About this trial
This prospective in-silico study evaluates a novel Off-line Adaptive Proton Therapy (o-APT) workflow for patients with oropharyngeal cancer receiving proton therapy. The study assesses whether automated image analysis, treatment plan adaptation, and quality assurance can identify and prepare treatment plan modifications more efficiently than current clinical practice, without affecting patient care.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Oropharyngeal cancer patients
Planned for curatively intended proton therapy
Treated with definitive radiotherapy, chemoradiation, or bioradiation
Provided informed consent according to Standard Follow-up Program (SFP) for using data for research
Disqualifiers
None
Trial population
Patients with oropharyngeal cancer receiving curatively intended proton therapy at the University Medical Center Groningen (UMCG)
Trial design
Cohort
Prospective
Treatments tested in this trial
Off-line Adaptive Proton Therapy (o-APT) Workflow Evaluation
Other interventionEvaluation of an off-line adaptive proton therapy workflow using routinely collected clinical data
Treatment groups
Trial outcomes
Primary outcomes
Dose Adjustments Ready to Use Before the Next Fraction
Availability of adapted treatment plans before the next treatment fraction
Secondary outcomes
Accuracy of early identification of the need for treatment plan adaptation
Accuracy of the o-APT workflow in identifying the need for treatment plan adaptation, with particular focus on positive predictive value and negative predictive value.
Sponsors and contacts
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