With the protocol defined in the initialisation phase of the trial, the datasets can be prepared. Following the inclusion criteria, DICOM CT, FDG-PET and/or MR images of patients are gathered. Delineations of targets and organs-at-risk are created in DICOM RT Struct format.
After de-identifying the datasets, they are uploaded to the secured database that is set up for the project.
Refer to the Quality Assurance (QA) page for more information on the QA procedures that are applied to the datasets.
Click on the blocks in the image to get more information about their contents.