{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"26.3","upperLimit":"46.1","value":"36.2"},{"groupId":"OG001","lowerLimit":"58.6","upperLimit":"77.7","value":"68.1"}]}],"title":"EFS Rate at 6 months"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"13.9","upperLimit":"31.3","value":"22.6"},{"groupId":"OG001","lowerLimit":"46.8","upperLimit":"67.2","value":"57.0"}]}],"title":"EFS Rate at 12 months"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"13.9","upperLimit":"31.3","value":"22.6"},{"groupId":"OG001","lowerLimit":"42.3","upperLimit":"62.8","value":"52.6"}]}],"title":"EFS Rate at 18 months"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"13.0","upperLimit":"30.0","value":"21.5"},{"groupId":"OG001","lowerLimit":"41.1","upperLimit":"61.7","value":"51.4"}]}],"title":"EFS Rate at 24 months"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"11.0","upperLimit":"27.3","value":"19.1"},{"groupId":"OG001","lowerLimit":"35.2","upperLimit":"56.5","value":"45.8"}]}],"title":"EFS Rate at 36 months"}],"denoms":[{"counts":[{"groupId":"OG000","value":"92"},{"groupId":"OG001","value":"92"}],"units":"Participants"}],"description":"EFS rate is defined as the percentage of participants free of any EFS event at fixed timepoints. Complete response: Target nodes masses must regress to ≤ 1.5cm in LDi, no extralymphatic sites, no new lesions. Partial response: ≥ 50% decrease in sum of diameters of up to 6 target nodes and extranodal sites, no new lesions, spleen must have regressed \\> 50% in length. Progression: LDi \\> 1.5cm, increase by ≥ 50% from PPD nadir, an increase in LDi or SDi from nadir, 0.5 cm for lesions ≤ 2cm, 1.0cm for lesions \\> 2cm. Complete metabolic response: Lymph nodes score 1, 2, 3 with/without residual mass on 5-point scale, no new lesions, no FDG-avid disease. Partial metabolic response: Lymph nodes score 4 or 5, reduced uptake from baseline, no new lesions, residual uptake higher than normal, reduced from baseline. Metabolic progression: Score 4 or 5 with an increase in uptake intensity from baseline and/or new FDG-avid.","dispersionType":"95% Confidence Interval","groups":[{"description":"3 cycles of standard of care (SOC) salvage therapy (R-DHAP, R-ICE and R-GDP) per physician's choice. Participants responding to SOC are expected to undergo high dose chemotherapy (HDCT) and hematopoietic stem cell transplant (HSCT). If requested by the investigator, participants may be allowed to receive JCAR017 upon meeting progression, relapse, or suboptimal response. 1 cycle = 3 weeks","id":"OG000","title":"Standard of Care Arm"},{"description":"\\[Lymphodepleting chemotherapy (LDC)\\] Fludarabine IV (30 mg/m\\^2/day for 3 days) and cyclophosphamide IV (300 mg/m\\^2/day for 3 days) followed by JCAR017 IV infusion at a dose of 100 x 10\\^6 JCAR017-positive viable transduced T cells (CAR+ T cells) on Day 29 (2 to 7 days after completion of LD chemotherapy)","id":"OG001","title":"Liso-cel Arm"}],"paramType":"NUMBER","populationDescription":"All randomized participants","reportingStatus":"POSTED","timeFrame":"Months 6, 12, 18, 24, 36","title":"Event-free Survival (EFS) Rate","type":"SECONDARY","unitOfMeasure":"Percentage of participants"}