Dose Escalation Study of Hyperbaric Oxygen With Radiation and Chemotherapy to Treat Squamous Cell Carcinoma of the Head and Neck

The goal of this study is to see if patients can tolerate HBO therapy up to five days a week.

Three patients in Arm 1 (HBO on Monday and Friday) will be observed throughout their course of concomitant radiation, chemo and hyperbaric therapy. If these patients appear to tolerate this protocol well, and no adverse effects that can be directly attributed to HBO are observed, then three more patients will be recruited for Arm 2 (HBO on Monday, Wednesday, and Friday). If again these patients appear to tolerate this protocol well, and no adverse effects that can be directly attributed to HBO are observed, then a third group of three patients will be recruited for Arm 3 (HBO Monday through Friday).

If Grade IV acute toxicity is reported for a single patient in any of the arms, 3 more patients will be recruited in the same arm. If no further adverse events occur, the protocol progresses to the next arm. If Grade IV acute toxicity is observed even a single patient, the study will be stopped.

Tumor and/or lymphatic tissue specimens will be obtained prior to starting treatment. Tumor tissue specimens will be analyzed to determine whether there is a predictive susceptibility of tumors to HBO sensitization using currently defined biomarkers known to correlate with survival.

Inclusion criteria

• Patients with histological proof (from the primary lesion and/or lymph nodes) of squamous cell carcinoma of the oral cavity, oropharynx, or hypopharynx.
• Patients should have Stage III or IV disease, M0
• Patients must have life expectancy of at least 6 months and a Karnofsky performance status of ≥ 70
• Age ≥ 18 years and ≤ 70 years
• No distant metastatic disease
• No clinically significant heart disease:
• No significant ventricular arrhythmia requiring medication with antiarrhythmics
• No symptomatic coronary artery disease (angina)
• No myocardial infarction within the last 6 months
• No second or third degree heart block or bundle branch block or clinically significant conduction system abnormality
• Patients must sign a study-specific informed consent form

Exclusion criteria

• Histology other than squamous cell carcinoma
• Evidence of metastasis (below the clavicle or distant) by clinical or radiographic means
• Prior complete resection of the primary tumor
• Prior chemotherapy (Bleomycin) for head and neck cancer or radiotherapy to the head and neck
• Patients with simultaneous primaries
• Pregnancy
• Pulmonary pathologies (risk of decompression-induced pulmonary barotrauma):
• Current, untreated pneumothorax
• Previous history of pneumothorax
• Previous history of intrathoracic surgery
• History of pulmonary blebs or bullous lung disease
• Associated with CO2 retention
• Poorly controlled or associated with acute bronchospasm
• Where the hyperbaric physician deems the patient to have an unacceptable risk for hyperbaric treatments
• Claustrophobia