Tongue Cancer
Conditions
Keywords
Oral Tongue Cancer, Tumor Hypoxia
Brief summary
This is a pilot study in the form of a prospective Phase II, single centre, single arm hypoxia study of oral tongue cancer with FAZA-PET imaging and pimonidazole targeted IHC of surgical specimens.
Detailed description
In head and neck cancer, areas of tumours with low oxygen supply (called tumour hypoxia) harbour cells that are resistant to radiation and are prone to metastasize. Modern radiotherapy techniques are precise enough to deliver radiation to these small areas and could be used to target these areas to receive higher doses of radiation than the rest of the tumour to overcome resistance. Hypoxia can be seen in the body using special imaging such as \[F-18\]-FAZA-PET (\[F-18\]-Fluoroazomycin arabinoside positron emission tomography) but it has not been tested as a method for creating radiation treatment targets. As part of regular pathology tumour tissue is sliced extremely thinly (\<1/100th of a millimeter) and stained so that individual cells can be seen under a microscope. Immunohistochemistry (IHC) is a special type of stain that can specifically highlight hypoxic areas. This method is considered the most accurate way to inspect for the presence of hypoxia. There is not a specific staining target for hypoxia ordinarily, but when patients ingest a substance called pimonidazole hydrochloride (HCl) it builds up specifically in hypoxic areas and can be targeted for IHC staining. In this study participants with oral tongue cancer will have a \[F-18\]-FAZA-PET scan and take a single dose of oral pimonidazole-HCl before having surgery to remove their cancer. The whole tumour will be used to create microscope slides using very thin slices of the tumour. The slices will be stained using IHC to show where the pimonidazole has built up and digital scans of the slides will be made. The hypoxia seen on the FAZA-PET scan will be matched with hypoxia on the electronic slides to see if the FAZA truly shows where hypoxia is in tumours and if it could be used as a way to plan radiation treatments to deliver more radiation to just those areas.
Interventions
RADIATION(18)F-Fluoroazomycin arabinoside
FAZA PET diagnostic testing
DRUGPimonidazole
oral pimonidazole hypoxia labeling
Sponsors
Sunnybrook Research Institute
University of Toronto
Sunnybrook Health Sciences Centre
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Biopsy proven Stage II-III oral tongue squamous cell carcinoma * Naïve to treatment for resectable disease * Surgical resection as definitive treatment modality * Ability to participate and willingness to give written informed consent prior to performance of any study-related procedures and to comply with the study protocol * Adequate hematologic, renal and liver function as defined by the following laboratory values up to 30 days prior to commencement of dosing (administration of FAZA): * Absolute neutrophil count (ANC) ≥ 1.5 x 109/L * Platelet count ≥ 50 ×109/L * Hemoglobin ≥ 9 g/dL * Bilirubin ≤ 1.5 × upper limit of normal (ULN) (20.0 µmol) * Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), and alkaline phosphatase ≤ 2.5 × the ULN (37 U/L, 40 U/L, 120 U/L) * Serum creatinine ≤ 1.5 × the ULN (106 µmol/L) or creatinine clearance ≥ 50 mL/min on the basis of the Cockroft-Gault glomerular filtration rate estimation: \[(140-age) × (weight in kg × (0.85 if female)\]/\[72 × (serum creatinine in mg/dL)\] * Prothrombin time (PT), international normalized ratio (INR), partial thromboblastin time (PTT) ≤ 1.5 × the ULN (respectively 1.1, 14 sec, 35 sec) * Negative serum pregnancy test within 14 days prior to commencement of dosing in women of childbearing potential. Women of non-childbearing potential need not undergo pregnancy testing. Female participants of childbearing potential agree to use adequate methods of contraception from the time of enrollment until 28 days after surgery. Clinically acceptable methods of birth control for this study include intrauterine devices (IUD), birth control pills, hormonal implants, injectable contraceptives, and using barrier methods such as condoms, vaginal diaphragm with spermicide, or sponge.
Exclusion criteria
* Patients who have received prior chemotherapy or radiation therapy for their oral tongue carcinoma * Stage I, Stage III T1/N1/M0, and Stage IV disease * Pregnant or breastfeeding at the time of consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cellular hypoxia correlation | 1 year | The degree to which hypoxic signal measured by FAZA-PET imaging is correlated with true cellular hypoxia confirmed by immunohistochemical staining of pimonidazole using a 3D whole-mount approach |
| Hypoxic reference standard | 1 year | A reference standard hypoxic radiation target will be defined through the correlation of functional F18-FAZA PET imaging to a pimonidazole-stained 3D whole mounted histological specimen. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Registration quality | 1 year | The quality of registration will be assessed through measuring registration error of various automatic and semi-automatic co-registration techniques |
| Textural feature comparison | 1 year | Potential relationships between textural features of MRI, PET-CT, and immunohistochemistry will be evaluated. |
Countries
Canada
Outcome results
None listed