Boronophenylalanine (BPA)-Based Boron Neutron Capture Therapy (BNCT) in the Treatment Head and Neck Tumors
Head and Neck Cancer
About this trial
This is an interventional treatment trial for Head and Neck Cancer focused on measuring head and neck cancer, boron neutron capture therapy, radiation therapy, boronophenylalanine
Eligibility Criteria
Inclusion Criteria: Histologically confirmed, malignant head and neck cancer. Inoperable tumor, prior surgery may or may not have been done. Prior radiotherapy or chemoradiotherapy has been given. If prior SPECT or PET with 18F-BFA has been done, BPA needs to accumulate at least 2.5 times more in the tumor than in the corresponding contralateral normal tissue. WHO performance status <3. WBC >2,500/mm3, platelets >75,000/mm3, serum creatinine <180 umol/L. A written informed consent. Exclusion Criteria: Lymphoma or other tumor type that is expected to respond to cancer chemotherapy or to a dose of conventional radiation therapy that can be safely given. A non-experimental, effective treatment option is available. Expected survival less than 3 months. Concomitant systemic chemotherapy (prior cancer chemotherapy is allowed). Other concurrent experimental therapy, or such therapy is being planned to be given. Less than 3 months since prior radiation therapy. Untreated or severe, treated congestive heart failure or renal failure. A cardiac pace-maker or an unremovable metal implant present in the head and neck region that will interfere with MRI-based dose-planning. Restlessness or inability to lie in a cast for 30 to 60 minutes. Clinical follow-up after therapy cannot be arranged or the patient is not willing to participate in follow-up. Pregnancy. Age less than 18. The patient is not able to understand the treatment options.
Sites / Locations
- Department of Oncology, Helsinki University Central Hospital
Arms of the Study
Arm 1
Experimental
BNCT.
Boronophenylalanine-based BNCT.