ESTRO 2022 - Abstract Book

S46

Abstract book

ESTRO 2022

Conclusion We have developed a pipeline to predict segmentations for post-treatment data based on pre-treatment scans, including a method to evaluate the prediction accuracy. The method provided good results, especially for larger brain structures, while the prediction accuracy behavior of all structures was learned correctly.

PD-0071 A novel method for evaluating CBCT-based synthetic CTs

C. Sargeant 1 , A. Green 1 , R. Chuter 1,2 , A. McWilliam 1

1 The University of Manchester, Division of Cancer Sciences – Faculty of Biology, Medicine and Health, Manchester, United Kingdom; 2 The Christie NHS Foundation Trust, Christie Medical Physics and Engineering, Manchester, United Kingdom Purpose or Objective Artificial intelligence (AI) models are increasingly used to generate synthetic CTs (sCTs) from on-treatment CBCTs and hold potential for adaptive radiotherapy. However, lack of a ground truth image hinders the evaluation of sCTs. Commonly, the planning CT (pCT) is deformable registered to the CBCT anatomy to create a deformed CT (dCT) for comparison, but this suffers from inherent uncertainties due to the registration. We propose a novel method to evaluate sCTs using the differences between scans to isolate model and registration accuracy and determine whether sCT is superior to dCT. Materials and Methods For 10 prostate patients, the pCT and all on-treatment CBCTs (range: 6-12 per patient, total 92 images) were collected. ADMIRE v3.29.1 (Elekta AB) was used to generate the dCTs and sCTs for each CBCT; a cycle Generative Adversarial Network (cycleGAN) was used for sCT generation, while a b-spline based registration engine was used to produce dCT. For each time point, the pCT, CBCT, dCT and sCT were rigidly registered and the differences determined. These differences are shown in Fig 1 and are assumed to be derived from the inherent differences between the scans: anatomical differences, image quality, model error and registration error. Each image was masked according to the smallest field of view across modalities. The mean pixel value for each difference was calculated for each time point per patient and compared using a paired intra- patient Mann-Whitney U test. We test for the alternative hypothesis to determine if mean difference in the dCT arm of the comparison is significantly greater than the sCT arm (greater value corresponds to worse performance).

Results In 80% of cases, the sCT outperforms the dCT as indicated by a significantly smaller average pixel value in the model arm of comparisons than the registration arm (Fig 2A). Compared to all other patients, Patients 2 and 6 suffer from severe artefacts across each of the CBCTs. The cycleGAN does not adequately suppress these artefacts, impacting the sCT while the dCT remains unaffected (Fig 2B). While the cycleGAN model was trained with a large number of CT-CBCT prostate pairs, the model appears not to generalise to artefacts in the CBCT, implying a scarcity of artefacts in the training data.

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