Phase I study to assess the feasibility (i.e. early toxicity) of Molecular Imaging-based Dose Escalation in HPV Negative Patients With Locally Advanced SCC of the Oropharynx.
The objective is to assess the feasibility (i.e. early toxicity) of an adaptive dose escalation through 18F-FDG-PET-based dose painting by numbers in 10 HPV negative patients with locally advanced squamous cell carcinoma of the oropharynx. Treatment will be delivered with Helical Tomotherapy® or volumetric-modulated arc therapy (VMAT). Dose adaptation will be performed at 2 time-points with per-treatment 18F-FDG-PET/CT scans.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
molecular imaging based radiotherapy dose escalation
Cliniques Universitaires Saint Luc
Brussels, Belgium
RECRUITINGU.Z. Leuven - Campus Gasthuisberg
Leuven, Belgium
NOT_YET_RECRUITINGAcute toxicity
Time frame: up to 3 months following the completion of radiotherapy
Primary tumor control probability
Time frame: at 1 and 2 years
Late toxicity
Time frame: at 1 and 2 years
Progression-free survival
Time frame: at 1 and 2 years
Overall survival
Time frame: at 1 and 2 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.