Head and Neck Cancer Clinical Trial
Official title:
A Phase II Trial of Daily Bolus Flavopiridol for Five Consecutive Days in Patients With Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck (SCCHN)
RATIONALE: Drugs used in chemotherapy work in different ways to stop tumor cells from
dividing so they stop growing or die.
PURPOSE: Phase II trial to study the effectiveness of flavopiridol in treating patients who
have recurrent or metastatic head and neck cancer.
OBJECTIVES:
- Determine the standard response rate (complete response and partial response) and
duration of response in patients with recurrent or metastatic squamous cell carcinoma
of the head and neck treated with flavopiridol.
- Determine the qualitative and quantitative toxic effects of this regimen in these
patients.
- Determine the progression-free and overall survival of patients treated with this
regimen.
- Determine the effects of anti-platelet agents, aspirin and clopidogrel bisulfate, on
the pharmacology of flavopiridol in these patients.
- Determine the effects of prophylactic anticoagulation with anti-platelet agents,
aspirin and clopidogrel bisulfate, on the incidence of flavopiridol-related thrombosis
in these patients.
OUTLINE: Patients receive flavopiridol IV over 1 hour on days 1-5. Courses repeat every 3
weeks in the absence of disease progression or unacceptable toxicity.
Patients also receive oral aspirin and clopidogrel bisulfate beginning on day 0 and
continuing throughout the study.
Patients are followed until death.
PROJECTED ACCRUAL: A total of 12-37 patients will be accrued for this study within 1-3
years.
;
Primary Purpose: Treatment
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