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Alternatively, if an early efficacy of the study is noted by the data monitoring committee, crossover would be considered for all participants who randomized into the docetaxel arm (so that they are able to immediately receive AMG 510).","id":"EG000","otherNumAffected":129,"otherNumAtRisk":151,"seriousNumAffected":67,"seriousNumAtRisk":151,"title":"Docetaxel"},{"deathsNumAffected":109,"deathsNumAtRisk":171,"description":"Participants with previously treated locally advanced and unresectable or metastatic non small cell lung cancer (NSCLC) with centrally confirmed Kirsten rat sarcoma viral oncogene homolog (KRAS) p.G12C mutation received 960 mg of AMG 510 orally via tablets once a day (QD) in each 21 day cycle.","id":"EG001","otherNumAffected":151,"otherNumAtRisk":169,"seriousNumAffected":91,"seriousNumAtRisk":169,"title":"AMG 510"},{"deathsNumAffected":17,"deathsNumAtRisk":46,"description":"Participants who were randomized to originally receive docetaxel, who were determined to have radiological progression according to RECIST v1.1 by the investigator and progressive disease confirmed by independent central imaging review, and switched to receive AMG 510. Alternatively, participants could switch from docetaxel to receive AMG 510 if an early efficacy of the study is noted by the data monitoring committee.","id":"EG002","otherNumAffected":35,"otherNumAtRisk":46,"seriousNumAffected":26,"seriousNumAtRisk":46,"title":"Docetaxel, Then Switched to AMG 510"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 25.0","stats":[{"groupId":"EG000","numAffected":30,"numAtRisk":151},{"groupId":"EG001","numAffected":28,"numAtRisk":169},{"groupId":"EG002","numAffected":5,"numAtRisk":46}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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