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Following the primary analysis, the study was transitioned to an open-label extension (OLE) phase, and participants either continued to receive the chemotherapy or crossover to amivantamab in the OLE phase.","id":"EG000","otherNumAffected":149,"otherNumAtRisk":155,"seriousNumAffected":48,"seriousNumAtRisk":155,"title":"Arm B: Chemotherapy Alone"},{"deathsNumAffected":28,"deathsNumAtRisk":151,"description":"Participants received amivantamab 1400 milligrams (mg) (1750 mg if body weight is greater than or equal to (\\>=) 80 kilograms \\[kg\\]) by IV infusion once weekly starting from Cycle 1 Day 1 up to Cycle 2 Day 1, then 1750 mg (2100 mg if body weight is \\>=80 kg) on Day 1 of each 21-day cycle, starting with Cycle 3 up to Cycle 5 Day 1. Participants received chemotherapy with pemetrexed 500 mg/m\\^2 IV infusion (with vitamin supplementation) on Day 1 of each 21-day cycle, in combination with carboplatin area under the concentration-time curve of 5 milligrams per milliliter (mg/mL) per minute (AUC 5) was administered as an IV infusion on Day 1, for up to 4 cycles, and then as maintenance monotherapy until disease progression. Following the primary analysis, the study was transitioned to an OLE phase, and participants continued to receive amivantamab plus chemotherapy in the OLE phase.","id":"EG001","otherNumAffected":151,"otherNumAtRisk":151,"seriousNumAffected":56,"seriousNumAtRisk":151,"title":"Arm A: Amivantamab + Chemotherapy"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Skin and subcutaneous tissue disorders","sourceVocabulary":"MedDRA Version 25.0","stats":[{"groupId":"EG000","numAffected":12,"numAtRisk":155},{"groupId":"EG001","numAffected":81,"numAtRisk":151}],"term":"Rash"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Skin and subcutaneous tissue disorders","sourceVocabulary":"MedDRA Version 25.0","stats":[{"groupId":"EG000","numAffected":5,"numAtRisk":155},{"groupId":"EG001","numAffected":47,"numAtRisk":151}],"term":"Dermatitis Acneiform"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Skin and subcutaneous 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