Metformin Hydrochloride and Doxycycline in Treating Patients With Head and Neck Squamous Cell Carcinoma That Can Be Removed by Surgery
- Conditions
- PharynxLarynxLIPOral Cavity
- Interventions
- Registration Number
- NCT03076281
- Brief Summary
This randomized phase II trial studies how well metformin hydrochloride and doxycycline work in treating patients with head and neck squamous cell carcinoma that can be removed by surgery. Metformin hydrochloride may reduce the metabolic activity of cancer cells and of surrounding supportive tissue. Doxycycline may minimize toxic side effects of anti-cancer therapy. Giving metformin hydrochloride and doxycycline may work better in treating patients with head and neck squamous cell carcinoma.
- Detailed Description
PRIMARY OBJECTIVES:
I. To determine if treatment with metformin hydrochloride (metformin), doxycycline, or a combination of metformin and doxycycline can increase the percentage of stromal cells that express CAV1 in patients with squamous cell carcinoma of the head and neck.
SECONDARY OBJECTIVES:
I. To determine the effect of metformin, doxycycline, or metformin and doxycycline treatment on the percentage of tumor cells that are apoptotic as determined by the TdT-Mediated dUTP Nick End Labeling Assay (TUNEL) assay, and express MCT4, MCT1, BGAL, and TOMM20 in squamous carcinoma of head and neck region tumor cells.
II. To assess safety and tolerability of metformin, doxycycline, or metformin and doxycycline treatment in subjects with squamous cell carcinoma of the head and neck.
TERTIARY OBJECTIVES:
I. To assess the effect of metformin, doxycycline, or metformin and doxycycline therapy on the metabolic profile of cancer cells and stroma using mass spectroscopy imaging (MSI) on paired samples, comparing metabolite profiles in the pre-treatment and post-treatment tumor samples.
II. To assess the effect of metformin, doxycycline, or metformin and doxycycline therapy on the metabolic state of the patient as characterized serologically by: erythrocyte sedimentation rate, exosome evaluation, metabolomics profile, and micro ribonucleic acid (RNA) expression profiles and physiologically by performing a nutritional assessment via a nutritionist-mediated 3-day dietary recall and comparing a patient's estimated dietary intake against their estimated caloric needs.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 7
- Diagnosis of head and neck squamous cell carcinoma that is either biopsy proven or suspected based on history, physical, and or radiographic findings, and who are planned for definitive resection of the tumor without the use of neoadjuvant chemotherapy or radiation therapy at TJUH are eligible to participate.
- Subjects must be ≥ 18 years of age at time of consent.
- Patient must be able to swallow pills.
- Patients with serum creatinine levels less than 1.5 mg/dL
- Women of childbearing potential must have a negative urine or blood pregnancy test within 14 days of study enrollment.
- Informed Consent: All subjects must be able to comprehend and sign a written informed consent document.
- ECOG Performance status ≤1
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Subjects that do not have a baseline tumor specimen/biopsy prior to starting study medications.
a. Tumor specimens do not need to be at Jefferson at time of eligibility determination. Tumor specimens held at outside institutions should be requested for analysis of pre-treatment tumor vs post-treatment tumor.
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Subjects who are pregnant or breastfeeding, or may become pregnant during metformin and doxycycline administration.
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Received prior cancer therapy for the HNSCC that is being resected.
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Subjects on metformin or doxycycline for any reason during the preceding 4 weeks.
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Diabetic subjects that are managed by taking metformin or insulin
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Subjects who have received iodinated contrast dye must wait 12 hours prior to starting Metformin. If a CT scan with contrast is scheduled after screening and consent, the metformin cannot be taken until after the CT with contrast has been completed and they have waited 12 hours.
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Patients with serum creatine ≥1.5 mg/dL
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Patients with history of lactic or any other metabolic acidosis.
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Patients with history of congestive heart failure stage III or greater.
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Patients scheduled for definitive cancer surgical resection less than 7 days from beginning of study drug administration or greater than 6 weeks from beginning study drug administration.
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Patients with history of hepatic dysfunction or hepatic disease and abnormal liver function tests defined as AST, ALT, Alk Phos, and or total bilirubin greater than 2.5 times the upper limit of normal. Patients who have a history of hepatic dysfunction or hepatic disease and normal liver function tests will be eligible to participate.
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Patients with a current history (in the past 30 days) of heavy drinking which is defined in accordance with CDC definition as more than 8 drinks per week for women and more than 15 drinks per week for men. A standard drink contains .6 ounces of pure alcohol. Generally, this amount of pure alcohol is found in 12-ounces of beer, 8-ounces of malt liquor, 5-ounces of wine, 1.5-ounces or a "shot" of 80-proof distilled spirits or liquor (e.g., gin, rum, vodka, or whiskey). While on study, patients should limit their alcohol consumption to no more than 8 drinks per week for women and no more than 15 drinks per week for men.
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Patient with prior allergic reaction to metformin, doxycycline, or any other tetracycline antibiotic in the past.
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Patient is on medications that are contraindicated with metformin or doxycycline under current FDA recommendations. The following is a list of medications identified as class D (consider therapy modification) when treatment with metformin or doxycycline is considered:
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Class D:
- Bismuth Subsalicylate
- Cimetidine
- Iodinated cont
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Arm C (metformin hydrochloride, doxycycline) Metformin +Doxycycline Patients receive metformin hydrochloride PO daily on days 1-3 and twice daily starting on day 4 to the day prior to surgery and doxycycline PO every 12 hours on days 1to the day prior to surgery in the absence of disease progression or unacceptable toxicity. Arm A (metformin hydrochloride) Metformin Hydrochloride Patients receive metformin hydrochloride PO daily on days 1-3 and twice daily starting on day 4 to the day prior to surgery in the absence of disease progression or unacceptable toxicity Arm B (doxycycline) Doxycycline Patients receive doxycycline PO every 12 hours on days 1 to the day prior to surgery in the absence of disease progression or unacceptable toxicity.
- Primary Outcome Measures
Name Time Method Change in percent of CFS expressing CAV-1 at an intensity of 1+ or greater assessed in tumor-associated stroma cells by immunohistochemistry (IHC) Baseline to 30 days after last drug dose Within-patient change in IHC scores will be analyzed using the Wilcoxon signed-rank test. Comparisons will be made between pretreatment and post-treatment within each of the cohorts
- Secondary Outcome Measures
Name Time Method Incidence of adverse events as assessed by National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0 Up to 30 days after last drug dose Safety will be provided in descriptive tables.
Change in percent of tumor cells expressing MCT4, that are TUNEL positive and that express MCT1 Baseline to 30 days after last drug dose Analysis will be performed using the Wilcoxon signed-rank test.
Change in percent of tumor cells expressing MCT4, that are TUNEL positive and that express BGAL Baseline to 30 days after last drug dose Analysis will be performed using the Wilcoxon signed-rank test.
Change in percent of tumor cells expressing MCT4, that are TUNEL positive and that express MCT4 Baseline to 30 days after last drug dose Analysis will be performed using the Wilcoxon signed-rank test.
Change in percent of tumor cells expressing MCT4, that are TUNEL positive and that express TOMM20 Baseline to 30 days after last drug dose Analysis will be performed using the Wilcoxon signed-rank test.
Trial Locations
- Locations (1)
Sidney Kimmel Cancer Center at Thomas Jefferson University
🇺🇸Philadelphia, Pennsylvania, United States