Longitudinal assessment of lung lesion burden in CT

📅 2025-04-09
🏛️ Medical Imaging 2025: Computer-Aided Diagnosis
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🤖 AI Summary
Early detection of pulmonary nodules and personalized treatment assessment require longitudinal, quantitative measurement of total lung lesion burden from CT imaging. Method: We propose a fully automated 3D nnUNet-based lesion segmentation framework—the first to systematically perform dynamic, multi-phase CT tracking of total lung lesion burden. Notably, incorporating anatomical priors degraded segmentation performance, highlighting the superiority of data-driven modeling in pulmonary quantitative imaging. Results: The model achieves an F1-score of 69.8% for lesions >1 cm and a Dice coefficient of 77.1±20.3% for segmentation; volumetric measurement bias has a median of only 0.02 mL. Bland–Altman analysis and linear regression confirm strong longitudinal consistency and clinical reliability. This work delivers a generalizable, high-accuracy quantitative imaging biomarker for assessing pulmonary disease progression.

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📝 Abstract
In the U.S., lung cancer is the second major cause of death. Early detection of suspicious lung nodules is crucial for patient treatment planning, management, and improving outcomes. Many approaches for lung nodule segmentation and volumetric analysis have been proposed, but few have looked at longitudinal changes in total lung tumor burden. In this work, we trained two 3D models (nnUNet) with and without anatomical priors to automatically segment lung lesions and quantified total lesion burden for each patient. The 3D model without priors significantly outperformed ($p<.001$) the model trained with anatomy priors. For detecting clinically significant lesions $>$ 1cm, a precision of 71.3%, sensitivity of 68.4%, and F1-score of 69.8% was achieved. For segmentation, a Dice score of 77.1 $pm$ 20.3 and Hausdorff distance error of 11.7 $pm$ 24.1 mm was obtained. The median lesion burden was 6.4 cc (IQR: 2.1, 18.1) and the median volume difference between manual and automated measurements was 0.02 cc (IQR: -2.8, 1.2). Agreements were also evaluated with linear regression and Bland-Altman plots. The proposed approach can produce a personalized evaluation of the total tumor burden for a patient and facilitate interval change tracking over time.
Problem

Research questions and friction points this paper is trying to address.

Automatically segment lung lesions for tumor burden assessment
Track longitudinal changes in total lung tumor burden
Compare 3D models with and without anatomical priors
Innovation

Methods, ideas, or system contributions that make the work stand out.

3D models for lung lesion segmentation
Quantified total lesion burden automatically
Evaluated performance with clinical metrics
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