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circumstances","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":21},{"groupId":"EG001","numAffected":0,"numAtRisk":19},{"groupId":"EG002","numAffected":0,"numAtRisk":40},{"groupId":"EG003","numAffected":0,"numAtRisk":218},{"groupId":"EG004","numAffected":2,"numAtRisk":222}],"term":"Social circumstances - Other specify"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":21},{"groupId":"EG001","numAffected":0,"numAtRisk":19},{"groupId":"EG002","numAffected":0,"numAtRisk":40},{"groupId":"EG003","numAffected":0,"numAtRisk":218},{"groupId":"EG004","numAffected":1,"numAtRisk":222}],"term":"Hematoma"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":21},{"groupId":"EG001","numAffected":0,"numAtRisk":19},{"groupId":"EG002","numAffected":0,"numAtRisk":40},{"groupId":"EG003","numAffected":0,"numAtRisk":218},{"groupId":"EG004","numAffected":1,"numAtRisk":222}],"term":"Hypertension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":21},{"groupId":"EG001","numAffected":0,"numAtRisk":19},{"groupId":"EG002","numAffected":0,"numAtRisk":40},{"groupId":"EG003","numAffected":0,"numAtRisk":218},{"groupId":"EG004","numAffected":1,"numAtRisk":222}],"term":"Hypotension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":21},{"groupId":"EG001","numAffected":0,"numAtRisk":19},{"groupId":"EG002","numAffected":0,"numAtRisk":40},{"groupId":"EG003","numAffected":5,"numAtRisk":218},{"groupId":"EG004","numAffected":5,"numAtRisk":222}],"term":"Thromboembolic event"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":21},{"groupId":"EG001","numAffected":0,"numAtRisk":19},{"groupId":"EG002","numAffected":0,"numAtRisk":40},{"groupId":"EG003","numAffected":0,"numAtRisk":218},{"groupId":"EG004","numAffected":2,"numAtRisk":222}],"term":"Vasculitis"}],"timeFrame":"Adverse events were monitored continuously throughout the study and during follow-up. Patients were evaluated before each cycle, 4 weeks after discontinuation, every 12 weeks until progression, and then every 24 weeks until death, an average of 16.2 months."}