EichorEICHOR
Study identifier: NCT06563362 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingDeEscO

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

Condition: Oropharynx Cancer  ·  Sponsor: University of Zurich

PhasePhase 2
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where6 locations

Interested? Contact the study team ↓

For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

Panagiotis Balermpas, MD  ·  +41 44 255 35 67  ·  Panagiotis.Balermpas@usz.ch

Debra Lauer, MSc  ·  +41 43 253 28 17  ·  RAO_Akademischesoffice@usz.ch

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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 planned, with elective irradiation of the lymph nodes. * Age ≥ 18 years, no upper age limit. * ECOG performance score \< 3. * History/physical examination within 30 days prior to study inclusion by head and neck surgeon and/or radiation oncologist. * FDG-PET scan prior to study inclusion. In case of inability to perform or contra-indication, at least contrast enhanced MRI scan obligatory. * Participants need to provide informed consent. Exclusion 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 planned, with elective irradiation of the lymph nodes. * Age ≥ 18 years, no upper age limit. * ECOG performance score \< 3. * History/physical examination within 30 days prior to study inclusion by head and neck surgeon and/or radiation oncologist. * FDG-PET scan prior to study inclusion. In case of inability to perform or contra-indication, at least contrast enhanced MRI scan obligatory. * Participants need to provide informed consent. Exclusion Criteria: * Multilevel primary tumors extending unambiguously beyond the oropharynx into the oral cavity, naso- or hypopharynx * Distant metastases detected. * Previous surgery, chemotherapy or radiotherapy treatment for other head and neck cancers. * Previous surgery in head and neck region affecting the cervical lymphatic system. Dissection of singular lymph nodes for diagnostic purposes before treatment start is allowed. * Synchronous or previous malignancies. Exceptions are curatively treated basal cell carcinoma or SCC of the skin, or in situ carcinoma of the cervix uteri, low- or intermediate- risk prostate cancer or breast with a progression-free follow-up time of at least 3 years without any remaining disease burden, or other previous malignancy with a progression-free interval of at least 5 years without any remaining active/progressive disease burden regardless whether the treatment is completed or ongoing as a maintenance treatment (e.g. androgen deprivation therapy for prostate cancer). * Pregnancy or breast feeding * Any severe mental or psychic disorder affecting decision making and ability to provide informed consent.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (6)

Zurich University HospitalZurich, Canton of Zurich, SwitzerlandRecruiting
Cantonal Hospital AarauAarau, SwitzerlandRecruiting
Ospedale Regionale di BellinzonaBellinzona, SwitzerlandRecruiting
Inselspital BernBern, SwitzerlandRecruiting
Hôpitaux universitaires de GenèveGeneva, SwitzerlandRecruiting
Réseau Hospitalier NeuchâteloisNeuchâtel, SwitzerlandRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

ZurichAarauBellinzonaBern

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.

Look up another condition
Look up another city
Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →