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 @ 12:10 AM
Ignite Modification Date:
2025-12-25 @ 12:10 AM
NCT ID:
NCT01711658
Eligibility Criteria:
Inclusion criteria:
* Patients must have histologically or cytologically confirmed diagnosis (from primary lesion and/or lymph nodes) of Squamous Cell Cancer of the oropharynx, hypopharynx or larynx (For patients with oropharynx primary, the tumor must be negative for p16 by immunohistochemistry).
* Patients with selected Stage III or IV disease (T2 N2-3 M0, T3-4 any N M0, T1 N2b, N2c or N3 p16 negative oropharynx cancer or T1-2 any N+ hypopharynx cancer) including no distant metastases.
* History/Physical examination by a Radiation Oncologist and Medical oncologist prior to entering the study.
* Examination by an ears, nose, throat (ENT) or Head \& Neck Surgeon including laryngopharyngoscopy prior to entering the study.
* Patients must have a chest CT scan, or positron emission tomography (PET)/CT scan to rule out metastatic disease
* Patients must have a contrast enhanced CT scan or MRI or PET/CT scan of the tumor site and neck nodes prior to entering the study.
* Patients must have an EKG and echocardiogram (ECHO) or multigated acquisition (MUGA) scan prior to entering the study.
* Patients must have Zubrod Performance Status of 0-1.
* Patients must be ≥ 18 years of age.
* Patients must have normal organ and marrow function as defined below:
* Absolute neutrophil count (ANC) ≥ 1,500 cells/mm3
* Platelets ≥ 100,000 cells/mm3
* Hemoglobin ≥ 8.0 g/dl
* Serum creatinine \< 1.5 mg/dl or creatinine clearance (CC) ≥ 50 ml/min
* Total bilirubin \< 2 x the institutional upper limit of normal
* Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) ≤ 3 x the institutional upper limit of normal
* Patient must have magnesium, calcium, glucose, potassium and sodium levels within normal limits
* Women of childbearing potential must have a negative pregnancy test prior to registration.
* Patients of reproductive potential must practice effective contraception while on study and for at least 60 calendar days following treatment.
* All patients must sign an informed consent prior to enrollment.
* Patients must comply with the treatment plan and follow-up schedule.
Exclusion criteria:
* Patients with simultaneous primaries or bilateral tumors.
* Patients who have had gross total excision of the primary tumor.
* Patients with initial surgical treatment, radical or modified neck dissection.
* Patients who received prior systemic chemotherapy for the study cancer.
* Patients who received prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields.
* Patients with primary tumor of oral cavity, nasopharynx, sinuses or salivary glands.
* Prior allergic reaction to the study drugs.
* Patients who have had prior therapy that specifically and directly targets the epidermal growth factor receptor (EGFR)/human epidermal growth factor receptor 2 (HER2) pathway.
* Patients who have current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, or stable chronic liver disease per investigator assessment);
* Pregnant women or sexually active patients not willing or able to use medically acceptable forms of contraceptive method while on treatment.
* Patients with severe, active co-morbidity, defined as follows:
* Uncontrolled cardiac disease, such as uncontrolled hypertension, unstable angina, and/or congestive heart failure requiring hospitalization within the last 6 months
* Transmural myocardial infarction within the last 6 months
* Left ventricular ejection fraction \< 45%
* Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
* Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 calendar days prior to registration
* Hepatic insufficiency resulting in clinical jaundice and/or Coagulation defects
* Acquired Immune Deficiency Syndrome (AIDS) based upon current Centers for Disease Control and Prevention (CDC) definition
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01711658
Study Brief:
Protocol Section:
NCT01711658