better. Most approaches focus on overall segmentation accuracy but overlook lesion-specific measures important for precise lesion detection and disease quantification. To address these gaps, we propose a clinically relevant framework for evaluating deep segmentation networks. Using this lesion measure-specific evaluation, we assess the performance of four deep networks (ResUNet, SegResNet, DynUNet, and SwinUNETR) across 611 cases from multi-institutional datasets, covering various lymphoma subtypes and lesion characteristics. Beyond standard metrics like the Dice similarity coefficient, we evaluate clinical lesion measures and their prediction errors. We also introduce detection criteria for lesion localization and propose a new detection Criterion 3 based on metabolic characteristics. We show that networks perform better on large, intense lesions with higher metabolic activity. Finally, we compare network performance to physicians via intra- and inter-observer variability analyses, demonstrating that network errors closely resemble those made by experts, i.e., the small and faint lesions remain challenging for both humans and networks. This study aims to improve automated lesion segmentation's clinical relevance, supporting better treatment decisions for lymphoma patients. The code is available at: https://github.com/microsoft/lymphoma-segmentation-dnn.

cs.CV

Computationally Efficient Collimator-Detector Response Compensation in High Energy SPECT using 1D Convolutions and Rotations

Modeling of the collimator-detector response (CDR) in SPECT reconstruction enables improved resolution and accuracy, and is thus important for quantitative imaging applications such as dosimetry. The implementation of CDR modeling, however, can become a computational bottleneck when there are substantial components of septal penetration and scatter in the acquired data, since a direct convolution-based approach requires large 2D kernels. This work proposes a 1D convolution and rotation-based CDR model that reduces reconstruction times but maintains consistency with models that employ 2D convolutions. To enable open-source development and use of these models in image reconstruction, we release a SPECTPSFToolbox repository for the PyTomography project on GitHub.

physics.med-ph

Uncertainty Propagation from Projections to Region Counts in Tomographic Imaging: Application to Radiopharmaceutical Dosimetry

Radiopharmaceutical therapies (RPTs) present a major opportunity to improve cancer therapy. Although many current RPTs use the same injected activity for all patients, there is interest in using absorbed dose measurements to enable personalized prescriptions. Image-based absorbed dose calculations incur uncertainties from calibration factors, partial volume effects and segmentation methods. While previously published dose estimation protocols incorporate these uncertainties, they do not account for uncertainty originating from the reconstruction process itself with the propagation of Poisson noise from projection data. This effect should be accounted for to adequately estimate the total uncertainty in absorbed dose estimates. This paper proposes a computationally practical algorithm that propagates uncertainty from projection data through clinical reconstruction algorithms to obtain uncertainties on the total measured counts within volumes of interest (VOIs). The algorithm is first validated on ${}^{177}$Lu and ${}^{225}$Ac phantom data by comparing estimated uncertainties from individual SPECT acquisitions to empirical estimates obtained from multiple acquisitions. It is then applied to (i) Monte Carlo and (ii) multi-time point ${}^{177}$Lu-DOTATATE and ${}^{225}$Ac-PSMA-617 patient data for time integrated activity (TIA) uncertainty estimation. The outcomes of this work are two-fold: (i) the proposed uncertainty algorithm is validated, and (ii) a blueprint is established for how the algorithm can be inform dosimetry protocols via TIA uncertainty estimation. The proposed algorithm is made publicly available in the open-source image reconstruction library PyTomography.

physics.med-ph