Personalized Volume-deescalated Elective Nodal Irradiation in Oropharyngeal Head and Neck Squamous Cell Carcinoma

Recruiting Phase 2 Interventional Study
Oropharynx Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
University of Zurich · Other
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About This Trial

Multicentric prospective model-based de-escalation of the elective clinical target volumes (CTV) in radiotherapy of oropharyngeal carcinoma of all stages with the goal to reduce toxicity. The study investigates the feasibility of this approach as measured by the number of expected out-of-field recurrencies based on the individual patient's state of disease progression and risk factors

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients with a newly diagnosed (no pre-treatment) squamous cell carcinoma of the oropharynx (i.e. tonsils, base of tongue, oropharyngeal walls, oropharyngeal surface of epiglottis; ICD-10 codes C01, C09, C10), T1-4, N0-3. * Treatment with definitive (chemo) radiotherapy plann…
Contacts

Panagiotis Balermpas, MD

+41 44 255 35 67

Panagiotis.Balermpas@usz.ch

CONTACT

Debra Lauer, MSc

+41 43 253 28 17

RAO_Akademischesoffice@usz.ch

CONTACT