Stage IV Melanoma Clinical Trial
Official title:
A Phase II Study of BAY 43-9006 (NSC 724772) in Unresectable Stage III and IV Melanoma (IND 69,869)
Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. This phase II trial is studying how well sorafenib works in treating patients with stage III or stage IV melanoma that cannot be removed by surgery
PRIMARY OBJECTIVES:
I. Determine the efficacy of sorafenib, in terms of anti-tumor effects and proportion of
clinical responses, in patients with previously untreated unresectable stage III or stage IV
melanoma.
SECONDARY OBJECTIVES:
I. Correlate the efficacy of this drug with the presence of mutant or wild-type BRAF gene in
tumors of these patients.
II. Determine the toxicity profile of this drug in these patients. III. Correlate serum
cryptic collagen epitopes with the extent of tumor burden, invasion, and metastasis in
patients treated with this drug.
IV. Determine the potential of serum cryptic collagen epitopes to serve as a surrogate
marker for monitoring the course of disease in patients treated with this drug.
OUTLINE: This is a multicenter study. Patients are stratified according to presence of BRAF
gene mutation in tumor sample (yes vs no).
Patients receive oral sorafenib twice daily on days 1-28. Courses repeat every 28 days in
the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed annually.
PROJECTED ACCRUAL: A total of 26-74 patients (13-37 per stratum) will be accrued for this
study within 5.2-18.5 months.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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