{"description":"All patients enrolled were included in the all-cause mortality analysis. Forty-three patients were included in the toxicity analysis (excluding one who did not receive treatment).","eventGroups":[{"deathsNumAffected":24,"deathsNumAtRisk":44,"description":"Patients receive dabrafenib mesylate 150 mg PO BID and trametinib dimethyl sulfoxide 2 mg PO QD on days 1-28. 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