Pilot Study of Metformin in Head and Neck Squamous Cell Cancer and Its Effects on Stromal-epithelial Metabolic Uncoupling

Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University (Other)
Overall Status
Completed
CT.gov ID
NCT02083692
Collaborator
(none)
50
1
1

Study Details

Study Description

Brief Summary

The purpose of this study is to assess the effect of metformin in tumor metabolism in patients with head and neck cancer by evaluating metformin's ability to decrease TOMM20 expression in squamous carcinoma cells and decrease MCT4 expression in fibroblasts.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Pilot Study of Metformin in Head and Neck Squamous Cell Cancer and Its Effects on Stromal-epithelial Metabolic Uncoupling.
Study Start Date :
Sep 1, 2013
Actual Primary Completion Date :
May 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Metformin

Drug: Metformin

Outcome Measures

Primary Outcome Measures

  1. Change in TOMM20 and MCT4 expression from tumor cells from date of biopsy and date of surgery [date of biopsy and date of surgery (9-28 days)]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of head and neck cancer biopsy proven, and who have a scheduled appointment for definitive resection of the tumor at TJUH

  • Age ≥ 18 years of age and ≤80 years old.

  • Newly diagnosed with HNSCC cancer.

  • No prior therapy for HNSCC cancer is permitted for enrollment in the trial.

  • All subjects must be able to comprehend and sign a written informed consent document.

Exclusion Criteria:
  • Pregnant or may become pregnant during metformin administration.

  • On metformin for any reason during the preceding 4 weeks.

  • Diabetic patients are eligible if they are not taking metformin, insulin or sulfonylureas.

  • Received iodinated contrast dye less than 48 hours prior to screening meet a temporary exclusion criteria to receive metformin. These patients cannot start investigational metformin until 48 hours have elapsed from contrast administration. Subjects who are scheduled for iodinated contrast dye administration within 48 hours of definitive surgery are excluded.

  • Plasma alanine aminotransferase greater than 40 IU/dL.

  • Plasma aspartate aminotransferase greater than 45 IU/dL.

  • Plasma creatinine level greater than 1.3 mg/dL.

  • Plasma alkaline phosphatase greater than 190 IU/dL.

  • Plasma bicarbonate less than 22 mEq/L or history of lactic or any other metabolic acidosis.

  • History of congestive heart failure.

  • Myocardial ischemia or peripheral muscle ischemia.

  • Sepsis or severe infection.

  • History of lung disease currently requiring any pharmacologic or supplemental oxygen treatment.

  • Scheduled for definitive HNSCC cancer surgical resection less than two weeks from enrollment or greater than five weeks from enrollment.

  • History of hepatic dysfunction or hepatic disease.

  • Excessive alcohol intake which is defined in accordance with CDC definitions as more than 1 drink per day for women and more than 2 drinks per day for men.

All medications are permitted except those that are contraindicated with metformin under current FDA recommendations.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Thomas Jefferson University Philadelphia Pennsylvania United States 19107

Sponsors and Collaborators

  • Sidney Kimmel Cancer Center at Thomas Jefferson University

Investigators

  • Principal Investigator: Joseph Curry, MD, Thomas Jefferson University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Sidney Kimmel Cancer Center at Thomas Jefferson University
ClinicalTrials.gov Identifier:
NCT02083692
Other Study ID Numbers:
  • 13D.458
First Posted:
Mar 11, 2014
Last Update Posted:
Oct 19, 2016
Last Verified:
Oct 1, 2016

Study Results

No Results Posted as of Oct 19, 2016