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
Ospedale Regionale di Bellinzona
Bellinzona,
SwitzerlandActive - Recruiting
Zurich University Hospital
Zurich, 8091
SwitzerlandActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.