Uveal melanoma arises from melanocytes within the choroid of the eye, has an incidence of 1500 cases per year in the United States, and is biologically distinct from cutaneous melanoma.
1,2 Despite enucleation or definitive radiotherapy of the primary lesion, metastases develop in 50% of patients and outcomes are subsequently poor, with a median survival of less than 12 months.
3-5 Although improved outcomes have been achieved in patients with advanced cutaneous melanoma, no effective therapy has been identified for those with metastatic uveal melanoma.