The US National Institutes of Health state that Sharing of clinical trial data has great potential to accelerate scientific progress and ultimately improve public health by generating better evidence on the safety and effectiveness of therapies for patients (https://www.ncbi.nlm.nih.gov/books/NBK285999/ accessed 2024-01-24.). Aligned with this initiative, the Trial Management Committee of the Trans-Tasman Radiation Oncology Group (TROG) 15.01 Stereotactic Prostate Adaptive Radiotherapy utilizing Kilovoltage intrafraction monitoring (KIM) (SPARK) clinical trial supported the public sharing of the clinical trial data. The data originate from the TROG 15.01 SPARK clinical trial. The SPARK trial was a phase II prospective multi-institutional clinical trial (NCT02397317). The aim of the SPARK clinical trial was to measure the geometric and dosimetric cancer targeting accuracy achieved with a real-time image-guided radiotherapy technology named KIM for 48 prostate cancer patients treated in 5 treatment sessions. During treatment, real-time tumor translational and rotational motion were determined from x-ray images using the KIM technology. A dose reconstruction method was used to evaluate the dose delivered to the target and organs-at-risk. Patient-reported outcomes and toxicity data were monitored up to 2 years after the completion of the treatment. The dataset contains planning CT images, treatment plans, structure sets, planned and motion-included dose-volume histograms, intrafraction kilovoltage, and megavoltage projection images, tumor translational and rotational motion determined by KIM, tumor motion ground truth data, the linear accelerator trajectory traces, and patient treatment outcomes. The dataset is publicly hosted by the University of Sydney eScholarship Repository at https://doi.org/10.25910/qg5d-6058. The 3.6Tb dataset, with approximately 1 million patient images, could be used for a variety of applications, including the development of real-time image-guided methods, adaptation strategies, tumor, and normal tissue control modeling, and prostate-specific antigen kinetics.
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