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Deformation Driven Seq2Seq Longitudinal Tumor and Organs-at-Risk Prediction for Radiotherapy

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 Added by Saad Nadeem
 Publication date 2021
and research's language is English




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Purpose: Radiotherapy presents unique challenges and clinical requirements for longitudinal tumor and organ-at-risk (OAR) prediction during treatment. The challenges include tumor inflammation/edema and radiation-induced changes in organ geometry, whereas the clinical requirements demand flexibility in input/output sequence timepoints to update the predictions on rolling basis and the grounding of all predictions in relationship to the pre-treatment imaging information for response and toxicity assessment in adaptive radiotherapy. Methods: To deal with the aforementioned challenges and to comply with the clinical requirements, we present a novel 3D sequence-to-sequence model based on Convolution Long Short Term Memory (ConvLSTM) that makes use of series of deformation vector fields (DVF) between individual timepoints and reference pre-treatment/planning CTs to predict future anatomical deformations and changes in gross tumor volume as well as critical OARs. High-quality DVF training data is created by employing hyper-parameter optimization on the subset of the training data with DICE coefficient and mutual information metric. We validated our model on two radiotherapy datasets: a publicly available head-and-neck dataset (28 patients with manually contoured pre-, mid-, and post-treatment CTs), and an internal non-small cell lung cancer dataset (63 patients with manually contoured planning CT and 6 weekly CBCTs). Results: The use of DVF representation and skip connections overcomes the blurring issue of ConvLSTM prediction with the traditional image representation. The mean and standard deviation of DICE for predictions of lung GTV at week 4, 5, and 6 were 0.83$pm$0.09, 0.82$pm$0.08, and 0.81$pm$0.10, respectively, and for post-treatment ipsilateral and contralateral parotids, were 0.81$pm$0.06 and 0.85$pm$0.02.



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58 - Mikael Agn 2018
In this paper we present a method for simultaneously segmenting brain tumors and an extensive set of organs-at-risk for radiation therapy planning of glioblastomas. The method combines a contrast-adaptive generative model for whole-brain segmentation with a new spatial regularization model of tumor shape using convolutional restricted Boltzmann machines. We demonstrate experimentally that the method is able to adapt to image acquisitions that differ substantially from any available training data, ensuring its applicability across treatment sites; that its tumor segmentation accuracy is comparable to that of the current state of the art; and that it captures most organs-at-risk sufficiently well for radiation therapy planning purposes. The proposed method may be a valuable step towards automating the delineation of brain tumors and organs-at-risk in glioblastoma patients undergoing radiation therapy.
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A 3D deep learning model (OARnet) is developed and used to delineate 28 H&N OARs on CT images. OARnet utilizes a densely connected network to detect the OAR bounding-box, then delineates the OAR within the box. It reuses information from any layer to subsequent layers and uses skip connections to combine information from different dense block levels to progressively improve delineation accuracy. Training uses up to 28 expert manual delineated (MD) OARs from 165 CTs. Dice similarity coefficient (DSC) and the 95th percentile Hausdorff distance (HD95) with respect to MD is assessed for 70 other CTs. Mean, maximum, and root-mean-square dose differences with respect to MD are assessed for 56 of the 70 CTs. OARnet is compared with UaNet, AnatomyNet, and Multi-Atlas Segmentation (MAS). Wilcoxon signed-rank tests using 95% confidence intervals are used to assess significance. Wilcoxon signed ranked tests show that, compared with UaNet, OARnet improves (p<0.05) the DSC (23/28 OARs) and HD95 (17/28). OARnet outperforms both AnatomyNet and MAS for DSC (28/28) and HD95 (27/28). Compared with UaNet, OARnet improves median DSC up to 0.05 and HD95 up to 1.5mm. Compared with AnatomyNet and MAS, OARnet improves median (DSC, HD95) by up to (0.08, 2.7mm) and (0.17, 6.3mm). Dosimetrically, OARnet outperforms UaNet (Dmax 7/28; Dmean 10/28), AnatomyNet (Dmax 21/28; Dmean 24/28), and MAS (Dmax 22/28; Dmean 21/28). The DenseNet architecture is optimized using a hybrid approach that performs OAR-specific bounding box detection followed by feature recognition. Compared with other auto-delineation methods, OARnet is better than or equal to UaNet for all but one geometric (Temporal Lobe L, HD95) and one dosimetric (Eye L, mean dose) endpoint for the 28 H&N OARs, and is better than or equal to both AnatomyNet and MAS for all OARs.
140 - Hyemin Um , Jue Jiang , Maria Thor 2020
We implemented and evaluated a multiple resolution residual network (MRRN) for multiple normal organs-at-risk (OAR) segmentation from computed tomography (CT) images for thoracic radiotherapy treatment (RT) planning. Our approach simultaneously combines feature streams computed at multiple image resolutions and feature levels through residual connections. The feature streams at each level are updated as the images are passed through various feature levels. We trained our approach using 206 thoracic CT scans of lung cancer patients with 35 scans held out for validation to segment the left and right lungs, heart, esophagus, and spinal cord. This approach was tested on 60 CT scans from the open-source AAPM Thoracic Auto-Segmentation Challenge dataset. Performance was measured using the Dice Similarity Coefficient (DSC). Our approach outperformed the best-performing method in the grand challenge for hard-to-segment structures like the esophagus and achieved comparable results for all other structures. Median DSC using our method was 0.97 (interquartile range [IQR]: 0.97-0.98) for the left and right lungs, 0.93 (IQR: 0.93-0.95) for the heart, 0.78 (IQR: 0.76-0.80) for the esophagus, and 0.88 (IQR: 0.86-0.89) for the spinal cord.
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