In the Belatacept Evaluation of Nephroprotection and Efficacy as FirstâLine Immunosuppression TrialâExtended Criteria Donors (BENEFITâEXT), extended criteria donor kidney recipients were randomized to receive belataceptâbased (more intense [MI] or less intense [LI]) or cyclosporineâbased immunosuppression. In prior analyses, belatacept was associated with significantly better renal function compared with cyclosporine. In this prospective analysis of the intentâtoâtreat population, efficacy and safety were compared across regimens at 7 years after transplant. Overall, 128 of 184 belatacept MIâtreated, 138 of 175 belatacept LIâtreated and 108 of 184 cyclosporineâtreated patients contributed data to these analyses. Hazard ratios (HRs) comparing time to death or graft loss were 0.915 (95% confidence interval [CI] 0.625â1.339; p = 0.65) for belatacept MI versus cyclosporine and 0.927 (95% CI 0.634â1.356; p = 0.70) for belatacept LI versus cyclosporine. Mean estimated GFR (eGFR) plus or minus standard error at 7 years was 53.9 ± 1.9, 54.2 ± 1.9, and 35.3 ± 2.0 mL/min per 1.73 m2 for belatacept MI, belatacept LI and cyclosporine, respectively (p < 0.001 for overall treatment effect). HRs comparing freedom from death, graft loss or eGFR <20 mL/min per 1.73 m2 were 0.754 (95% CI 0.536â1.061; p = 0.10) for belatacept MI versus cyclosporine and 0.706 (95% CI 0.499â0.998; p = 0.05) for belatacept LI versus cyclosporine. Acute rejection rates and safety profiles of belataceptâ and cyclosporineâbased treatment were similar. De novo donorâspecific antibody incidence was lower for belatacept (p †0.0001). Relative to cyclosporine, belatacept was associated with similar death and graft loss and improved renal function at 7 years after transplant and had a safety profile consistent with previous reports.