Bevacizumab/Tarceva and Tarceva/Sulindac in Squamous Cell Carcinoma of the Head and Neck

Stopped early · Phase 2

Conditions studied: Squamous Cell Carcinoma of the Head and Neck (SCCHN)

In brief

The main purpose of this research study is to collect information to learn how effective erlotinib (tarceva) is in combination with either bevacizumab or sulindac in treating patients with squamous cell carcinoma of the head and neck. Erlotinib and bevacizumab are targeted therapy drugs that can control tumor growth by targeting specific abnormalities sometimes found on cancer cells. Erlotinib targets epidermal growth factor receptor (EGFR), and bevacizumab targets vascular endothelial growth factor (VEGF). Sulindac is a non-steroidal anti-inflammatory drug (NSAID) that can block G protein-coupled receptor which laboratory evidence shows is associated with both cancer cell growth and EGFR activity. The bevacizumab being administered in this study is not a commercially marketed formulation of the drug. Previous research with head and neck cancer suggest that erlotinib alone has some anti-cancer activity. This research study is designed to see how well erlotinib works in combination with bevacizumab or sulindac in head and neck cancer.

Key facts

Study ID

NCT00392665

Run by

Massachusetts General Hospital

People needed

36

Starts

2006-10-01

Expected to finish

2013-12-01

Last updated by the study team

2017-04-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically/cytologically documented SCCHN, excluding salivary gland primary sites
• 18 years of age or older
• Have evaluable locoregional and/or metastatic disease according to RECIST that is not appropriate for treatment by primary surgical resection or radiotherapy
• Have locoregional and/or metastatic disease that has failed to respond to or relapsed from at least one prior chemotherapy or chemoradiotherapy
• Life expectancy of at least 4 months
• ECOG performance status of 0-2
• Use of effective means of contraception in patients of child-bearing potential

You may not qualify if…

• Other malignancy within 5 years except non-melanomatous skin cancer, or carcinoma in situ of the cervix, bladder or head and neck
• Concurrent anticancer therapy other than that of this study
• Treatment with any anticancer drug within 28 days of day 1
• Radiotherapy within 28 days of day 1
• Any unresolved toxicity greater than NCI-CTCAE v 3.0 grade 2 from prior systemic anticancer therapy
• Any prior therapy that targets the ErbB and/or VEGF pathways
• Concurrent therapy with any NSAID
• Known hypersensitivity characterized by acute bronchospasm, urticaria and/or rhinitis to NSAIDs, including aspirin
• Serum creatinine > 1.5 x ULN
• Abnormal LFTs as outlined in protocol
• Blood pressure > 150/100mmHg
• Active unstable angina, or myocardial infarction within 6 months
• NYHA Grade II or greater congestive heart failure
• History of stroke within 6 months
• Clinically significant active peripheral vascular disease
• Absolute neutrophil count < 1000/mm3 or platelets < 100,000/mm3
• Evidence of bleeding diathesis or coagulopathy.
• Tumor encasing the carotid artery, or other major vessel that in the opinion of the investigators is at risk for tumor-related hemorrhage
• Presence of central nervous system or brain metastases
• Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 1, or anticipation of need for major surgical procedure during the course of the study
• Minor surgical procedures such as fine needle aspiration or core biopsy within 5 days prior to day 1
• Pregnant or lactating
• History of abdominal fistula or intra-abdominal abscess within 6 months
• History of gastrointestinal ulcer, perforation, or bleeding within 6 months
• Serious non-healing wound or ulcer or active uncontrolled infection

Where it is running

• Massachusetts General Hospital — Boston, Massachusetts, United States
• Dana-Farber Cancer Institute — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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