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19.1","stats":[{"groupId":"EG000","numAffected":3,"numAtRisk":157,"numEvents":3},{"groupId":"EG001","numAffected":2,"numAtRisk":55,"numEvents":2},{"groupId":"EG002","numAffected":3,"numAtRisk":119,"numEvents":3}],"term":"Myelodysplastic syndrome"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Neoplasms benign, malignant and unspecified (incl cysts and polyps)","sourceVocabulary":"MedDRA version 19.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":157,"numEvents":1},{"groupId":"EG001","numAffected":1,"numAtRisk":55,"numEvents":1},{"groupId":"EG002","numAffected":1,"numAtRisk":119,"numEvents":1}],"term":"Refractory cytopenia with multilineage dysplasia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Nervous system disorders","sourceVocabulary":"MedDRA version 19.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":157,"numEvents":1},{"groupId":"EG001","numAffected":0,"numAtRisk":55,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":119,"numEvents":0}],"term":"Peripheral sensory neuropathy"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Nervous system disorders","sourceVocabulary":"MedDRA version 19.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":157,"numEvents":1},{"groupId":"EG001","numAffected":0,"numAtRisk":55,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":119,"numEvents":0}],"term":"Cerecrovascular accident"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Psychiatric disorders","sourceVocabulary":"MedDRA version 19.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":157,"numEvents":1},{"groupId":"EG001","numAffected":1,"numAtRisk":55,"numEvents":1},{"groupId":"EG002","numAffected":0,"numAtRisk":119,"numEvents":0}],"term":"Mental status changes"}],"timeFrame":"Patients were treated in 28 day cycles indefinitely until withdrawal from study, with the longest time on study of 17 months. Adverse events were collected until 30 days after the last dose of study drug. Patients were followed for survival for 24 months after disease progression or start of subsequent anti-myeloma therapy."}