{"description":"One participant was randomized to Panitumumab Plus FOLFIRI, but received FOLFIRI Alone and is included in the FOLFIRI Alone group for safety analyses.\n\nThe table of Other Adverse Events summarizes the most frequent non-serious occurrences of adverse events.","eventGroups":[{"description":"Participants received 6 mg/kg panitumumab IV plus a standard chemotherapy regimen (FOLFIRI) consisting of 5-FU, leucovorin and irinotecan. 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