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Register a new userFully automated 3D segmentation of dopamine transporter SPECT images using an estimation-based approach
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Quantitative measures of uptake in caudate, putamen, and globus pallidus in dopamine transporter (DaT) brain SPECT have potential as biomarkers for the severity of Parkinson disease. Reliable quantification of uptake requires accurate segmentation of these regions. However, segmentation is challenging in DaT SPECT due to partial-volume effects, system noise, physiological variability, and the small size of these regions. To address these challenges, we propose an estimation-based approach to segmentation. This approach estimates the posterior mean of the fractional volume occupied by caudate, putamen, and globus pallidus within each voxel of a 3D SPECT image. The estimate is obtained by minimizing a cost function based on the binary cross-entropy loss between the true and estimated fractional volumes over a population of SPECT images, where the distribution of the true fractional volumes is obtained from magnetic resonance images from clinical populations. The proposed method accounts for both the sources of partial-volume effects in SPECT, namely the limited system resolution and tissue-fraction effects. The method was implemented using an encoder-decoder network and evaluated using realistic clinically guided SPECT simulation studies, where the ground-truth fractional volumes were known. The method significantly outperformed all other considered segmentation methods and yielded accurate segmentation with dice similarity coefficients of ~ 0.80 for all regions. The method was relatively insensitive to changes in voxel size. Further, the method was relatively robust up to +/- 10 degrees of patient head tilt along transaxial, sagittal, and coronal planes. Overall, the results demonstrate the efficacy of the proposed method to yield accurate fully automated segmentation of caudate, putamen, and globus pallidus in 3D DaT-SPECT images.
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Image reconstruction in Single Photon Emission Computed Tomography (SPECT) is affected by physical effects such as photon attenuation, Compton scatter and detector response. These effects can be compensated for by modeling the corresponding spread of photons in 3D within the system matrix used for tomographic reconstruction. The fully 3D Monte Carlo (F3DMC) reconstruction technique consists in calculating this system matrix using Monte Carlo simulations. The inverse problem of tomographic reconstruction is then solved using conventional iterative algorithms such as maximum likelihood expectation maximization (MLEM). Although F3DMC has already shown promising results, its use is currently limited by two major issues: huge size of the fully 3D system matrix and long computation time required for calculating a robust and accurate system matrix. To address these two issues, we propose to calculate the F3DMC system matrix using a spatial sampling matching the functional regions to be reconstructed. In this approach, different regions of interest can be reconstructed with different spatial sampling. For instance, a single value is reconstructed for a functional region assumed to contain uniform activity. To assess the value of this approach, Monte Carlo simulations have been performed using GATE. Results suggest that F3DMC reconstruction using functional regions improves quantitative accuracy compared to the F3DMC reconstruction method proposed so far. In addition, it considerably reduces disk space requirement and duration of the simulations needed to estimate the system matrix. The concept of functional regions might therefore make F3DMC reconstruction practically feasible.
Tumor segmentation in oncological PET is challenging, a major reason being the partial-volume effects due to the low system resolution and finite voxel size. The latter results in tissue-fraction effects, i.e. voxels contain a mixture of tissue classes. Most conventional methods perform segmentation by exclusively assigning each voxel in the image as belonging to either the tumor or normal tissue classes. Thus, these methods are inherently limited in modeling the tissue-fraction effects. To address this inherent limitation, we propose an estimation-based approach to segmentation. Specifically, we develop a Bayesian method that estimates the posterior mean of fractional volume that the tumor occupies within each image voxel. The proposed method, implemented using an encoder-decoder network, was first evaluated using clinically realistic 2-D simulation studies with known ground truth, in the context of segmenting the primary tumor in PET images of patients with lung cancer. The evaluation studies demonstrated that the method accurately estimated the tumor-fraction areas and significantly outperformed widely used conventional methods, including a U-net-based method, on the task of segmenting the tumor. In addition, the proposed method was relatively insensitive to partial-volume effects and yielded reliable tumor segmentation for different clinical-scanner configurations. The method was then evaluated using clinical images of patients with stage II and III non-small cell lung cancer from ACRIN 6668/RTOG 0235 multi-center clinical trial. Here, the results showed that the proposed method significantly outperformed all other considered methods and yielded accurate tumor segmentation on patient images with dice similarity coefficient of 0.82 (95% CI: 0.78, 0.86). Overall, this study demonstrates the efficacy of the proposed method to accurately segment tumors in PET images.
In SPECT, list-mode (LM) format allows storing data at higher precision compared to binned data. There is significant interest in investigating whether this higher precision translates to improved performance on clinical tasks. Towards this goal, in this study, we quantitatively investigated whether processing data in LM format, and in particular, the energy attribute of the detected photon, provides improved performance on the task of absolute quantification of region-of-interest (ROI) uptake in comparison to processing the data in binned format. We conducted this evaluation study using a DaTscan brain SPECT acquisition protocol, conducted in the context of imaging patients with Parkinsons disease. This study was conducted with a synthetic phantom. A signal-known exactly/background-known-statistically (SKE/BKS) setup was considered. An ordered-subset expectation-maximization algorithm was used to reconstruct images from data acquired in LM format, including the scatter-window data, and including the energy attribute of each LM event. Using a realistic 2-D SPECT system simulation, quantification tasks were performed on the reconstructed images. The results demonstrated improved quantification performance when LM data was used compared to binning the attributes in all the conducted evaluation studies. Overall, we observed that LM data, including the energy attribute, yielded improved performance on absolute quantification tasks compared to binned data.
The MR-Linac is a combination of an MR-scanner and radiotherapy linear accelerator (Linac) which holds the promise to increase the precision of radiotherapy treatments with MR-guided radiotherapy by monitoring motion during radiotherapy with MRI, and adjusting the radiotherapy plan accordingly. Optimal MR-guidance for respiratory motion during radiotherapy requires MR-based 3D motion estimation with a latency of 200-500 ms. Currently this is still challenging since typical methods rely on MR-images, and are therefore limited by the 3D MR-imaging latency. In this work, we present a method to perform non-rigid 3D respiratory motion estimation with 170 ms latency, including both acquisition and reconstruction. The proposed method called real-time low-rank MR-MOTUS reconstructs motion-fields directly from k-space data, and leverages an explicit low-rank decomposition of motion-fields to split the large scale 3D+t motion-field reconstruction problem posed in our previous work into two parts: (I) a medium-scale offline preparation phase and (II) a small-scale online inference phase which exploits the results of the offline phase for real-time computations. The method was validated on free-breathing data of five volunteers, acquired with a 1.5T Elekta Unity MR-Linac. Results show that the reconstructed 3D motion-field are anatomically plausible, highly correlated with a self-navigation motion surrogate (R = 0.975 +/- 0.0110), and can be reconstructed with a total latency of 170 ms that is sufficient for real-time MR-guided abdominal radiotherapy.
Objectives: Precise segmentation of total extraocular muscles (EOM) and optic nerve (ON) is essential to assess anatomical development and progression of thyroid-associated ophthalmopathy (TAO). We aim to develop a semantic segmentation method based on deep learning to extract the total EOM and ON from orbital CT images in patients with suspected TAO. Materials and Methods: A total of 7,879 images obtained from 97 subjects who underwent orbit CT scans due to suspected TAO were enrolled in this study. Eighty-eight patients were randomly selected into the training/validation dataset, and the rest were put into the test dataset. Contours of the total EOM and ON in all the patients were manually delineated by experienced radiologists as the ground truth. A three-dimensional (3D) end-to-end fully convolutional neural network called semantic V-net (SV-net) was developed for our segmentation task. Intersection over Union (IoU) was measured to evaluate the accuracy of the segmentation results, and Pearson correlation analysis was used to evaluate the volumes measured from our segmentation results against those from the ground truth. Results: Our model in the test dataset achieved an overall IoU of 0.8207; the IoU was 0.7599 for the superior rectus muscle, 0.8183 for the lateral rectus muscle, 0.8481 for the medial rectus muscle, 0.8436 for the inferior rectus muscle and 0.8337 for the optic nerve. The volumes measured from our segmentation results agreed well with those from the ground truth (all R>0.98, P<0.0001). Conclusion: The qualitative and quantitative evaluations demonstrate excellent performance of our method in automatically extracting the total EOM and ON and measuring their volumes in orbital CT images. There is a great promise for clinical application to assess these anatomical structures for the diagnosis and prognosis of TAO.
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