A convolutional neural network model for EPID-based non-transit dosimetry.

PURPOSE: To develop an alternative computational approach for EPID-based non-transit dosimetry using a convolutional neural network model. METHOD: A U-net followed by a non-trainable layer named True Dose Modulation recovering the spatialized information was developed. The model was trained on 186 Intensity-Modulated Radiation Therapy Step & Shot beams from 36 treatment plans of different tumor locations to convert grayscale portal images into planar absolute dose distributions. Input data were acquired from an amorphous-Silicon Electronic Portal Image Device and a 6 MV X-ray beam. Ground truths were computed from a conventional kernel-based dose algorithm. The model was trained by a two-step learning process and validated through a five-fold cross-validation procedure with sets of training and validation of 80% and 20%, respectively. A study regarding the dependance of the amount of training data was conducted. The performance of the model was evaluated from a quantitative analysis based the ϒ-index, absolute and relative errors computed between the inferred dose distributions and ground truths for six square and 29 clinical beams from seven treatment plans. These results were also compared to those of an existing portal image-to-dose conversion algorithm. RESULTS: For the clinical beams, averages of ϒ-index and ϒ-passing rate (2%-2mm > 10% Dmax ) of 0.24 (±0.04) and 99.29 (±0.70)% were obtained. For the same metrics and criteria, averages of 0.31 (±0.16) and 98.83 (±2.40)% were obtained with the six square beams. Overall, the developed model performed better than the existing analytical method. The study also showed that sufficient model accuracy can be achieved with the amount of training samples used. CONCLUSION: A deep learning-based model was developed to convert portal images into absolute dose distributions. The accuracy obtained shows that this method has great potential for EPID-based non-transit dosimetry.

Parameter estimation of perfusion models in dynamic contrast-enhanced imaging: a unified framework for model comparison.

Patients follow-up in oncology is generally performed through the acquisition of dynamic sequences of contrast-enhanced images. Estimating parameters of appropriate models of contrast intake diffusion through tissues should help characterizing the tumour physiology. However, several models have been developed and no consensus exists on their clinical use. In this paper, we propose a unified framework to analyse models of perfusion and estimate their parameters in order to obtain reliable and relevant parametric images. After defining the biological context and the general form of perfusion models, we propose a methodological framework for model assessment in the context of parameter estimation from dynamic imaging data: global sensitivity analysis, structural and practical identifiability analysis, parameter estimation and model comparison. Then, we apply our methodology to five of the most widely used compartment models (Tofts model, extended Tofts model, two-compartment model, tissue-homogeneity model and distributed-parameters model) and illustrate the results by analysing the behaviour of these models when applied to data acquired on five patients with abdominal tumours.

Registration of free-breathing 3D+t abdominal perfusion CT images via co-segmentation.

Dynamic contrast-enhanced computed tomography (DCE-CT) is a valuable imaging modality to assess tissues properties, particularly in tumours, by estimating pharmacokinetic parameters from the evolution of pixels intensities in 3D+t acquisitions. However, this requires a registration of the whole sequence of volumes, which is challenging especially when the patient breathes freely. In this paper, we propose a generic, fast and automatic method to address this problem. As standard iconic registration methods are not robust to contrast intake, we rather rely on the segmentation of the organ of interest. This segmentation is performed jointly with the registration of the sequence within a novel co-segmentation framework. Our approach is based on implicit template deformation, that we extend to a co-segmentation algorithm which provides as outputs both a segmentation of the organ of interest in every image and stabilising transformations for the whole sequence. The proposed method is validated on 15 datasets acquired from patients with renal lesions and shows improvement in terms of registration and estimation of pharmacokinetic parameters over the state-of-the-art method.

A multi-task learning approach for compartmental model parameter estimation in DCE-CT sequences.

Today's follow-up of patients presenting abdominal tumors is generally performed through acquisition of dynamic sequences of contrast-enhanced CT. Estimating parameters of appropriate models of contrast intake diffusion through tissues should help characterizing the tumor physiology, but is impeded by the high level of noise inherent to the acquisition conditions. To improve the quality of estimation, we consider parameter estimation in voxels as a multi-task learning problem (one task per voxel) that takes advantage from the similarity between two tasks. We introduce a temporal similarity between tasks based on a robust distance between observed contrast-intake profiles of intensity. Using synthetic images, we compare multi-task learning using this temporal similarity, a spatial similarity and a single-task learning. The similarities based on temporal profiles are shown to bring significant improvements compared to the spatial one. Results on real CT sequences also confirm the relevance of the approach.