{"description":"All participants who received at least one dose of the study drug. Gender specific events occurring only in male or female participants have had the number of participants at risk adjusted accordingly. The adverse events were analyzed and reported according to the study treatments pre-specified in the protocol.","eventGroups":[{"deathsNumAffected":1,"deathsNumAtRisk":7,"description":"Participants received:\n\n* Abemaciclib: 70 mg/m², administered orally twice daily (BID).\n* Irinotecan: 50 mg/m²/day, administered IV on Days 1-5 of each cycle.\n* Temozolomide: 100 mg/m²/day, administered orally on Days 1-5 of each cycle.\n\nTreatment continued until progressive disease, a discontinuation criterion, or unacceptable toxicity. Each cycle lasted 21 days.","id":"EG000","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":3,"seriousNumAtRisk":7,"title":"Part A Cohort A1"},{"deathsNumAffected":1,"deathsNumAtRisk":13,"description":"Participants received:\n\n* Abemaciclib: 55 mg/m², administered orally BID.\n* Irinotecan: 50 mg/m²/day, administered IV on Days 1-5 of each cycle.\n* Temozolomide: 100 mg/m²/day, administered orally on Days 1-5 of each cycle.\n\nTreatment continued until progressive disease, a discontinuation criterion, or unacceptable toxicity. Each cycle lasted 21 days.","id":"EG001","otherNumAffected":13,"otherNumAtRisk":13,"seriousNumAffected":5,"seriousNumAtRisk":13,"title":"Part A Cohort A-1"},{"deathsNumAffected":0,"deathsNumAtRisk":3,"description":"Participants received:\n\n* Abemaciclib: 70 mg/m², administered orally BID.\n* Temozolomide: 100 mg/m²/day, administered orally on Days 1-5 of each cycle.\n\nTreatment continued until progressive disease, a discontinuation criterion, or unacceptable toxicity. Each cycle lasted 21 days.","id":"EG002","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":2,"seriousNumAtRisk":3,"title":"Part B Cohort B1"},{"deathsNumAffected":1,"deathsNumAtRisk":9,"description":"Participants received:\n\n* Abemaciclib: 90 mg/m², administered orally BID.\n* Temozolomide: 100 mg/m²/day, administered orally on Days 1-5 of each cycle.\n\nTreatment continued until progressive disease, a discontinuation criterion, or unacceptable toxicity. Each cycle lasted 21 days.","id":"EG003","otherNumAffected":8,"otherNumAtRisk":9,"seriousNumAffected":0,"seriousNumAtRisk":9,"title":"Part B Cohort B2"},{"deathsNumAffected":1,"deathsNumAtRisk":3,"description":"Participants received:\n\n* Abemaciclib: 115 mg/m², administered orally BID.\n* Temozolomide: 100 mg/m²/day, administered orally on Days 1-5 of each cycle.\n\nTreatment continued until progressive disease, a discontinuation criterion, or unacceptable toxicity. Each cycle lasted 21 days.","id":"EG004","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":0,"seriousNumAtRisk":3,"title":"Part B Cohort B3"},{"deathsNumAffected":2,"deathsNumAtRisk":11,"description":"Participants received:\n\n* Abemaciclib: 115 mg/m², administered orally BID.\n* Temozolomide: 150 mg/m²/day, administered orally on Days 1-5 of each cycle.\n\nTreatment continued until progressive disease, a discontinuation criterion, or unacceptable toxicity. Each cycle lasted 21 days.","id":"EG005","otherNumAffected":11,"otherNumAtRisk":11,"seriousNumAffected":4,"seriousNumAtRisk":11,"title":"Part B Cohort B5"},{"deathsNumAffected":0,"deathsNumAtRisk":1,"description":"Participants received:\n\n* Abemaciclib: 55 mg/m², administered orally BID.\n* Irinotecan: 50 mg/m²/day, administered IV on Days 1-5 of each cycle.\n* Temozolomide: 100 mg/m²/day, administered orally on Days 1-5 of each cycle.\n* Dinutuximab: 17.5mg/m²/day, administered IV on Days 2-5 of each cycle.\n* Granulocyte-macrophage colony-stimulating factor (GM-CSF): 250 μg/m²/day, administered subcutaneously (SC) on Days 6-12 of each cycle.\n\nTreatment continued until progressive disease, a discontinuation criterion, or unacceptable toxicity. Each cycle lasted 21 days.","id":"EG006","otherNumAffected":1,"otherNumAtRisk":1,"seriousNumAffected":1,"seriousNumAtRisk":1,"title":"Part C Cohort C1"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.0","stats":[{"groupId":"EG000","numAffected":5,"numAtRisk":7,"numEvents":11},{"groupId":"EG001","numAffected":8,"numAtRisk":13,"numEvents":17},{"groupId":"EG002","numAffected":1,"numAtRisk":3,"numEvents":1},{"groupId":"EG003","numAffected":5,"numAtRisk":9,"numEvents":5},{"groupId":"EG004","numAffected":2,"numAtRisk":3,"numEvents":3},{"groupId":"EG005","numAffected":7,"numAtRisk":11,"numEvents":15},{"groupId":"EG006","numAffected":1,"numAtRisk":1,"numEvents":3}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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