Rapamycin Therapy in Head and Neck Squamous Cell Carcinoma

Completed · Phase 1/Phase 2

Conditions studied: Mouth Neoplasms, Head and Neck Neoplasms, Tongue Neoplasms, Carcinoma, Squamous Cell

In brief

Background: \- Advanced-stage head and neck cancer (head and neck squamous cell carcinoma \[HNSCC\]) has moderately successful treatment outcomes, usually involving surgery as part of the standard treatment. Researchers are investigating the use of the drug rapamycin to prevent tumor growth in HNSCC, and are interested in using it to treat individuals with HNSCC that has not been treated previously with other drugs, radiation, or surgery. Objectives: \- To evaluate the usefulness of rapamycin in decreasing tumor size prior to surgery for head and neck squamous cell carcinoma. Eligibility: \- Individuals at least 18 years of age who have been diagnosed with advanced head and neck squamous cell carcinoma that has not yet been treated. Design: * Participants will be screened with a physical examination, medical history, blood tests, and imaging studies. * Approximately 1 month before scheduled surgery, participants will begin to receive rapamycin. Participants will take rapamycin once daily for 21 days, followed by a 7-day period without the drug. * During the 21-day rapamycin treatment, participants will have weekly study visits to provide blood and urine samples and have possible tumor biopsies and imaging studies such as x-rays or tumor photographs. Participants will have additional study visits for tests 1 day and 1 week after the end of rapamycin treatment, followed by HNSCC surgery. * Participants will have a final visit to provide blood samples 30 days after surgery. * Participants medical records will be reviewed 1 year after surgery; however, participants will not need to have further study visits at this time.

Key facts

Study ID

NCT01195922

Run by

National Institute of Dental and Craniofacial Research (NIDCR)

People needed

37

Starts

2010-08-01

Expected to finish

2015-12-01

Last updated by the study team

2017-12-06

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants must meet all of the following inclusion criteria:
• Age 18 years and older
• Histologically confirmed previously untreated squamous cell carcinoma o f the oral cavity or oropharynx accessible for biopsy
• Clinical stage II, III, or IVA disease without distant metastasis, as defined by the American Joint Committee on Cancer Staging System, Seventh edition.
• Definitive therapy to include surgical resection or chemoradiation for curative purposes
• Life expectancy o f greater than 6 months
• Eastern Cooperative Oncology Group ( ECOG) performance status of 0 or 1
• Willing and able to provide written informed consent

You may not qualify if…

• Participants who meet any of the following criteria are not eligible for enrollment:
• Surgical resection or chemoradiation of the HNSCC is contraindicated
• Prior head or neck squamous cell carcinoma within 5 years, except for previously treated skin cancer
• Received chemotherapy targeted monoclonal antibody therapy or investigational therapy within 30 days prior to enrollment
• Previous radiation therapy to the head or neck
• No measurable tumor remaining after prior biopsy or negative margins from prior biopsy
• Inadequate hematologic, renal or liver function within l4 days prior to the first rapamycin dosing visit, as defined by:
• Absolute neutrophil count less than 1.5 times 10 (9)/L
• CD4 count < 400 (to account for natural fluctuations in CD4 levels, participants with at least one CD4 count (Bullet) 400 within 14 days prior to dosing will not be excluded)
• Platelet count less than 100 times 10(9)/L
• Hemoglobin less than l0 g/dL (eligibility level for hemoglobin may be reached by transfusion)
• AST, ALT or bilirubin greater than 1.5 times the upper limit of local lab normal values
• Total cholesterol level greater than 350 mg/dL
• Triglyceride level greater than 400 mg/dL
• International Normalized Ratio (INR) greater than 1.5
• Serum creatinine greater than 1.5mg/dL
• Active hepatitis or HBV or HCV infection
• Women who are pregnant or lactating (female of child-bearing age must be abstinent or use a barrier type birth control method throughout the study)
• Presence of any contraindications to rapamycin therapy, including HlV-protease inhibitors and drugs or agents that are modulators of cytochrome P-450 3A4 (CYP3A4) and p-glycoprotein(P-gp)
• Hypersensitivity to rapamycin
• 11 .Has received live vaccine (such as influenza nasal vaccine measles mumps, rubella, oral polio, B CG, yellow fever, varicella, or TY2la typhoid) in the past 30 days or has plans to take a live vaccine in the next 3 months
• Any cognitive impairment that limits the subject s or the subject s legally authorized representative s ability to understand the protocol, provide informed consent or assent, or to comply with the protocol procedures
• Unable or unwilling to comply with the requirements of the protocol

Where it is running

• National Institutes of Health Clinical Center, 9000 Rockville Pike — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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