Clinical Trial of Sutent to Treat Metastatic Melanoma

Exclusion Criteria

• •Major surgery or radiation therapy within 2 weeks of starting the study treatment. Prior palliative radiotherapy to metastatic lesion(s) is permitted, provided there is at least one measurable lesion that has not been irradiated.
• •NCI CTCAE Version 3.0 grade 3 hemorrhage within 4 weeks of starting the study treatment.
• •Diagnosis of any second malignancy within the last 2 years, except for adequately treated basal cell carcinoma, squamous cell skin cancer, localized prostate cancer, or in situ cervical cancer.
• •Active brain metastases, spinal cord compression, or evidence of symptomatic brain or leptomeningeal carcinomatosis on screening CT or MRI scan. Patients who have had central nervous system metastases treated by surgery or radiation therapy and with those CNS metastases considered in control will be eligible, provided measurable disease outside the CNS is present.
• •Any of the following within the 2 months prior to study drug administration: myocardial infarction, severe/unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, or pulmonary embolism.
• •Ongoing cardiac dysrhythmias of NCI CTCAE Version 3.0 grade \> 2.
• •Prolonged QTc interval on baseline EKG (\>450 msec for males or \>470 msec for females)
• •Uncontrolled hypertension (\> 160/100 mm hg despite optimal medical therapy).
• •Concurrent treatment on another clinical trial. Supportive care trials or non-treatment trials, e.g., QOL, are allowed.
• •Ongoing treatment with therapeutic doses of warfarin (low dose warfarin up to 2 mg po daily for thromboprophylaxis is allowed).
• •Pregnant or breastfeeding.
• •Life expectancy less than 3 months.