Phase
Condition
N/ATreatment
De-escalation of irradiated volume
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients with a newly diagnosed (no pre-treatment) squamous cell carcinoma of theoropharynx (i.e. tonsils, base of tongue, oropharyngeal walls, oropharyngeal surfaceof epiglottis; ICD-10 codes C01, C09, C10), T1-4, N0-3.
Treatment with definitive (chemo) radiotherapy planned, with elective irradiation ofthe 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 andneck surgeon and/or radiation oncologist.
FDG-PET scan prior to study inclusion. In case of inability to perform orcontra-indication, at least contrast enhanced MRI scan obligatory.
Participants need to provide informed consent.
Exclusion
Exclusion Criteria:
Inclusion Criteria:
Patients with a newly diagnosed (no pre-treatment) squamous cell carcinoma of theoropharynx (i.e. tonsils, base of tongue, oropharyngeal walls, oropharyngeal surfaceof epiglottis; ICD-10 codes C01, C09, C10), T1-4, N0-3.
Treatment with definitive (chemo) radiotherapy planned, with elective irradiation ofthe 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 andneck surgeon and/or radiation oncologist.
FDG-PET scan prior to study inclusion. In case of inability to perform orcontra-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 theoral cavity, naso- or hypopharynx
Distant metastases detected.
Previous surgery, chemotherapy or radiotherapy treatment for other head and neckcancers.
Previous surgery in head and neck region affecting the cervical lymphatic system.Dissection of singular lymph nodes for diagnostic purposes before treatment start isallowed.
Synchronous or previous malignancies. Exceptions are curatively treated basal cellcarcinoma or SCC of the skin, or in situ carcinoma of the cervix uteri, low- orintermediate- risk prostate cancer or breast with a progression-free follow-up timeof at least 3 years without any remaining disease burden, or other previousmalignancy with a progression-free interval of at least 5 years without anyremaining active/progressive disease burden regardless whether the treatment iscompleted or ongoing as a maintenance treatment (e.g. androgen deprivation therapyfor prostate cancer).
Pregnancy or breast feeding
Any severe mental or psychic disorder affecting decision making and ability toprovide informed consent.
Study Design
Study Description
Connect with a study center
Zurich University Hospital
Zurich 2657896, Canton of Zurich 2657895 8091
SwitzerlandActive - Recruiting
Cantonal Hospital Aarau
Aarau,
SwitzerlandSite Not Available
Cantonal Hospital Aarau
Aarau 2661881,
SwitzerlandActive - Recruiting
Ospedale Regionale di Bellinzona
Bellinzona,
SwitzerlandSite Not Available
Ospedale Regionale di Bellinzona
Bellinzona 2661567,
SwitzerlandActive - Recruiting
Inselspital Bern
Bern,
SwitzerlandSite Not Available
Inselspital Bern
Bern 2661552,
SwitzerlandActive - Recruiting
Hôpitaux universitaires de Genève
Geneva 2660646,
SwitzerlandActive - Recruiting
Zurich University Hospital
Zurich, 8091
SwitzerlandSite Not Available

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