IMRT Plus Cisplatin Versus Conventional Radiotherapy Plus Cisplatin in Stage III-IV HNSCC
Oral Cancer, Oropharynx Cancer, Hypopharynx Cancer
About this trial
This is an interventional treatment trial for Oral Cancer focused on measuring oral cancer, oropharynx cancer, hypopharynx cancer, IMRT
Eligibility Criteria
Inclusion Criteria: squamous cell carcinoma of oral cavity, oropharynx or hypopharynx Stage III - IV (T1-T4, N0-N2)(UICC 2002) Not resected Indication of radiotherapy to bilateral cervical nodes at dose>= 50 Gy Delineation of target volumes done before randomization Scintigraphy of parotid gland done before radiotherapy start Quality of life questionnaires (EORTC-C30 and EORTC-H&N35) filled in by the patient Informed consent signed Exclusion Criteria: N3 (UICC 2002) Distant metastasis Contra-indication to concomitant cisplatin History of cancer within the last 5 years History of head and neck radiotherapy Administration of drugs for treatment or prophylaxis of xerostomia (pilocarpine, ethyol)
Sites / Locations
- Centre Alexis Vautrin
- Institut Gustave Roussy
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
1
2
Conventional RT 70Gy + concomitant cisplatin
IMRT 75Gy + concomitant cisplatin