Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:17 AM
Ignite Modification Date:
2025-12-25 @ 1:17 AM
NCT ID:
NCT00995293
Eligibility Criteria:
Inclusion criteria:
* Tumor type: Histologically or cytologically proven squamous cell carcinoma of the head and neck (SCCHN) presenting with locally advanced disease at diagnosis. Primary tumor sites eligible are: oral cavity, oropharynx, hypopharynx and larynx.
* Extent of the disease:
* Patients are required to have at least one measurable lesion.
* Stage III or IV without evidence of distant metastases, according to the TNM staging system. Absence of metastases must be checked by chest X-ray (with or without Computed tomography (CT) ), abdominal ultrasound or CT in case of liver function test abnormalities, and bone scan in case of local symptoms.
* Tumor considered as inoperable after evaluation by a multidisciplinary team. Reason for inoperability will be reported in the CRF
* World Health Organization (WHO) performance status 0 or 1
* Laboratory data:
* Haematology:
* Neutrophil count \> or = 2.0\*10\^9/L
* Platelet count \> or = 100\*10\^9/L
* Hemoglobin \> or = 10 g/dl (6.2 mmol/L)
* Hepatic function:
* Total serum bilirubin \< or = 1 time the upper normal limit (UNL) of the participating center
* Aspartate transaminase (ASAT/SGOT) and Alanine transaminase (ALAT/SGPT) \< or = 2.5UNL
* Alkaline phosphatase \< or = 5 UNL
* Patients with ASAT or ALAT \> 1.5UNL associated with alkaline phosphatase \>2.5UNL are not eligible for the study
* Renal function:
* serum creatinine \< or = 120µmol/L (1.4 mg/dl) if values are \>120µmol/L, creatinine clearance should be \> or = 60 ml/min
* Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule, those conditions should be discussed with the patient before registration in the trial
* Patients informed consent form obtained
Exclusion criteria:
* Tumors of the nasopharynx, the nasal and paranasal cavities.
* Previous chemotherapy or radiotherapy for any reason and previous surgery for SCCHN at time of study entry.
* Prior treatment within a therapeutic clinical tria within 30 days prior to study entry
* Concurrent treatment with any other anticancer therapy
* Chronic treatment (\> or = 3 months) with corticosteroids at a daily dose \> or = 20mg methylprednisolone or equivalent.
* Concomitant use of drugs which could interact with 5-fluorouracil (e.g. cimetidine, allopurinol, folic or folinic acid, methotrexate and metronidazole)
* Previous or current malignancies at other sites with the exception of adequately treated in situ carcinoma of the cervix uteri, basal or squamous cell carcinoma of the skin or other cancer curatively treated by surgery and with no evidence of disease for at least 5 years
* Symptomatic peripheral neuropathy \> or = grade 2 by NCIC-CTG criteria
* Clinical altered hearing
* Pregnant, lactating women or of childbearing potential unless adequate
* with other serious illness or medical condition including but not limited to:
* unstable cardiac disease despite treatment
* myocardial infarction within 6 months prior to study entry
* history of significant neurologic or psychiatric disorders including dementia or seizures
* active uncontrolled infection
* active peptic ulcer
* chronic obstructive pulmonary disease requiring hospitalization during the year preceding study entry
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT00995293
Study Brief:
Protocol Section:
NCT00995293