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disorders","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":13},{"groupId":"EG002","numAffected":3,"numAtRisk":44},{"groupId":"EG003","numAffected":0,"numAtRisk":46}],"term":"Hypotension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":13},{"groupId":"EG002","numAffected":5,"numAtRisk":44},{"groupId":"EG003","numAffected":2,"numAtRisk":46}],"term":"Thromboembolic event"}],"timeFrame":"For phase I patients, adverse assessment is repeated weekly during first cycle (1 cycle = 21 days), then every cycle until patient is off protocol treatment. For phase II patients, adverse assessment is repeated every cycle until patient is off protocol treatment, up to 3 years."}