Finding studies
Finding studies
Take this into the appointment.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Lead
M.D. Anderson Cancer Center
With
OBJECTIVES: Primary * Determine the antiangiogenic effects of PEG-interferon alfa-2b, in terms of pre- and post-treatment levels of microvessel density (MVD), endothelial cell apoptosis, vascular endothelial growth factor (VEGF), interleukin-8, basic fibroblast growth factor (bFGF), Nuclear Factor-KappaB (NF-KB), matrix metalloproteinase/MMP-9, and NF-KB in biopsy specimens, from patients with resectable stage II-IV squamous cell carcinoma of the head and neck. Secondary * Determine the toxicity profile of this drug in these patients. * Determine the clinical response in patients treated with this drug. OUTLINE: This is a randomized, controlled study. Patients are randomized to 1 of 4 treatment arms. * Arm I: Patients undergo surgery within 3 weeks after randomization. * Arm II: Patients receive PEG-interferon alfa-2b subcutaneously on days 1, 8, and 15. * Arm III: Patients receive PEG-interferon alfa-2b as in arm II but at a higher dose. * Arm IV: Patients receive PEG-interferon alfa-2b as in arm II but at a higher dose than in arm III. In arms II, III, and IV, patients undergo surgery within 1 week after completion of PEG-interferon alfa-2b. After completion of study treatment, patients are followed for up to 30 days. PROJECTED ACCRUAL: A maximum of 72 patients will be accrued for this study.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
