{"description":"The toxicity profile will be described by specific adverse event rates among patients experiencing \\> grade 3 hematologic events (lasting \\>7 days) or grades 3-5 non-hematologic adverse events, according to NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.0, over a 28 day cycle. Specific events will be described as the numbers of patients experiencing them within each treatment cohort.","reportingStatus":"NOT_POSTED","timeFrame":"2 years","title":"Toxicity Profile","type":"SECONDARY"}