Panitumumab Chemoradiotherapy Chemotherapy for Squamous Cancer of the Head and Neck

• There are two parts to this study: Part A and Part B. Participants enrolled in Part A of this study received panitumumab and chemoradiotherapy. Participants enrolled in Part B will receive panitumumab in combination with induction chemotherapy followed by chemoradiotherapy.
• The main purpose of Part A was to examine the safety and the best dosing of panitumumab, chemotherapy and radiation for the treatment of head and neck cancer. The best dosing was determined by increasing doses of chemotherapy given in combination with panitumumab during radiation. The chemotherapy drugs being used in Part A were carboplatin and paclitaxel, which are standard therapies used in head and neck cancer. These drugs were be added to radiation and this combination is called chemoradiotherapy. The investigators have determined the best dose of panitumumab and chemotherapy to give with radiation, Part B has now begun.
• The main purpose of Part B is to examine the safety and best dosing of chemotherapy combined with panitumumab (called induction therapy) prior to receiving panitumumab and chemoradiotherapy. The drugs that are used for induction chemotherapy will be docetaxel, cisplatin and 5-fluorouracil. These drugs are also standard therapies used in head and neck cancer.

Inclusion criteria

• Histologically or cytologically proven squamous cell carcinoma of the head and neck or its variants (such as basaloid squamous cell carcinoma, undifferentiated carcinoma, or adenosquamous cell carcinoma). Primary tumor sites eligible include: nasopharynx, oral cavity, oropharynx, hypopharynx, larynx or unknown primary SCCHN
• Stage III or IV disease, without evidence of distant metastasis, according to American Joint Committee on Cancer
• Measurable disease, according to RECIST.
• No prior chemotherapy, radiotherapy or attempted complete resection of the SCCHN. Diagnostic biopsy, including excisional nodal biopsy and/or tonsillectomy is allowed if the subject has measurable disease at the time of enrollment
• 18 years of age or older
• ECOG Performance Status of 0 or 1
• No active alcohol addiction or other condition that, in the opinion of the study investigators, would interfere with the subject's ability to comply with the treatment plan
• Adequate hepatic and renal function
• Women of childbearing potential must have a negative pregnancy test within 2 weeks of study entry.

Exclusion criteria

• Pregnant or breast feeding women
• Symptomatic peripheral neuropathy of grade 2 or higher by NCI CTCAEv3.0
• Grade 3 or more hearing loss
• History of other malignancy within the previous 5 years, except for nonmelanoma skin cancer, carcinoma in situ of the cervix, bladder or head and neck
• Prior radiation to head and neck
• Other serious illness or medical conditions
• Patients who experienced an involuntary weight loss of more than 20% of their body weight in the 2 months preceding study entry
• Concurrent treatment with any other anticancer therapy
• Prior therapy which affects or targets the ErbB pathway, including any inhibitors of EGFR and ErbB2
• Participation in an investigational drug trial within 30 days of study entry