Cancer of Head and Neck
Conditions
Keywords
head and neck squamous cell carcinoma
Brief summary
The study researchers want to look at the overall effects that Metformin may have on the tumor characteristics of Head and Neck cancer cells as well as the interactions that Metformin has on the growth or death of tumor cells.
Detailed description
Subjects will sign informed consent and have their medical records reviewed, a physical exam and blood taken for lab tests and a biopsy of the cancer will be taken to determine eligibility for the study. Following enrollment, the subject will begin to take Metformin at a dosage of 850 mg daily on Days 1 through 3 (in the mornings with breakfast). On day 3 the study team will call to see if the subject is tolerating the Metformin. If tolerated, then the dose will increase to 850 mg twice a day (with breakfast and dinner) on starting on Day 4. This dose is to continue until 24 hours prior to surgery, with a minimum of 14 days but can be extended until 28 days dependent on planned surgery date. The study team will provide the subject with the Metformin and a study diary to record when they take their pills and if there are any issues to communicate to the physician. They will also be contacted by phone or planned visit days to see how their body is tolerating the Metformin throughout their treatment (approximately every 3 days). On Day 14 plus or minus 3 days (or 2 weeks after staring Metformin) and immediately prior to surgery, the physician will collect a blood sample. On the day of surgery, the surgeon will remove the tumor and send it to the lab for evaluation as part of standard cancer care. They will also collect an additional biopsy of the tumor for research purposes to test the effects of Metformin on the tumor cells. The subjects will be followed for 30 days after their surgery. The blood and tumor samples collected will be sent to a research lab at WVU for to test the effect of Metformin, tumor genotype and Metformin genotype interactions on critical tumor cell metabolic parameters and also on anoikis-sensitivity.
Interventions
DRUGMetformin
Sponsors
West Virginia Clinical and Translational Science Institute
West Virginia University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Newly diagnosed HNSCC Stage II-IVB (T1N1-3, T2-3, N0-3, M0) OR Patients with suspected Stage II-IVB tumor as determined by clinical examination or noted via imaging. * Planned complete resection of the primary tumor. * Age \>= 18 years. * ECOG performance status of 0 or 1 * Adequate hepatic, renal, and bone marrow function
Exclusion criteria
* Prior therapy for head and neck cancer * Candidates for neo-adjuvant chemotherapy or chemo-radiation therapy for curative intent. * Co-existing malignancy or malignancies diagnosed within the last 3 years with the exception of basal cell carcinoma or in situ cervical cancer. * History of diabetes mellitus or taking any medications indicated for diabetes mellitus treatment * Contraindication to metformin including hypersensitivity or allergic reaction * Active diagnosis of Alcoholism * Congestive heart failure requiring pharmacologic treatment. * BMI \< 25 * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. * Pregnant or breastfeeding women are excluded from this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tumor cell death estimated by percentage | 30 days |
Countries
United States
Outcome results
None listed