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      A prolonged complete response in a patient with BRAF-mutated melanoma stage IV treated with the MEK1/2 inhibitor selumetinib (AZD6244).

      Anti-Cancer Drugs
      Adult, Antineoplastic Agents, therapeutic use, Benzimidazoles, Disease-Free Survival, Female, Head and Neck Neoplasms, drug therapy, genetics, Humans, MAP Kinase Kinase 1, antagonists & inhibitors, MAP Kinase Kinase 2, Melanoma, Proto-Oncogene Proteins B-raf, Skin Neoplasms, Thoracic Neoplasms, secondary

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          Abstract

          In melanoma, the RAS/RAF/MEK/ERK pathway is frequently activated by mutations in BRAF and NRAS. Selumetinib (AZD6244) is an oral, selective, non-ATP-competitive inhibitor of MEK1/2. Here, we describe a patient with metastatic melanoma (T1N2cM1a) with a BRAF V600E mutation. She is currently being treated with selumetinib 75 mg twice daily in a phase I trial and has shown complete response for the past 4 years. This case report raises questions regarding treatment schedule, treatment duration and management of adverse events.

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