RATIONALE: Thalidomide may stop the growth of melanoma by blocking blood flow to the tumor. It may also stimulate the immune system in different ways and stop tumor cells from growing. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving thalidomide together with temozolomide may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving thalidomide together with temozolomide works in treating patients with stage IV melanoma that cannot be removed by surgery.
OBJECTIVES: * Determine the 6-month progression-free survival of patients with unresectable stage IV malignant cutaneous melanoma treated with thalidomide and temozolomide. * Determine the objective response (confirmed and unconfirmed complete response and partial response) in patients with measurable disease treated with this regimen. * Determine the overall survival of patients treated with this regimen. * Determine the qualitative and quantitative toxic effects of this regimen in these patients. OUTLINE: This is a multicenter study. Patients receive oral thalidomide once daily on days 1-56 and temozolomide once daily on days 1-42. Courses repeat every 56 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed at week 9, every 2 months until disease progression, and then every 6 months until 3 years from study entry. PROJECTED ACCRUAL: A total of 55 patients will be accrued for this study within 14 months.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
64
75 mg/m\^2/day PO daily for 6 weeks followed by a 2-week break
200 mg/day PO daily
Alaska Regional Hospital Cancer Center
Anchorage, Alaska, United States
Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
Little Rock, Arkansas, United States
Eden Medical Center
Castro Valley, California, United States
North Bay Cancer Center
Fairfield, California, United States
Saint Rose Hospital
Hayward, California, United States
Progression-free survival at 6 months
Time frame: 6 months after registration
Objective response (confirmed and unconfirmed complete and partial responses)
Time frame: Week 9, every 8 weeks thereafter until progression
6-month overall survival
Time frame: six months after registration
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