Imatinib Mesylate (Gleevec) and Docetaxel in Patients With Head and Neck Squamous Cell Cancer - Full Text View

Sponsor:	M.D. Anderson Cancer Center
Collaborator:	Novartis
Information provided by:	M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:	NCT00485485

Purpose

Primary Objective:

To determine the efficacy of the combination of imatinib mesylate and docetaxel in recurrent or metastatic head and neck squamous cell cancer by serial measurements of tumor response (extent, frequency, duration).

Secondary Objectives:

To assess the safety and tolerability of imatinib mesylate and docetaxel in patients with recurrent or metastatic head and neck squamous cell cancer.
To explore the biologic effects of imatinib mesylate and docetaxel on tumor tissue by immunohistochemical analysis of microvessel density and phosphorylation of PDGF-R.
To explore the effects of imatinib mesylate and docetaxel on surrogate markers in serum.
To assess the rate of survival.

Condition	Intervention	Phase
Head and Neck Cancer Squamous Cell Cancer	Drug: Imatinib Mesylate Drug: Docetaxel	Phase II

Study Type:	Interventional
Study Design:	Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Official Title:	Phase II Study of Imatinib Mesylate and Docetaxel in Patients With Metastatic or Recurrent Head and Neck Squamous Cell Cancer

Resource links provided by NLM:

MedlinePlus related topics: Cancer Head and Neck Cancer

Drug Information available for: Docetaxel Imatinib Imatinib mesylate

U.S. FDA Resources

Further study details as provided by M.D. Anderson Cancer Center:

Primary Outcome Measures:

To learn if Gleevec® (imatinib mesylate) given with Taxotere® (docetaxel) can help to control head and neck squamous cell cancer that has spread or reappeared. [ Time Frame: 29 Months ] [ Designated as safety issue: Yes ]

Estimated Enrollment:	58
Study Start Date:	January 2007
Estimated Study Completion Date:	June 2009
Estimated Primary Completion Date:	June 2009 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
1: Experimental Imatinib Mesylate + Docetaxel	Drug: Imatinib Mesylate 400 mg PO Daily Drug: Docetaxel 60 mg/m^2 IV Over 1 Hour Every 3 Weeks

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Detailed Description:

Imatinib mesylate is designed to block certain proteins important in the growth of cancer. Docetaxel is designed to target and destroy cancer cells.

Before you can start treatment on this study, you will have "screening tests." These tests will help the doctor decide if you are eligible to take part in the study. You will have your complete medical history recorded and a physical exam, including measurement of your vital signs (pulse rate, blood pressure, and body temperature) and weight. You will be asked about any medications you are taking and about your alcohol and/or tobacco use. You will have a performance status evaluation (a test looking at your ability to perform day-to-day activities). Blood (about 3 teaspoons) will be drawn for routine tests, including a pregnancy test for women who are able to have children. The pregnancy test must be negative. You will have a chest x-ray and a CT or magnetic resonance imaging (MRI) scan to measure the size of the tumor in your body. If there is not already a tumor tissue sample that can be evaluated, you will have a tumor biopsy before treatment. Depending on where the tumor is located, you will either have a small amount of tissue removed using a needle or by surgery.

If you are found to be eligible to take part in this study, you will take 4 imatinib mesylate tablets by mouth once a day with a meal and a large glass of water (about 8-10 ounces.) A treatment cycle on this study is 21 days. You should keep normal eating habits, however a low-fat breakfast is recommended (for example, a light continental breakfast of toast and juice). Foods and drinks containing caffeine or grapefruit should be avoided. You should wait at least 1 hour after taking the last tablet before going to bed. If vomiting occurs, do not take any extra study medication.

You will be given a patient diary to record when you take your medication. You should bring the diary to each clinic visit, and the study nurse will review it each time.

Docetaxel will be given through a vein in your arm on the first day of each 21-day treatment cycle for a total of 6 cycles. The infusion will take 1 hour.

You will need to take steroids (dexamethasone) before receiving docetaxel to try to prevent fluid accumulation and allergic reactions. You will take dexamethasone by mouth twice a day on the day before the docetaxel infusion, the day of the infusion, and the day after infusion. You will receive an extra dose of dexamethasone (either through a needle in a vein or by mouth) on the day of infusion of the chemotherapy either through a needle in a vein or by mouth.

Every 3 weeks while on this study, you will have a physical exam, including measurement of your vital signs and weight, and a performance status evaluation. During the first 4 weeks, blood (about 3 teaspoons each time) will be drawn once a week for routine tests. After that, blood (about 3 teaspoons each time) will be drawn once at Week 5, once at Week 7, and then every 3 weeks after that. In addition, your tumor will be measured by a CT or MRI scan every 6 weeks (at Weeks 7, 13, and 19).

If you develop any intolerable symptoms or certain changes in your blood tests, your treatment may be delayed and/or the dose may be decreased until the symptoms are gone. It may even be necessary to stop your treatment. You will be informed of any changes in your dosing schedule or in the doses of your medication after your doctor evaluates you in the clinic.

You may receive up to 6 cycles of the study treatment. Your continued participation in this study depends on how the cancer responds to the study drugs. Your doctor may decide to take you off this study if you experience intolerable side effects or the medical condition gets worse.

After you have completed all of your treatment, you will have an end-of-study visit. At this visit you will have a physical exam, including measurement of your vital signs and weight. You will have a performance status evaluation. You will have blood (about 3-4 teaspoons) drawn for routine tests. Your tumor will be measured by a CT or MRI scan.

This is an investigational study. Imatinib mesylate is FDA approved and docetaxel are FDA approved for other types of cancer however their use together in this study is investigational. Dexamethasone is required to be given with docetaxel. All three drugs are commercially available. Up to 58 patients will take part in this study. All will be enrolled at M. D. Anderson.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

A written, voluntary informed consent form must be completed prior to beginning any study procedure.
Patients >/= 18 years of age.
Histologically documented diagnosis of head and neck squamous cell cancer
At least one measurable site of disease and can be assessed by RECIST.
Performance status 0-2 (ECOG)
Patients must have adequate hepatic, renal, and bone marrow function, defined as the following: (1) total bilirubin < 1.5 x ULN; (2) SGOT and SGPT < 2.5 x UNL; (3) creatinine < 1.5 x ULN; (4) ANC > 1.5 x 10^9/L; (5) platelets > 100 x 10^9/L.
Female patients of childbearing potential must have negative pregnancy test within 7 days before initiation of study drug dosing. Postmenopausal women must be amenorrheic for at least 12 months to be considered of non-childbearing potential. Male and female patients of reproductive potential must agree to employ an effective barrier method of birth control (i.e. condoms, diaphragm) throughout the study and for up to 3 months following discontinuation of study drug.
Patients who have not been treated for recurrent or metastatic HNSCC (i.e. Patients who have been treated with chemotherapy for induction/adjuvant or concurrent therapy with radiation in the setting of definitive treatment but have now developed recurrent or metastatic disease are eligible).

Exclusion Criteria:

Prior exposure to docetaxel or imatinib mesylate.
Patient has received any other investigational agents within 30 days of first day of study drug dosing.
Patients with myocardial infarction within the past 6 months or New York Heart Association class 3 or 4 congestive heart failure.
Female patients who are pregnant or breast-feeding.
Patient has a severe and/or uncontrolled medical disease (i.e., uncontrolled diabetes, chronic renal disease, or active uncontrolled infection (i.e. septic).
Patient has unstable brain metastasis. Unstable brain metastasis is defined as patients on steroid medication to control symptoms or patient with motor neurologic compromise due to brain metastasis. Patients with treated brain metastasis are eligible if they are > 6 weeks out from therapy and off all steroid medication.
Patient has known chronic liver disease (i.e., chronic active hepatitis or cirrhosis).
Patient has a known diagnosis of human immunodeficiency virus (HIV) infection. HIV patients are at much greater risk of infection when receiving highly myelosuppressive agents (docetaxel and imatinib) and for safety reasons are not eligible for this trial.
Patient received chemotherapy within 4 weeks (6 weeks for nitrosourea or mitomycin-C) prior to study entry, unless the disease is rapidly progressing.
Patient previously received radiotherapy to >/= 25 % of the bone marrow
Patient had a major surgery within 2 weeks prior to study entry.
Patient with any significant history of non-compliance to medical regimens or with inability to grant reliable informed consent.
Patients must agree not to use herbal remedies or other over-the-counter biologics (i.e. shark cartilage)
History of hypersensitivity to docetaxel or other taxane therapy.
History of severe hypersensitivity reaction to drugs formulated with polysorbate 80.
Patients taking therapeutic levels of warfarin. However, patients receiving 1 mg daily for catheter related anticoagulation are eligible for the study.
Prior pericardial effusion requiring intervention such as pericardiocentesis or pericardial window within 2 months of study entry.
Patient is < 5 years free of another primary malignancy except: if the other primary malignancy is not currently clinically significant nor requiring active intervention, or if other primary malignancy is a basal cell skin cancer or a cervical carcinoma in situ. Existence of any other malignant disease is not allowed.
Patients with a history of Regional Ileitis, Colitis, or Crohn's disease, or any other relevant medical history related to the integrity of the bowel wall as there may be an increased risk of bowel perforation with the combination of Docetaxel and Imatinib.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00485485

Locations

United States, Texas
U.T.M.D. Anderson Cancer Center
Houston, Texas, United States, 77030

Sponsors and Collaborators

M.D. Anderson Cancer Center

Novartis

Investigators

Principal Investigator:

Anne S. Tsao, MD

U.T.M.D. Anderson Cancer Center

More Information

Additional Information:

UT MD Anderson Cancer Center This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	U.T.M.D. Anderson Cancer Center ( Anne S. Tsao, MD/Assistant Professor )
Study ID Numbers:	2006-0362
Study First Received:	June 12, 2007
Last Updated:	January 8, 2009
ClinicalTrials.gov Identifier:	NCT00485485 History of Changes
Health Authority:	United States: Institutional Review Board

Keywords provided by M.D. Anderson Cancer Center:

Head and Neck Cancer
Squamous Cell Cancer
Imatinib Mesylate
Gleevec

Imatinib
STI571
Docetaxel
Taxotere

Additional relevant MeSH terms:

Neoplasms by Histologic Type
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Enzyme Inhibitors
Protein Kinase Inhibitors
Pharmacologic Actions
Carcinoma
Docetaxel

Imatinib
Neoplasms
Neoplasms by Site
Head and Neck Neoplasms
Therapeutic Uses
Neoplasms, Squamous Cell
Carcinoma, Squamous Cell
Neoplasms, Glandular and Epithelial

ClinicalTrials.gov processed this record on November 25, 2009