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Treatment continued until PD, development of unacceptable toxicity, participant choice, withdrawal of consent or discontinuation of study by the sponsor, whichever occurred first.","id":"EG000","otherNumAffected":38,"otherNumAtRisk":39,"seriousNumAffected":30,"seriousNumAtRisk":39,"title":"Treatment Arm A: Lenvatinib + Ifosfamide + Etoposide"},{"deathsNumAffected":25,"deathsNumAtRisk":41,"description":"Participants received ifosfamide 3000 mg/m\\^2/day, intravenously and etoposide 100 mg/m\\^2/day, intravenously on Days 1 to 3 of each 21-day cycle for up to 5 cycles. Participants who had PD per RECIST v1.1 were eligible for an optional lenvatinib treatment (14 mg/m\\^2, capsules, orally, once daily in continuous 21-day cycles until next PD, development of unacceptable toxicity, participant choice, withdrawal of consent or discontinuation of study by the sponsor, whichever occurred first) plus any remaining cycles of chemotherapy if 5 cycles were not completed prior to PD.","id":"EG001","otherNumAffected":39,"otherNumAtRisk":39,"seriousNumAffected":20,"seriousNumAtRisk":39,"title":"Treatment Arm B: Ifosfamide + Etoposide"},{"deathsNumAffected":12,"deathsNumAtRisk":16,"description":"Eligible participants from Treatment Arm B: Ifosfamide+Etoposide who had PD per RECIST v1.1 received an optional lenvatinib treatment (14 mg/m\\^2, capsules, orally, once daily in continuous 21-day cycles until next PD, development of unacceptable toxicity, participant choice, withdrawal of consent or discontinuation of study by the sponsor, whichever occurred first) plus any remaining cycles of chemotherapy if 5 cycles were not completed prior to PD.","id":"EG002","otherNumAffected":16,"otherNumAtRisk":16,"seriousNumAffected":10,"seriousNumAtRisk":16,"title":"Treatment Arm B: Ifosfamide+Etoposide to Lenvatinib (Optional)"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 25.0","stats":[{"groupId":"EG000","numAffected":28,"numAtRisk":39,"numEvents":180},{"groupId":"EG001","numAffected":27,"numAtRisk":39,"numEvents":102},{"groupId":"EG002","numAffected":2,"numAtRisk":16,"numEvents":10}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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