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. 2025 Jul 4;10(9):101845.
doi: 10.1016/j.adro.2025.101845. eCollection 2025 Sep.

Deep Learning-Based Cardiac Chamber Segmentation in Magnetic Resonance-Guided Adaptive Radiation Therapy

Affiliations

Deep Learning-Based Cardiac Chamber Segmentation in Magnetic Resonance-Guided Adaptive Radiation Therapy

Xinru Chen et al. Adv Radiat Oncol. .

Abstract

Purpose: Accurate cardiac chamber segmentation is crucial for improving cardiac sparing in magnetic resonance (MR)-guided adaptive radiation therapy, especially in patients at risk for radiation-induced cardiotoxicity. Here, we developed and evaluated automatic segmentation models for cardiac chambers that use daily MR images acquired on a 1.5-T MR-Linac system.

Methods and materials: Twenty healthy volunteers underwent daily MR scanning on a 1.5-T MR-Linac, with 2 radial sequences: T2/T1 3DVaneXD balanced fast field echo with spectral attenuated inversion recovery (bFFE-SPAIR) and T1 3DVaneXD mDixon. Three flip angles were tested for each sequence to determine optimal image quality for chamber segmentation. Full-resolution 3D nnU-Net models were trained for the following: (1) bFFE-SPAIR (bFFE model); (2) T1 mDixon (mDixon model); and (3) both sequences (hybrid model). Models were evaluated based on Dice similarity coefficient (DSC) and mean surface distance against manual contours. Clinical acceptance of the automatic segmentation was assessed with a 5-point Likert scale. An in-silico planning study was performed to assess cardiac chamber sparing during plan adaptation.

Results: The average contrast-to-noise ratios in bFFE-SPAIR were 8.7 (20°), 34.2 (50°), and 37.3 (80°); for T1 mDixon, these values were 3.6 (5°), 5.9 (10°), and 4.9 (20°). The bFFE model achieved the highest segmentation performance (average DSC 0.85 ± 0.05 and mean surface distance 2.2 ± 0.6 mm). The T1 mDixon sequence, despite lower contrast-to-noise ratios, provided similar segmentation accuracy (DSC 0.83 ± 0.06). A hybrid model combining both sequences showed no significant improvement over the bFFE model. Clinical evaluation indicated that 95% of the autosegmented contours from the bFFE model were acceptable for clinical use (score ≥4). Adaptive plan greatly reduced individual cardiac chamber dose while maintaining similar target coverage.

Conclusions: This study demonstrated the feasibility of using bFFE-SPAIR and T1 mDixon sequences to accurately segment cardiac chambers on a 1.5-T MR-Linac. These models offer potential for improved cardiac sparing in MR-guided adaptive radiation therapy.

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Conflict of interest statement

Zhongxing Liao reports financial support was provided by National Institutes of Health. Jinzhong Yang reports financial support, article publishing charges, and travel were provided by Radiation Oncology Institute. The other authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Figure 1
Figure 1
Comparison of (A1-A3): bFFE 3DVaneXD SPAIR images and (B1-B3): T1 3DVaneXD mDixon (water) images acquired at different flip angles (FAs). Each row is demonstrated with the same window and level. Abbreviation: bFFE-SPAIR = balanced fast field echo with spectral attenuated inversion recovery.
Figure 2
Figure 2
Demonstration of a good and a poor case of cardiac chamber autosegmentation. (A1, B1), manual contours; (A2, B2), auto contours from bFFE model; (A3, B3), auto contours from mDixon model; and (A4, B4), auto contours from hybrid model. Notably, the auto contours in A3 and B3 are superimposed on T1 mDixon images (water contrast), and the others are shown on bFFE-SPAIR images. Abbreviation: bFFE-SPAIR = balanced fast field echo with spectral attenuated inversion recovery.
Figure 3
Figure 3
Demonstration of in-silico plan adaptation for cardiac chamber dose sparing. (A) Dosimetric criteria with dose statistics from the adaptive plan (70SBRTADT03) and the reference plan (70SBRT). (B) Dose distributions for the reference plan (B1) and adaptive plan (B2). (C) Dose-volume histograms (DVHs) for planning target volume (PTV), internal clinical target volume (iCTV), and other organs, with color coding listed in (A).

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